Northwest Clinical Genomics Laboratory

Test NamePanelDisease NameGeneLaboratoryCPT Code
Cardiac Arrhythmia PanelYesCardiac Arrhythmia
ABCC9, ANK2, CACNA1C, CACNA1D, CACNB2, CALM1, CALM2, CASQ2, CAV3, DES, DPP6, DSC2, DSG2, DSP, EMD, GJA5, GLA, GNAI2, GPD1L, HCN4, KCNA5, KCND3, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, LDB3, LMNA, MYH6, NKX2-5, NPPA, PKP2, PLN, PRKAG2, RBM20, RYR2, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SNTA1, TMEM43, TNNT2, TRDN, TRPM4, TTN
Northwest Clinical Genomics Lab 81413
Cardiomyopathy PanelYesCardiomyopathy
ABCC9, ACTC1, ACTN2, ANKRD1, BAG3, BRAF, CASQ2, CAV3, CBL, CHRM2, CRYAB, CSRP3, DES, DMD, DOLK, DSC2, DSG2, DSP, DTNA, EMD, FHL2, FKTN, GAA, GATAD1, GLA, HRAS, ILK, JPH2, JUP, KRAS, LAMA4, LAMP2, LDB3, LMNA, MAP2K1, MAP2K2, MURC, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, MYPN, NEBL, NEXN, NRAS, PDLIM3, PKP2, PLN, PRDM16, PRKAG2, PSEN1, PSEN2, PTPN11, RAF1, RBM20, RIT1, RYR2, SCN5A, SGCD, SHOC2, SOS1, TAZ, TCAP, TMEM43, TMPO, TNNC1, TNNI3, TNNT2, TPM1, TRDN, TTN, TTR, VCL
Northwest Clinical Genomics Lab 81439
Comprehensive Cardiac Arrhythmia/Cardiomyopathy PanelYesCardiac Arrhythmia and/or Cardiomyopathy
ABCC9, ACTC1, ACTN2, ANK2, ANKRD1, BAG3, BRAF, CACNA1C, CACNA1D, CACNB2, CALM1, CALM2, CASQ2, CAV3, CBL, CHRM2, CRYAB, CSRP3, DES, DMD, DOLK, DPP6, DSC2, DSG2, DSP, DTNA, EMD, FHL2, FKTN, GAA, GATAD1, GJA5, GLA, GNAI2, GPD1L, HCN4, HRAS, ILK, JPH2, JUP, KCNA5, KCND3, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, KRAS, LAMA4, LAMP2, LDB3, LMNA, MAP2K1, MAP2K2, MURC, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, MYPN, NEBL, NEXN, NKX2-5, NPPA, NRAS, PDLIM3, PKP2, PLN, PRDM16, PRKAG2, PSEN1, PSEN2, PTPN11, RAF1, RBM20, RIT1, RYR2, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SGCD, SHOC2, SNTA1, SOS1, TAZ, TCAP, TMEM43, TMPO, TNNC1, TNNI3, TNNT2, TRDN, TRPM4, TTN, TTR, VCL
Northwest Clinical Genomics Lab 81479
Exome SequencingPossible Genetic Disorder
Coding sequence of the genome
Northwest Clinical Genomics Lab 81415 Proband 81416 Comparator
Exome Sequencing Re-analysisPossible Genetic Disorder
Coding sequence of the genome
