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Items: 1 to 20 of 145

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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
    nsv6915763copy number variation1nstd229human GRCh38 chr11: 4,804,075-4,843,746 , GRCh37.p13 chr11: 4,825,305-4,864,976 OR51F2, OR51A8P, 1 more genes
    nsv6903296copy number variation1nstd229human GRCh38 chr11: 4,779,903-4,889,353 , GRCh37.p13 chr11: 4,801,133-4,910,583 OR52Y1P, OR51F2, 8 more genes
    nsv6903025copy number variation1nstd229human GRCh38 chr11: 4,682,156-5,202,827 , GRCh37.p13 chr11: 4,703,386-5,224,057 OR51V1, OR51L1, 39 more genes
    nsv6902995copy number variation1nstd229human GRCh38 chr11: 4,619,101-5,268,938 , GRCh37.p13 chr11: 4,640,331-5,290,168 OR51A9P, OR51F1, 50 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
    nsv6634327copy number variation1nstd102humanPathogenic GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927 SNORA54, PIDD1, 219 more genes
    nsv6621235copy number variation1nstd224human GRCh37 chr11: 4,811,083-4,909,000 , GRCh38.p12 chr11: 4,789,853-4,887,770 OR52Y1P, OR51S1, 7 more genes
    nsv6621234copy number variation1nstd224human GRCh37 chr11: 4,806,282-4,870,266 , GRCh38.p12 chr11: 4,785,052-4,849,036 OR52Y1P, OR51S1, 4 more genes
    nsv6450577copy number variation1nstd223human GRCh38 chr11: 4,619,075-5,268,953 , GRCh37.p13 chr11: 4,640,305-5,290,183 OR52J1P, OR51F2, 50 more genes
    nsv6443009copy number variation1nstd223human GRCh38 chr11: 4,779,903-4,889,350 , GRCh37.p13 chr11: 4,801,133-4,910,580 OR51H2P, OR51F2, 8 more genes
    nsv6439692copy number variation1nstd223human GRCh38 chr11: 4,682,156-5,202,827 , GRCh37.p13 chr11: 4,703,386-5,224,057 OR51S1, OR51F1, 39 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
    nsv6291427copy number variation1nstd102humannot provided GRCh37 chr11: 230,615-5,525,355 , GRCh38.p12 chr11: 230,615-5,504,125 OR52J1P, IFITM1, 255 more genes
    nsv6291414copy number variation1nstd102humanLikely benign GRCh37 chr11: 4,781,648-4,899,547 , GRCh38.p12 chr11: 4,760,418-4,878,317 OR52Y1P, OR51S1, 7 more genes
    nsv6132106copy number variation1nstd213human GRCh37 chr11: 4,510,000-5,300,001 , GRCh38.p12 chr11: 4,488,770-5,278,771 HBB, HBBP1, 57 more genes
    nsv5500962copy number variation1nstd206human GRCh38 chr11: 4,779,903-4,889,350 , GRCh37.p13 chr11: 4,801,133-4,910,580 OR51T1, OR51H1, 8 more genes
    nsv4984159copy number variation1nstd200human GRCh38 chr11: 4,778,528-4,801,920 , GRCh37.p13 chr11: 4,799,758-4,823,150 OR52Y1P, OR51N1P, 1 more genes
    nsv4977973copy number variation1nstd200human GRCh38 chr11: 4,779,903-4,889,350 , GRCh37.p13 chr11: 4,801,133-4,910,580 OR51A6P, OR51S1, 8 more genes
    nsv4977972copy number variation1nstd200human GRCh38 chr11: 4,764,800-4,880,524 , GRCh37.p13 chr11: 4,786,030-4,901,754 OR51H1, OR52Y1P, 8 more genes
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