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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5953645insertion1nstd209human GRCh38 chr6: 26,187,715-26,187,715 , GRCh37.p13 chr6: 26,187,943-26,187,943 H4C4
    nsv5688907mobile element insertion2nstd211human GRCh38 chr6: 26,187,723-26,187,723 , GRCh37.p13 chr6: 26,187,951-26,187,951 H4C4
    nsv5631209insertion1nstd207human GRCh38 chr6: 26,187,715-26,187,715 , GRCh37.p13 chr6: 26,187,943-26,187,943 H4C4
    nsv5540062insertion1nstd206human GRCh38 chr6: 26,187,723-26,187,766 , GRCh37.p13 chr6: 26,187,951-26,187,994 H4C4
    nsv5227740copy number variation1nstd204human GRCh38.p13 chr6: 26,178,386-26,196,804 , GRCh37.p13 chr6: 26,178,614-26,197,032 H2BC6, H3C4, 3 more genes
    nsv5119569mobile element insertion1nstd203human GRCh38 chr6: 26,187,714-26,187,723 , GRCh37.p13 chr6: 26,187,942-26,187,951 H4C4
    nsv5118935mobile element insertion1nstd203human GRCh38 chr6: 26,187,713-26,187,723 , GRCh37.p13 chr6: 26,187,941-26,187,951 H4C4
    nsv5106926mobile element insertion1nstd203human GRCh38 chr6: 26,187,715-26,187,723 , GRCh37.p13 chr6: 26,187,943-26,187,951 H4C4
    nsv5106426mobile element insertion1nstd203human GRCh38 chr6: 26,187,984-26,187,999 , GRCh37.p13 chr6: 26,188,212-26,188,227 H4C4
    nsv5104777mobile element insertion1nstd203human GRCh38 chr6: 26,187,723-26,187,723 , GRCh37.p13 chr6: 26,187,951-26,187,951 H4C4
    nsv5100097mobile element insertion1nstd203human GRCh38 chr6: 26,187,720-26,187,723 , GRCh37.p13 chr6: 26,187,948-26,187,951 H4C4
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4934536copy number variation1nstd200human GRCh38 chr6: 26,150,781-26,331,570 , GRCh37.p13 chr6: 26,151,009-26,331,798 , LARP1P1, 41 more genes
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 more genes
    nsv4762977insertion1nstd199human GRCh37 chr6: 26,187,949-26,187,949 , GRCh38.p12 chr6: 26,187,721-26,187,721 H4C4
    nsv4729341copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,046,566-26,670,193 , GRCh38.p12 chr6: 26,046,338-26,669,965 H1-4, TRV-CAC1-6, 78 more genes
    nsv4728787copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,090,243-26,265,667 , GRCh38.p12 chr6: 26,090,015-26,265,439 H2AC7, H2AC9P, 26 more genes
    nsv4720933insertion1nstd186human GRCh37 chr6: 26,187,943-26,187,943 , GRCh38.p12 chr6: 26,187,715-26,187,715 H4C4
    nsv4692440mobile element insertion1nstd186human GRCh37 chr6: 26,187,951-26,187,951 , GRCh38.p12 chr6: 26,187,723-26,187,723 H4C4
    nsv4598439copy number variation1nstd183human GRCh37 chr6: 26,153,284-26,235,966 , GRCh38.p12 chr6: 26,153,056-26,235,738 H1-3, H2BC7, 15 more genes
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