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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1746374short tandem repeat2nstd128human GRCh37 chr14: 64,060,546-64,060,568 , GRCh38.p12 chr14: 63,593,828-63,593,850 GCATP1
    nsv1746130short tandem repeat2nstd128human GRCh37 chr14: 64,060,480-64,060,492 , GRCh38.p12 chr14: 63,593,762-63,593,774 GCATP1
    nsv5495499copy number variation1nstd206human GRCh38 chr14: 63,589,727-63,596,394 , GRCh37.p13 chr14: 64,056,445-64,063,112 GCATP1, WDR89
    esv3873262copy number variation2estd219human GRCh37 chr14: 64,056,332-64,063,105 , GRCh38.p12 chr14: 63,589,614-63,596,387 WDR89, GCATP1
    esv3634733copy number variation2estd214human GRCh37 chr14: 64,056,332-64,063,105 , GRCh38.p12 chr14: 63,589,614-63,596,387 GCATP1, WDR89
    nsv5269977copy number variation1nstd204human GRCh38.p13 chr14: 63,590,598-63,596,072 , GRCh37.p13 chr14: 64,057,316-64,062,790 WDR89, GCATP1
    esv3873263copy number variation1estd219human GRCh37 chr14: 64,056,822-64,086,427 , GRCh38.p12 chr14: 63,590,104-63,619,709 WDR89, GCATP1, 2 more genes
    esv3634734copy number variation1estd214human GRCh37 chr14: 64,056,822-64,086,427 , GRCh38.p12 chr14: 63,590,104-63,619,709 HSPE1P2, RNU6-597P, 2 more genes
    nsv3922652copy number variation1nstd102humanPathogenic GRCh37 chr14: 57,507,754-67,674,948 , NCBI36 chr14: 56,577,507-66,744,701 , GRCh38 chr14: 57,041,036-67,208,231 PARP1P2, SNAPC1, 160 more genes
    nsv3923965copy number variation1nstd102humanPathogenic GRCh37 chr14: 60,383,769-67,217,521 , NCBI36 chr14: 59,453,522-66,287,274 , GRCh38 chr14: 59,917,051-66,750,803 ESR2, PPP2R5E, 111 more genes
    nsv3924033copy number variation1nstd102humanPathogenic GRCh37 chr14: 58,120,131-64,560,246 , GRCh38 chr14: 57,653,413-64,093,528 , NCBI36 chr14: 57,189,884-63,629,999 DACT1, UBA52P3, 105 more genes
    nsv3912530copy number variation1nstd102humanPathogenic NCBI36 chr14: 61,789,171-65,289,887 , GRCh38 chr14: 62,252,700-65,753,416 , GRCh37 chr14: 62,719,418-66,220,134 MIR625, LINC02324, 59 more genes
    nsv3902883copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863 LOC440181, HEATR5A-DT, 1998 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 BANF1P1, IGHV1-68, 1996 more genes
    nsv3899639copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456 LOC100289511, RNU6-552P, 1996 more genes
    nsv3903256copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050 DHRS7, MIR548Y, 1946 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 SRMP2, IGHV3-71, 1929 more genes
    nsv3904265copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229 CRIP1, GPATCH2L, 1929 more genes
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 MIR656, TRAJ59, 1918 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
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