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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5944951copy number variation1nstd209human GRCh38 chr15: 88,646,389-88,660,731 , GRCh37.p13 chr15: 89,189,620-89,203,962 ISG20
    nsv5887032copy number variation1nstd209human GRCh38 chr15: 88,652,594-88,660,431 , GRCh37.p13 chr15: 89,195,825-89,203,662 ISG20
    nsv5868981copy number variation1nstd209human GRCh38 chr15: 88,646,005-88,653,393 , GRCh37.p13 chr15: 89,189,236-89,196,624 ISG20
    nsv5598572copy number variation1nstd207human GRCh38 chr15: 88,652,389-88,652,449 , GRCh37.p13 chr15: 89,195,620-89,195,680 ISG20
    nsv5532726copy number variation1nstd206human GRCh38 chr15: 88,646,358-88,646,458 , GRCh37.p13 chr15: 89,189,589-89,189,689 ISG20
    nsv5515905copy number variation1nstd206human GRCh38 chr15: 88,635,723-88,635,791 , GRCh37.p13 chr15: 89,178,954-89,179,022 ISG20
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5276511copy number variation1nstd204human GRCh38.p13 chr15: 88,637,401-88,646,600 , GRCh37.p13 chr15: 89,180,632-89,189,831 ISG20
    nsv5196068mobile element insertion1nstd203human GRCh38 chr15: 88,637,361-88,637,376 , GRCh37.p13 chr15: 89,180,592-89,180,607 ISG20
    nsv5009146copy number variation1nstd200human GRCh38 chr15: 88,638,327-88,690,831 , GRCh37.p13 chr15: 89,181,558-89,234,062 ISG20
    nsv5009145copy number variation1nstd200human GRCh38 chr15: 88,625,152-88,641,502 , GRCh37.p13 chr15: 89,168,383-89,184,733 AEN, ISG20
    nsv5002258copy number variation1nstd200human GRCh38 chr15: 88,640,295-88,646,229 , GRCh37.p13 chr15: 89,183,526-89,189,460 ISG20
    nsv4863944copy number variation1nstd200human GRCh37 chr15: 89,189,620-89,203,963 , GRCh38.p12 chr15: 88,646,389-88,660,732 ISG20
    nsv4856235copy number variation1nstd200human GRCh37 chr15: 89,183,526-89,189,460 , GRCh38.p12 chr15: 88,640,295-88,646,229 ISG20
    nsv4747315copy number variation1nstd199human GRCh37 chr15: 89,195,613-89,195,682 , GRCh38.p12 chr15: 88,652,382-88,652,451 ISG20
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
    nsv4625274copy number variation1nstd183human GRCh37 chr15: 89,169,494-89,183,054 , GRCh38.p12 chr15: 88,626,263-88,639,823 ISG20, AEN
    nsv4447591copy number variation1nstd175human GRCh37 chr15: 89,195,551-89,195,654 , GRCh38.p12 chr15: 88,652,320-88,652,423 ISG20
    nsv4428905copy number variation1nstd174human GRCh37 chr15: 89,179,676-89,198,900 , GRCh38.p12 chr15: 88,636,445-88,655,669 ISG20
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