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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137096copy number variation1nstd102humanLikely benign GRCh37 chr11: 5,094,756-5,785,959 , GRCh38.p12 chr11: 5,073,526-5,764,729 OR51J1, OLFM5P, 52 more genes
    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
    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
    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
    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
    nsv6440985copy number variation1nstd223human GRCh38 chr11: 5,727,317-5,728,426 , GRCh37.p13 chr11: 5,748,547-5,749,656 OR52P1, OR52N4
    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
    nsv6436757copy number variation1nstd223human GRCh38 chr11: 5,618,722-5,835,186 , GRCh37.p13 chr11: 5,639,952-5,856,416 OR56B2P, OR52P1, 12 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
    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
    nsv4729727copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,642,000-5,853,662 , GRCh38.p12 chr11: 5,620,770-5,832,432 OR52N3P, OR56B1, 12 more genes
    nsv4681173copy number variation2nstd102humanUncertain significance GRCh37 chr11: 5,709,028-6,640,651 , GRCh38.p12 chr11: 5,687,798-6,619,420 OR56B2P, TRIM3, 50 more genes
    nsv4675693copy number variation1nstd102humanLikely benign GRCh37 chr11: 5,505,304-6,199,376 , GRCh38.p12 chr11: 5,484,074-6,178,146 OR52B5P, HNRNPA1P53, 47 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
    nsv4387795copy number variation1nstd173human GRCh37 chr11: 5,067,391-6,257,231 , GRCh38.p12 chr11: 5,046,161-6,236,001 HBD, OR52N2, 85 more genes
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv3955490copy number variation1nstd168human GRCh38 chr11: 5,709,294-5,873,254 , GRCh37.p13 chr11: 5,730,524-5,894,484 OR52P1, OR52E7P, 11 more genes
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