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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6913212copy number variation1nstd229human GRCh38 chr11: 5,742,188-5,844,344 , GRCh37.p13 chr11: 5,763,418-5,865,574 OR56B2P, OR52N3P, 5 more genes
    nsv6911925copy number variation1nstd229human GRCh38 chr11: 5,840,801-5,852,000 , GRCh37.p13 chr11: 5,862,031-5,873,230 OR52E6
    nsv6910451copy number variation1nstd229human GRCh38 chr11: 5,839,550-5,848,539 , GRCh37.p13 chr11: 5,860,780-5,869,769 OR52E6
    nsv6902633copy number variation1nstd229human GRCh38 chr11: 5,538,086-5,938,396 , GRCh37.p13 chr11: 5,559,316-5,959,626 OR52N1, OR52N4, 26 more genes
    nsv6899903copy number variation1nstd229human GRCh38 chr11: 5,838,281-5,849,660 , GRCh37.p13 chr11: 5,859,511-5,870,890 OR52E6
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6621251copy number variation1nstd224human GRCh37 chr11: 5,727,822-5,995,159 , GRCh38.p12 chr11: 5,706,592-5,973,929 TRIM22, OR52N1, 17 more genes
    nsv6590262inversion1nstd223human GRCh38 chr11: 5,786,169-5,868,284 , GRCh37.p13 chr11: 5,807,399-5,889,514 OR52N1, OR52N3P, 3 more genes
    nsv6453358copy number variation1nstd223human GRCh38 chr11: 5,836,307-5,844,321 , GRCh37.p13 chr11: 5,857,537-5,865,551 OR52E6
    nsv6442366copy number variation1nstd223human GRCh38 chr11: 5,838,281-5,849,659 , GRCh37.p13 chr11: 5,859,511-5,870,889 OR52E6
    nsv6441849copy number variation1nstd223human GRCh38 chr11: 5,588,812-6,011,442 , GRCh37.p13 chr11: 5,610,042-6,032,672 OR52N5, OR52N4, 26 more genes
    nsv6437487copy number variation1nstd223human GRCh38 chr11: 5,568,264-6,075,481 , GRCh37.p13 chr11: 5,589,494-6,096,711 TRIM34, OR52E6, 33 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv5373406translocation1nstd200human GRCh38 chr11: 5,844,187-5,844,187 , GRCh38 chr11: 5,839,790-5,839,790 , GRCh37.p13 chr11: 5,861,020-5,861,020 , GRCh37.p13 chr11: 5,865,417-5,865,417 OR52E6
    nsv5373405translocation1nstd200human GRCh38 chr11: 5,839,673-5,839,673 , GRCh38 chr11: 5,849,530-5,849,530 , GRCh37.p13 chr11: 5,860,903-5,860,903 , GRCh37.p13 chr11: 5,870,760-5,870,760 OR52E6
    nsv4978025copy number variation1nstd200human GRCh38 chr11: 5,836,307-5,844,321 , GRCh37.p13 chr11: 5,857,537-5,865,551 OR52E6
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    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
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