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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5916663copy number variation1nstd209human GRCh38 chr11: 8,818,116-8,977,319 , GRCh37.p13 chr11: 8,839,663-8,998,866 DENND2B, AKIP1, 5 more genes
    nsv5914018copy number variation1nstd209human GRCh38 chr11: 8,936,470-8,943,580 , GRCh37.p13 chr11: 8,958,017-8,965,127 ASCL3
    nsv5860399copy number variation1nstd209human GRCh38 chr11: 8,936,465-8,942,729 , GRCh37.p13 chr11: 8,958,012-8,964,276 ASCL3
    nsv5652640insertion1nstd207human GRCh38 chr11: 8,936,601-8,936,601 , GRCh37.p13 chr11: 8,958,148-8,958,148 ASCL3
    nsv5499829copy number variation1nstd206human GRCh38 chr11: 8,936,502-8,943,581 , GRCh37.p13 chr11: 8,958,049-8,965,128 ASCL3
    nsv5498315copy number variation1nstd206human GRCh38 chr11: 8,934,322-8,936,079 , GRCh37.p13 chr11: 8,955,869-8,957,626 ASCL3
    nsv5342642translocation1nstd200human GRCh37 chr11: 8,965,128-8,965,128 , GRCh37 chr11: 8,958,049-8,958,049 , GRCh38.p12 chr11: 8,943,581-8,943,581 , GRCh38.p12 chr11: 8,936,502-8,936,502 ASCL3
    nsv5313304copy number variation1nstd204human GRCh38.p13 chr11: 8,936,472-8,943,602 , GRCh37.p13 chr11: 8,958,019-8,965,149 ASCL3
    nsv5254339copy number variation1nstd204human GRCh38.p13 chr11: 8,936,501-8,943,200 , GRCh37.p13 chr11: 8,958,048-8,964,747 ASCL3
    nsv5243586copy number variation1nstd204human GRCh38.p13 chr11: 8,936,440-8,943,129 , GRCh37.p13 chr11: 8,957,987-8,964,676 ASCL3
    nsv5138406mobile element insertion1nstd203human GRCh38 chr11: 8,936,617-8,936,653 , GRCh37.p13 chr11: 8,958,164-8,958,200 ASCL3
    nsv5127022mobile element insertion1nstd203human GRCh38 chr11: 8,936,623-8,936,653 , GRCh37.p13 chr11: 8,958,170-8,958,200 ASCL3
    nsv4978152copy number variation1nstd200human GRCh38 chr11: 8,936,502-8,943,581 , GRCh37.p13 chr11: 8,958,049-8,965,128 ASCL3
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4675904copy number variation1nstd102humanUncertain significance GRCh37 chr11: 8,859,352-9,226,956 , GRCh38.p12 chr11: 8,837,805-9,205,409 DENND2B, TMEM9B-AS1, 12 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4612103copy number variation1nstd183human GRCh37 chr11: 8,958,719-8,964,824 , GRCh38.p12 chr11: 8,937,172-8,943,277 ASCL3
    nsv4610580copy number variation1nstd183human GRCh37 chr11: 8,958,065-8,965,176 , GRCh38.p12 chr11: 8,936,518-8,943,629 ASCL3
    nsv4599816copy number variation1nstd183human GRCh37 chr11: 8,950,080-8,974,773 , GRCh38.p12 chr11: 8,928,533-8,953,226 C11orf16, ASCL3, 1 more genes
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