Northwest Clinical Genomics Lab 81417
Genome SequencingPossible Genetic Disorder
Whole Genome Sequence
Northwest Clinical Genomics Lab 81425 Proband 81426 Comparator
Genome Sequencing Re-analysisPossible Genetic Disorder
Whole Genome Sequence
Northwest Clinical Genomics Lab 81427
Movement Disorder PanelsYesHeritable Movement Disorders
ABCB7, ABCD1, ABHD12, ACAT1, ACOX1, ACTB, ACVR1, ADAR, ADCK3, ADCY5, ADD3, ADGRG1, AFG3L2, AHI1, ALAS2, ALDH5A1, ALG6, ALS2, AMACR, AMPD2, ANG, ANO10, ANO3, ANO5, AP1S2, AP4B1, AP4E1, AP4M1, AP4S1, AP5Z1, APTX, ARHGEF28, ARL13B, ARL6, ARL6IP1, ARSA, ARSI, ARX, ASAH1, ATCAY, ATL1, ATM, ATP13A2, ATP1A2, ATP1A3, ATP6AP2, ATP7A, ATP7B, ATP8A2, AUH, B4GALNT1, BAG3, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BCAP31, BEAN1, BICD2, BIN1, BSCL2, BTD, C10orf2, C12orf65, C19orf12, C5orf42, CA8, CACNA1A, CACNB4, CAMTA1, CASQ1, CAV3, CC2D2A, CCDC28B, CCDC78, CCDC88C, CCT5, CEP290, CEP41, CFL2, CHCHD10, CHMP2B, CIZ1, CLCN2, CLN3, CLN5, CLPP, CNTN1, COL12A1, COL6A1, COL6A2, COL6A3, COMT, COX20, CP, CRAT, CRYAB, CSF1R, CSTB, CTC1, CTSD, CWF19L1, CYP27A1, CYP2U1, CYP7B1, DARS2, DCAF17, DCTN1, DDB2, DDC, DDHD1, DDHD2, DES, DLAT, DNA2, DNAJC13, DNAJC19, DNAJC3, DNAJC5, DNAJC6, DNM2, DNMT1, DRD2, DRD5, DYSF, DYT1, EARS2, EEF2, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, EIF4G1, ELOVL4, ELOVL5, ENTPD1, EPM2A, ERCC2, ERCC3, ERCC4, ERCC5, ERCC6, ERLIN2, FA2H, FASTKD2, FBXL4, FBXO7, FGF14, FHL1, FKBP14, FLNC, FLRT1, FLVCR1, FOXG1, FOXRED1, FTL, FUS, GAD1, GALC, GAMT, GAN, GARS, GBA, GBA2, GBE1, GCDH, GCH1, GCLC, GFAP, GIGYF2, GJA1, GJB1, GJC2, GLB1, GNAL, GNE, GOSR2, GRID2, GRM1, HACD1, HARS, HEPACAM, HEXA, HEXB, HNRNPA1, HNRNPA2B1, HPRT1, HSPB1, HSPB3, HSPB8, HSPD1, HTRA2, IGHMBP2, ISCU, ITM2B, ITPR1, KANK1, KBTBD13, KCNA1, KCNC3, KCND3, KCNJ10, KCNMA1, KCNQ2, KDM5C, KIAA0196, KIF1A, KIF1C, KIF5C, KIF7, KLHL40, KLHL41, KLHL9, L2HGDH, LAMP2, LARS2, LDB3, LMNB1, LMOD3, LRRK2, LYST, MAG, MAPT, MARS, MARS2, MAT1A, MATR3, MCOLN1, MECP2, MEGF10, MKKS, MKS1, MLC1, MMADHC, MPV17, MR1, MRE11A, MSTN, MTHFR, MTM1, MTMR14, MTPAP, MYF6, MYH14, MYH2, MYH7, MYOT, NDUFV1, NEB, NEDD4, NEFH, NEU1, NHLRC1, NIPA1, NKX2-1, NOL3, NOP56, NPC1, NPC2, NPHP1, NT5C2, OFD1, OPA1, OPA3, OPTN, PABPN1, PANK2, PARK2, PARK7, PAX6, PDGFB, PDGFRB, PDHX, PDSS1, PDSS2, PEX10, PEX2, PEX7, PFN1, PGAP1, PHYH, PIK3R5, PINK1, PLA2G6, PLEC, PLEKHG4, PLEKHG5, PLP1, PMM2, PMPCA, PNKD, PNKP, PNPLA6, PNPT1, POLG, POLG2, POLH, PPP2R2B, PQBP1, PRICKLE1, PRKCG, PRKRA, PRNP, PRPH, PRRT2, PSEN1, PTEN, PTS, QDPR, RAB29, RAB39B, RAB3GAP1, RAB3GAP2, RARS2, REEP1, REEP2, RELN, RNASEH2A, RNASEH2B, RNASEH2C, RNF170, RNF216, RPGRIP1L, RRM2B, RTN2, RUBCN, RYR1, SACS, SAMD9L, SAMHD1, SCN8A, SCO2, SCP2, SDHAF1, SERAC1, SETX, SGCE, SIGMAR1, SIL1, SLC16A2, SLC17A5, SLC19A3, SLC1A3, SLC20A2, SLC25A15, SLC2A1, SLC30A10, SLC33A1, SLC46A1, SLC52A2, SLC52A3, SLC5A2, SLC6A3, SMPD1, SNCA, SNX14, SOD1, SPAST, SPEG, SPG11, SPG20, SPG21, SPG7, SPR, SPTBN2, STAC3, STIM1, STUB1, STXBP1, SUCLA2, SUOX, SYNE1, SYNJ1, SYT14, TAF1, TARDBP, TBP, TCTN1, TCTN2, TCTN3, TDP1, TECPR2, TFG, TGM6, TH, THAP1, TIA1, TIMM8A, TK2, TMEM138, TMEM216, TMEM230, TMEM231, TMEM237, TMEM240, TMEM67, TNNT1, TOR1A, TPK1, TPM2, TPM3, TPP1, TREM2, TREX1, TRIM32, TRPV4, TSEN2, TSEN34, TSEN54, TTBK2, TTC8, TTN, TTPA, TTR, TUBB4A, UBA1, UBQLN2, UCHL1, USP8, VAMP1, VAPB, VCP, VEGFA, VLDLR, VMA21, VPS13A, VPS13C, VPS35, VPS37A, VPS54, VRK1, WDPCP, WDR45, WDR48, WDR81, WFS1, WWOX, XPA, XPC, YARS2, ZFR, ZFYVE26, ZFYVE27, ZNF423, ZNF592
Northwest Clinical Genomics Lab 81479
Neurodegenerative Disorder PanelsYesNeurodegenerative Disease Panel
AARS2, ABAT, ABCD1, ACAT1, ACOX1, ACTB, ACVR1, ADAR, ADCK3, ADCY5, ADK, AFG3L2, AIMP1, AIRE, ALDH3A2, ALS2, ANG, ANO3, ANO5, AP1S2, APOE, APOPT1, APP, APTX, ARHGEF28, ARSA, ARX, ASAH1, ASPA, ATM, ATP13A2, ATP1A2, ATP1A3, ATP6AP2, ATP7A, ATP7B, ATPAF2, ATXN2, AUH, B3GALNT2, BAG3, BCAP31, BCS1L, BEST1, BIN1, BRAF, C10orf2, C19orf12, CA2, CACNA1A, CASQ1, CAV3, CCDC78, CFL2, CHCHD10, CHMP2B, CIZ1, CLCN2, CLN3, CLN5, CLN6, CLN8, CNTN1, COASY, COL12A1, COL4A1, COL6A1, COL6A2, COL6A3, COMT, COQ2, COQ9, COX10, COX15, COX20, CP, CRYAB, CSF1R, CSTB, CTC1, CTSD, CTSF, CYP27A1, CYP2U1, CYP7B1, D2HGDH, DARS, DARS2, DCAF17, DCTN1, DDC, DES, DGUOK, DLAT, DNA2, DNAJC13, DNAJC5, DNAJC6, DNM2, DNMT1, DRD2, DRD5, DYSF, DYT1, EARS2, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, EIF4G1, EPM2A, ERBB4, ERCC3, ERCC6, ERCC8, ETFDH, FA2H, FAM126A, FASTKD2, FBXL4, FBXO7, FHL1, FIG4, FKBP14, FKRP, FLNC, FOLR1, FOXG1, FOXRED1, FTL, FUCA1, FUS, GALC, GAMT, GAN, GATA3, GBA, GBE1, GCDH, GCH1, GFAP, GFM1, GIGYF2, GJA1, GJC2, GLA, GLB1, GNAL, GNAQ, GNE, GOSR2, GRN, GTF2H5, HACD1, HEPACAM, HEXA, HNRNPA1, HNRNPA2B1, HPRT1, HSD17B4, HSPD1, HTRA1, HTRA2, HTT, ISCU, ITM2B, KBTBD13, KCNMA1, KCNQ2, KCNT1, KCTD7, KIF1C, KLHL40, KLHL41, KLHL9, L2HGDH, LAMP2, LDB3, LMNB1, LMOD3, LRRK2, MAPT, MARS2, MAT1A, MATR3, MCOLN1, MECP2, MEGF10, MFSD8, MLC1, MLYCD, MMADHC, MPLKIP, MPV17, MR1, MRPS16, MRPS22, MSTN, MTFMT, MTM1, MTMR14, MYF6, MYH14, MYH2, MYH7, MYOT, NDUFA1, NDUFA10, NDUFA11, NDUFA12, NDUFA2, NDUFA9, NDUFAF1, NDUFAF2, NDUFAF3, NDUFAF4, NDUFAF5, NDUFAF6, NDUFB3, NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS5, NDUFS6, NDUFS7, NDUFS8, NDUFV1, NDUFV2, NDUFV3, NEB, NEFH, NEK1, NHLRC1, NKX2-1, NOTCH3, NPC1, NPC2, NUBPL, OCLN, OCRL, OPA1, OPTN, PABPN1, PAH, PANK2, PARK2, PARK7, PC, PDGFB, PDGFRB, PDHX, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, PEX7, PFN1, PHGDH, PHYH, PINK1, PLA2G6, PLEC, PLP1, PNKD, PNPT1, POLG, POLG2, POLR3A, POLR3B, PPT1, PPT2, PRF1, PRICKLE1, PRICKLE2, PRKRA, PRNP, PRPH, PRPS1, PRRT2, PSAP, PSAT1, PSEN1, PSEN2, PSMB8, PTEN, PTPN11, PTS, QDPR, RAB29, RAB39B, RAF1, RARS2, REPS1, RNASEH2A, RNASEH2B, RNASEH2C, RNASET2, ROGDI, RRM2B, RYR1, SAMHD1, SCARB2, SCO1, SCO2, SCP2, SDHA, SDHAF1, SDHB, SERAC1, SETX, SGCE, SIGMAR1, SIL1, SLC16A2, SLC17A5, SLC19A3, SLC20A2, SLC25A1, SLC25A12, SLC25A15, SLC25A4, SLC2A1, SLC30A10, SLC46A1, SLC6A3, SMPD1, SNCA, SOD1, SOX10, SPAST, SPEG, SPG11, SPG20, SPG21, SPG7, SPR, SQSTM1, SRRT, STAC3, STIM1, STX11, STXBP1, SUCLA2, SUMF1, SUOX, SURF1, SYNJ1, TACO1, TAF1, TARDBP, TARS2, TBK1, TBP, TH, THAP1, TIA1, TIMM8A, TK2, TMEM230, TNNT1, TOR1A, TPK1, TPM2, TPM3, TPP1, TREM2, TREX1, TRIM32, TTC3, TTN, TUBB4A, TUFM, TYMP, TYROBP, UBQLN2, UCHL1, UNC13D, VAPB, VARS, VCP, VEGFA, VMA21, VPS13A, VPS13C, VPS35, VPS37A, VPS54, WDR45, YARS2, ZFYVE26, ZNF592
Northwest Clinical Genomics Lab 81479
