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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5507991copy number variation1nstd206human GRCh38 chr14: 103,182,518-103,185,320 , GRCh37.p13 chr14: 103,648,855-103,651,657 LINC00605, GCSHP2
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5357630translocation1nstd200human GRCh38 chr14: 103,185,320-103,185,320 , GRCh38 chr14: 103,182,518-103,182,518 , GRCh37.p13 chr14: 103,648,855-103,648,855 , GRCh37.p13 chr14: 103,651,657-103,651,657 LINC00605, GCSHP2
    nsv5279907copy number variation1nstd204human GRCh38.p13 chr14: 103,184,243-103,190,287 , GRCh37.p13 chr14: 103,650,580-103,656,624 LINC00605, GCSHP2
    nsv5005025copy number variation1nstd200human GRCh38 chr14: 103,065,408-103,252,792 , GRCh37.p13 chr14: 103,531,745-103,719,129 RPL21P13, NDUFB4P11, 8 more genes
    nsv4991496copy number variation1nstd200human GRCh38 chr14: 103,187,605-103,197,893 , GRCh37.p13 chr14: 103,653,942-103,664,230 LINC00605
    nsv4855069copy number variation1nstd200human GRCh37 chr14: 103,653,942-103,664,230 , GRCh38.p12 chr14: 103,187,605-103,197,893 LINC00605
    nsv4855068copy number variation1nstd200human GRCh37 chr14: 103,648,855-103,651,657 , GRCh38.p12 chr14: 103,182,518-103,185,320 LINC00605, GCSHP2
    nsv4855067copy number variation1nstd200human GRCh37 chr14: 103,643,059-103,654,760 , GRCh38.p12 chr14: 103,176,722-103,188,423 GCSHP2, LINC00605
    nsv4729218copy number variation1nstd102humanPathogenic GRCh37 chr14: 102,615,953-107,285,437 , GRCh38.p12 chr14: 102,149,616-106,877,229 IGHV4-61, IGHD3-9, 308 more genes
    nsv4684265copy number variation1nstd102humanPathogenic GRCh37 chr14: 96,829,290-107,287,663 , GRCh38.p12 chr14: 96,362,953-106,879,456 NDUFB3P4, LINC02320, 502 more genes
    nsv4669559copy number variation1nstd186human GRCh37 chr14: 103,648,835-103,651,642 , GRCh38.p12 chr14: 103,182,498-103,185,305 LINC00605, GCSHP2
    nsv4633282copy number variation1nstd183human GRCh37 chr14: 103,641,997-103,722,462 , GRCh38.p12 chr14: 103,175,660-103,256,125 RPL21P13, LOC105370685, 2 more genes
    nsv4619115copy number variation1nstd183human GRCh37 chr14: 103,648,835-103,651,642 , GRCh38.p12 chr14: 103,182,498-103,185,305 GCSHP2, LINC00605
    nsv4456944copy number variation1nstd102humanPathogenic GRCh37 chr14: 101,627,916-107,147,698 , GRCh38.p12 chr14: 101,161,579-106,691,681 IGHV1-58, IGHVII-60-1, 308 more genes
    nsv4456320copy number variation1nstd102humanPathogenic GRCh37 chr14: 102,931,119-107,285,437 , GRCh38.p12 chr14: 102,464,782-106,877,229 LOC105378184, LINC02298, 302 more genes
    nsv4456178copy number variation1nstd102humanPathogenic GRCh37 chr14: 91,969,028-107,285,437 , GRCh38.p12 chr14: 91,502,684-106,877,229 LOC105370639, SERPINA9, 600 more genes
    nsv4455156copy number variation1nstd102humanPathogenic GRCh37 chr14: 99,794,230-107,285,437 , GRCh38.p12 chr14: 99,327,893-106,877,229 IGHG4, IGHV3-57, 464 more genes
    nsv4416653copy number variation1nstd174human GRCh37 chr14: 103,648,739-103,651,789 , GRCh38.p12 chr14: 103,182,402-103,185,452 LINC00605, GCSHP2
    nsv4349480copy number variation1nstd102humanPathogenic GRCh37 chr14: 100,575,917-107,281,934 , GRCh38.p12 chr14: 100,109,580-106,873,725 IGHD2-21, MIR300, 452 more genes
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