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Variant Placements (including Supporting Variants) for nstd27 (displaying 100 of 27686 variants)
Study IDVariant IDVariant Region typeVariant Call typeSampleset IDMethodAnalysis IDValidationVariant samplesSubject phenotypeClinical InterpretationAssemblyAccessionChrOuter-StartStartInner-StartInner-EndEndOuter-EndPlacement TypeRemap Score
nstd27nssv533179copy number lossSNP arraySNP genotyping analysisNo1782681247_AGRCh38.p12NC_000001.11112172511275912Remapped1
nstd27nssv533180copy number lossSNP arraySNP genotyping analysisNoHGDP00515GRCh38.p12NC_000001.11128529772912986Remapped1
nstd27nssv534983copy number lossSNP arraySNP genotyping analysisNoHGDP01234GRCh38.p12NC_000001.11131457973188066Remapped1
nstd27nssv535843copy number lossSNP arraySNP genotyping analysisNoHGDP00814GRCh38.p12NC_000001.11131671483197116Remapped1
nstd27nssv536592copy number lossSNP arraySNP genotyping analysisNoHGDP00788GRCh38.p12NC_000001.11133731653384566Remapped1
nstd27nssv536686copy number lossSNP arraySNP genotyping analysisNoHGDP00787GRCh38.p12NC_000001.11136804533755227Remapped1
nstd27nssv536774copy number lossSNP arraySNP genotyping analysisNoHGDP00586GRCh38.p12NC_000001.11139540314020720Remapped1
nstd27nssv536884copy number lossSNP arraySNP genotyping analysisNoHGDP00817GRCh38.p12NC_000001.11140574944239667Remapped1
nstd27nssv536980copy number lossSNP arraySNP genotyping analysisNoHGDP01098GRCh38.p12NC_000001.11145139294532056Remapped1
nstd27nssv537066copy number lossSNP arraySNP genotyping analysisNo1780862093_AGRCh38.p12NC_000001.11146774714693997Remapped1
nstd27nssv537157copy number lossSNP arraySNP genotyping analysisNoNINDS_69GRCh38.p12NC_000001.11121094972158087Remapped1
nstd27nssv537158copy number lossSNP arraySNP genotyping analysisNoNINDS_66GRCh38.p12NC_000001.11146909704727059Remapped1
nstd27nssv537339copy number lossSNP arraySNP genotyping analysisNoHGDP00529GRCh38.p12NC_000001.11150538515113744Remapped1
nstd27nssv537425copy number lossSNP arraySNP genotyping analysisNoHGDP00998GRCh38.p12NC_000001.11152706975288210Remapped1
nstd27nssv537694copy number lossSNP arraySNP genotyping analysisNoHGDP00491GRCh38.p12NC_000001.11160483176124032Remapped1
nstd27nssv537990copy number lossSNP arraySNP genotyping analysisNo1780862021_AGRCh38.p12NC_000001.11163964126512115Remapped1
nstd27nssv538084copy number lossSNP arraySNP genotyping analysisNo1780862101_AGRCh38.p12NC_000001.11121510502251031Remapped1
nstd27nssv538085copy number lossSNP arraySNP genotyping analysisNoNINDS_66GRCh38.p12NC_000001.11164014706504096Remapped1
nstd27nssv538182copy number lossSNP arraySNP genotyping analysisNoNINDS_98GRCh38.p12NC_000001.11164132346504096Remapped1
nstd27nssv538257copy number lossSNP arraySNP genotyping analysisNoHGDP00814GRCh38.p12NC_000001.11164218566508327Remapped1
nstd27nssv538332copy number lossSNP arraySNP genotyping analysisNoHGDP00614GRCh38.p12NC_000001.11164633706520836Remapped1
nstd27nssv538567copy number lossSNP arraySNP genotyping analysisNoHGDP00797GRCh38.p12NC_000001.11171262657171424Remapped1
nstd27nssv538732copy number gainSNP arraySNP genotyping analysisNoHGDP00806GRCh38.p12NC_000001.11189984879020907Remapped1
nstd27nssv538823copy number lossSNP arraySNP genotyping analysisNo1780854205_AGRCh38.p12NC_000001.11190203529072997Remapped1
nstd27nssv538922copy number gainSNP arraySNP genotyping analysisNo1780854392_AGRCh38.p12NC_000001.11192583429327385Remapped1
nstd27nssv539001copy number gainSNP arraySNP genotyping analysisNoHGDP00136GRCh38.p12NC_000001.11192583429336601Remapped1