Neuromuscular Disorder PanelsYesHeritable Neuromuscular Disorders
AARS, ABHD12, ABHD5, ACAD9, ACADL, ACADM, ACADS, ACADVL, ACTA1, ACVR1, ADCY6, AGL, AGRN, AIFM1, ALG13, ALG14, ALG2, AMPD1, ANO5, ARHGEF10, ASAH1, ATL1, ATL3, ATP2A1, ATP7A, B3GALNT2, B4GAT1, BAG3, BICD2, BIN1, BSCL2, C10orf2, C12orf65, CAPN3, CASQ1, CAV3, CCDC78, CCT5, CFL2, CHAT, CHCHD10, CHKB, CHRNA1, CHRNB1, CHRND, CHRNE, CHRNG, CHST14, CLCN1, CNTN1, CNTNAP1, COL12A1, COL4A1, COL6A1, COL6A2, COL6A3, COLQ, COX6A1, CPT2, CRYAB, CTDP1, DAG1, DCAF8, DCTN1, DES, DHTKD1, DMD, DNA2, DNAJB2, DNAJB6, DNM2, DNMT1, DOK7, DPAGT1, DPM2, DPM3, DST, DYNC1H1, DYSF, ECEL1, EGR2, EMD, ENO3, ERBB3, ETFA, ETFB, ETFDH, FAM134B, FBLN5, FBN2, FBXO38, FGD4, FHL1, FIG4, FKBP10, FKBP14, FKRP, FKTN, FLNC, FUS, GAA, GAN, GARS, GBE1, GDAP1, GFPT1, GJB1, GLE1, GMPPB, GNB4, GNE, GYG1, GYS1, HACD1, HADH, HADHA, HADHB, HARS, HINT1, HK1, HNRNPA1, HNRNPA2B1, HNRNPDL, HOXD10, HSPB1, HSPB3, HSPB8, IGHMBP2, IKBKAP, INF2, ISCU, ISPD, ITGA7, KARS, KBTBD13, KIF1A, KIF1B, KIF5A, KLHL40, KLHL41, KLHL9, LAMA2, LAMC1, LAMP2, LARGE, LAS1L, LDB3, LDHA, LITAF, LMNA, LMOD3, LPIN1, LRP4, LRSAM1, MARS, MATR3, MED25, MEGF10, MFN2, MPZ, MSTN, MTM1, MTMR14, MTMR2, MUSK, MYBPC1, MYF6, MYH14, MYH2, MYH3, MYH8, MYOT, NALCN, NDRG1, NEB, NEFL, NGF, NTRK1, OPA1, ORAI1, PABPN1, PDHA1, PDK3, PFKM, PGAM2, PGK1, PGM1, PHKA1, PHKB, PIEZO2, PIP5K1C, PLEC, PLEKHG5, PLOD2, PMP22, PNPLA2, POLG, POLG2, POMGNT1, POMGNT2, POMK, POMT1, POMT2, PREPL, PRPS1, PRX, PTRF, PUS1, PYGM, RAB7A, RAPSN, RBCK1, REEP1, RRM2B, RYR1, SBF1, SBF2, SCN10A, SCN11A, SCN4A, SCN9A, SCO2, SEPN1, SEPT9, SGCA, SGCB, SGCD, SGCG, SH3TC2, SIL1, SLC12A6, SLC16A1, SLC22A5, SLC25A20, SLC5A7, SMCHD1, SNAP25, SOX10, SPEG, SPTLC1, SPTLC2, STAC3, STIM1, SUCLA2, SURF1, SYNE1, SYNE2, SYT2, TAZ, TCAP, TFG, TIA1, TK2, TMEM43, TMEM5, TNNI2, TNNT1, TNNT3, TNPO3, TPM2, TPM3, TRAPPC11, TRIM2, TRIM32, TRPV4, TTN, TTR, TUBB3, TYMP, UBA1, VAPB, VCP, VMA21, VRK1, WNK1, YARS, YARS2, ZC4H2
Northwest Clinical Genomics Lab 81479
Panel on DemandYesPossible Genetic Disorder
Selected genes
Northwest Clinical Genomics Lab 81479
REFLEX to Exome SequencingPossible genetic disorder
