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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5596813copy number variation1nstd207human GRCh38 chr14: 89,288,692-89,288,743 , GRCh37.p13 chr14: 89,755,036-89,755,087 CAP2P1, FOXN3
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5142965mobile element insertion1nstd203human GRCh38 chr14: 89,289,850-89,289,862 , GRCh37.p13 chr14: 89,756,194-89,756,206 CAP2P1, FOXN3
    nsv4748998copy number variation1nstd199human GRCh37 chr14: 89,754,996-89,755,077 , GRCh38.p12 chr14: 89,288,652-89,288,733 CAP2P1, FOXN3
    nsv4675107copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,783,523-96,907,490 , GRCh38.p12 chr14: 84,317,179-96,441,153 SHLD2P2, RPL15P2, 175 more genes
    nsv4516349mobile element insertion1nstd166human GRCh37.p13 chr14: 89,756,194-89,756,194 , GRCh38.p12 chr14: 89,289,850-89,289,850 FOXN3, CAP2P1
    nsv4456664copy number variation1nstd102humanPathogenic GRCh37 chr14: 77,274,990-89,803,137 , GRCh38.p12 chr14: 76,808,647-89,336,793 DYNLL1P2, GTF2A1, 126 more genes
    nsv4220089copy number variation1nstd166human GRCh37.p13 chr14: 89,754,279-89,755,094 , GRCh38.p12 chr14: 89,287,935-89,288,750 CAP2P1, FOXN3
    nsv4216181copy number variation1nstd166human GRCh37.p13 chr14: 89,757,309-89,757,498 , GRCh38.p12 chr14: 89,290,965-89,291,154 FOXN3, CAP2P1
    nsv3922094copy number variation1nstd102humanPathogenic GRCh38 chr14: 73,655,772-106,879,298 , GRCh37 chr14: 74,122,475-107,287,505 , NCBI36 chr14: 73,192,228-106,358,550 LOC105370614, LOC105370617, 849 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
    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
    nsv3915681copy number variation1nstd102humanPathogenic NCBI36 chr14: 76,758,891-106,358,550 , GRCh37 chr14: 77,689,138-107,287,505 , GRCh38 chr14: 77,222,795-106,879,298 IGHV3-32, SNORD114-31, 751 more genes
    nsv3914983copy number variation1nstd102humanPathogenic GRCh38 chr14: 86,094,030-106,832,642 , GRCh37 chr14: 86,560,374-107,240,869 , NCBI36 chr14: 85,630,127-106,311,914 IGHD5-5, EML5, 658 more genes
    nsv3913338copy number variation1nstd102humanUncertain significance NCBI36 chr14: 88,815,579-89,245,151 , GRCh37 chr14: 89,745,826-90,175,398 , GRCh38 chr14: 89,279,482-89,709,054 CAP2P1, LOC105370616, 7 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
    nsv3906086copy number variation1nstd102humanUncertain significance GRCh37 chr14: 89,586,296-89,904,864 , GRCh38.p12 chr14: 89,119,952-89,438,520 FOXN3, LOC107984635, 3 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
    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
    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
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