nstd27nssv539092copy number gainSNP arraySNP genotyping analysisNo1780854556_AGRCh38.p12NC_000001.11192583429336601Remapped1
nstd27nssv539195copy number gainSNP arraySNP genotyping analysisNo1780862577_AGRCh38.p12NC_000001.11192583429352349Remapped1
nstd27nssv539962copy number lossSNP arraySNP genotyping analysisNo1780862414_AGRCh38.p12NC_000001.11122088222263678Remapped1
nstd27nssv539963copy number gainSNP arraySNP genotyping analysisNo1780862066_AGRCh38.p12NC_000001.11192611829336601Remapped1
nstd27nssv540916copy number lossSNP arraySNP genotyping analysisNoHGDP01351GRCh38.p12NC_000001.11122490852289210Remapped1
nstd27nssv541786copy number lossSNP arraySNP genotyping analysisNoHGDP00607GRCh38.p12NC_000001.11124015922496273Remapped1
nstd27nssv542619copy number lossSNP arraySNP genotyping analysisNoHGDP00614GRCh38.p12NC_000001.11124015922518955Remapped1
nstd27nssv632160copy number gain2SNP arraySNP genotyping analysisNoGRCh38.p12NC_000001.11192611829327385Remapped1
nstd27nssv632329copy number loss1SNP arraySNP genotyping analysisNoGRCh38.p12NC_000001.11130098153089567Remapped1
nstd27nssv633422copy number gain1SNP arraySNP genotyping analysisNoGRCh38.p12NC_000001.11150439775110652Remapped1
nstd27nssv633453copy number loss1SNP arraySNP genotyping analysisNoGRCh38.p12NC_000001.11158446585971884Remapped1
nstd27nssv633464copy number loss2SNP arraySNP genotyping analysisNoGRCh38.p12NC_000001.11159473865993570Remapped1
nstd27nssv633486copy number loss2SNP arraySNP genotyping analysisNoGRCh38.p12NC_000001.11160812656144206Remapped1
nstd27nssv633497copy number loss2SNP arraySNP genotyping analysisNoGRCh38.p12NC_000001.11161619156262876Remapped1
nstd27nssv633564copy number loss1SNP arraySNP genotyping analysisNoGRCh38.p12NC_000001.11164903166578004Remapped1
nstd27nssv633575copy number loss2SNP arraySNP genotyping analysisNoGRCh38.p12NC_000001.11165465486630080Remapped1
nstd27nssv633595copy number gain2SNP arraySNP genotyping analysisNoGRCh38.p12NC_000001.11188310669035551Remapped1
nstd27nssv633628copy number loss1SNP arraySNP genotyping analysisNoGRCh38.p12NC_000001.11121821262289210Remapped1
nstd27nssv633672copy number gain1SNP arraySNP genotyping analysisNoGRCh38.p12NC_000001.11192611829327252Remapped1
nstd27nssv633684copy number gain2SNP arraySNP genotyping analysisNoGRCh38.p12NC_000001.11192611829327252Remapped1
nstd27nssv633695copy number gain1SNP arraySNP genotyping analysisNoGRCh38.p12NC_000001.11192611829327385Remapped1
nstd27nssv633706copy number gain2SNP arraySNP genotyping analysisNoGRCh38.p12NC_000001.11192611829327385Remapped1
nstd27nssv633723copy number gain2SNP arraySNP genotyping analysisNoGRCh38.p12NC_000001.11192611829327385Remapped1
nstd27nssv634124copy number loss2SNP arraySNP genotyping analysisNoGRCh38.p12NC_000001.11124591492518955Remapped1
nstd27nsv455661copy number variationNoGRCh38.p12NC_000001.11112172511275912Remapped1
nstd27nsv455662copy number variationNoGRCh38.p12NC_000001.11128529772912986Remapped1
nstd27nsv456773copy number variationNoGRCh38.p12NC_000001.11130098153089567Remapped1
nstd27nsv457884copy number variationNoGRCh38.p12NC_000001.11131457973188066Remapped1
nstd27nsv458995copy number variationNoGRCh38.p12NC_000001.11131671483197116Remapped1
nstd27nsv459950copy number variationNoGRCh38.p12NC_000001.11133731653384566Remapped1
nstd27nsv460061copy number variationNoGRCh38.p12NC_000001.11136804533755227Remapped1
nstd27nsv460172copy number variationNoGRCh38.p12NC_000001.11139540314020720Remapped1
nstd27nsv460283copy number variationNoGRCh38.p12NC_000001.11140574944239667Remapped1