Coding sequence of the genome
Northwest Clinical Genomics Lab 81417
Retinal Dystrophy PanelYesRetinal Dystrophy
ABCA4, ABCC6, ABCD1, ABHD12, ACBD5, ACO2, ADAM9, ADAMTS18, AHI1, AIPL1, ALMS1, AMACR, ARL13B, ARL2BP, ARL3, ARL6, ATF6, B9D1, B9D2, BBIP1, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BEST1, C12orf65, C1orf71 (CNST), C1QTNF5, C21orf2, C2orf71, C5orf42, C8orf37, CA4, CABP4, CACNA1F, CACNA2D4, CC2D2A, CDH15, CDH23, CDH3, CDHR1, CEP164, CEP250, CEP290 (BBS14), CEP41, CERKL, CFH, CHM, CIB2, CISD2, CKAP4, CLN14, CLN3, CLN5, CLN6, CLN8, CLRN1, CNGA1, CNGA3, CNGB1, CNGB3, CNNM4, COH1 (VPS13B), CRB1, CRX, CSPP1, CTNNA1, CTSD, CTSF, CYP4V2, DFNB31, DGKQOAT, DHDDS, DHX38, DNAJC5, DRAM2, DTHD1, EFEMP1, ELOVL4, EMC1, EYS, FAM161A, FLVCR1, FSCN2, FZD4, GDF6, GJB2, GJB6, GNAT1, GNAT2, GPR125, GPR179, GPR98 (ADGRV1), GRK1, GRM6, GRN, GUCA1A, GUCA1B, GUCY2D, HARS, HCN1, HGSNAT, HK1, HMCN1, HMX1, IDH3B, IFT140, IFT172, IFT27, IFT81, IMPDH1, IMPG1, IMPG2, INVS, ITM2B, JAG1, KIF11, KIF7, KIZ, LAMA1, MFN2, MFSD8, MIR204, MKKS, MKS1, MMACHC, MTTP, MVK, MYO7A, NDP, NEK2, NEUROD1, NMNA, NPHP1, NPHP3, NPHP4, NR2E3, NR2F1, NRL, NYX, OFD1, OPA1, OPA3, OR2W3, OTX2, PANK2, PAX2, PCDH15, PDE6A, PDE6B, PDE6C, PDE6D, PDE6G, PDE6H, PDZD7, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, PEX7, PGK1, PHYH, PITPNM3, PLA2G5, PLK4, PMPCA, PNPLA6, POC1B, PPT1, PRCD, PRKCG, PROM1, PRPF3, PRPF31, PRPF4, PRPF6, PRPF8, PRPH2 (RDS), PRPS1, RAB28, RAX2, RBP3, RBP4, RD3, RDH11, RDH12, RDH5, RGR, RGS9, RGS9BP, RHO, RIMS1, RLBP1, ROM1, RP1, RP1L1, RP2, RP9, RPE65, RPGR, RPGRIP1, RPGRIP1L, RS1, RTN4IP1, SAB, SDCCAG8, SEMA4A, SLC24A1, SLC25A46, SLC4A7, SLC7A14, SNRNP200, SPATA7, SPP2, T1, TCTN1, TCTN2, TCTN3, TEAD1, TIMM8A, TIMP3, TMEM126A, TMEM138, TMEM216, TMEM231, TMEM237, TMEM67, TOPORS, TPP1, TREX1, TRIM32, TRNT1, TRPM1, TSPAN12, TTC21B, TTC8, TTLL10, TTLL5, TTPA, TUB, TUBGCP4, TUBGCP6, TULP1, UNC119, USH1G, USH2A, VCAN, WDPCP, WDR19, WFS1, ZNF513
Northwest Clinical Genomics Lab 81434
Testing for Known Pathogenic VariantAll diseases
All genes
Northwest Clinical Genomics Lab 81479

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