nstd27nsv460394copy number variationNoGRCh38.p12NC_000001.11145139294532056Remapped1
nstd27nsv460505copy number variationNoGRCh38.p12NC_000001.11146774714693997Remapped1
nstd27nsv460616copy number variationNoGRCh38.p12NC_000001.11121094972158087Remapped1
nstd27nsv460617copy number variationNoGRCh38.p12NC_000001.11146909704727059Remapped1
nstd27nsv460728copy number variationNoGRCh38.p12NC_000001.11150439775110652Remapped1
nstd27nsv460839copy number variationNoGRCh38.p12NC_000001.11150538515113744Remapped1
nstd27nsv460950copy number variationNoGRCh38.p12NC_000001.11152706975288210Remapped1
nstd27nsv461061copy number variationNoGRCh38.p12NC_000001.11158446585971884Remapped1
nstd27nsv461172copy number variationNoGRCh38.p12NC_000001.11159473865993570Remapped1
nstd27nsv461283copy number variationNoGRCh38.p12NC_000001.11160483176124032Remapped1
nstd27nsv461394copy number variationNoGRCh38.p12NC_000001.11160812656144206Remapped1
nstd27nsv461505copy number variationNoGRCh38.p12NC_000001.11161619156262876Remapped1
nstd27nsv461616copy number variationNoGRCh38.p12NC_000001.11163964126512115Remapped1
nstd27nsv461727copy number variationNoGRCh38.p12NC_000001.11121510502251031Remapped1
nstd27nsv461728copy number variationNoGRCh38.p12NC_000001.11164014706504096Remapped1
nstd27nsv461839copy number variationNoGRCh38.p12NC_000001.11164132346504096Remapped1
nstd27nsv461950copy number variationNoGRCh38.p12NC_000001.11164218566508327Remapped1
nstd27nsv462061copy number variationNoGRCh38.p12NC_000001.11164633706520836Remapped1
nstd27nsv462172copy number variationNoGRCh38.p12NC_000001.11164903166578004Remapped1
nstd27nsv462283copy number variationNoGRCh38.p12NC_000001.11165465486630080Remapped1
nstd27nsv462394copy number variationNoGRCh38.p12NC_000001.11171262657171424Remapped1
nstd27nsv462505copy number variationNoGRCh38.p12NC_000001.11188310669035551Remapped1
nstd27nsv462616copy number variationNoGRCh38.p12NC_000001.11189984879020907Remapped1
nstd27nsv462727copy number variationNoGRCh38.p12NC_000001.11190203529072997Remapped1
nstd27nsv462838copy number variationNoGRCh38.p12NC_000001.11121821262289210Remapped1
nstd27nsv462839copy number variationNoGRCh38.p12NC_000001.11192583429327385Remapped1
nstd27nsv462950copy number variationNoGRCh38.p12NC_000001.11192583429336601Remapped1
nstd27nsv463061copy number variationNoGRCh38.p12NC_000001.11192583429336601Remapped1
nstd27nsv463172copy number variationNoGRCh38.p12NC_000001.11192583429352349Remapped1
nstd27nsv463283copy number variationNoGRCh38.p12NC_000001.11192611829327252Remapped1
nstd27nsv463394copy number variationNoGRCh38.p12NC_000001.11192611829327252Remapped1
nstd27nsv463505copy number variationNoGRCh38.p12NC_000001.11192611829327385Remapped1
nstd27nsv463616copy number variationNoGRCh38.p12NC_000001.11192611829327385Remapped1
nstd27nsv463727copy number variationNoGRCh38.p12NC_000001.11192611829327385Remapped1
nstd27nsv463838copy number variationNoGRCh38.p12NC_000001.11192611829327385Remapped1
nstd27nsv463949copy number variationNoGRCh38.p12NC_000001.11122088222263678Remapped1
nstd27nsv463950copy number variationNoGRCh38.p12NC_000001.11192611829336601Remapped1
nstd27nsv465060copy number variationNoGRCh38.p12NC_000001.11122490852289210Remapped1
nstd27nsv466171copy number variationNoGRCh38.p12NC_000001.11124015922496273Remapped1
nstd27nsv467282copy number variationNoGRCh38.p12NC_000001.11124015922518955Remapped1
nstd27nsv468393copy number variationNoGRCh38.p12NC_000001.11124591492518955Remapped1
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