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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094169copy number variation1nstd102humanUncertain significance GRCh37 chr11: 46,299,663-46,342,296 , GRCh38.p12 chr11: 46,278,112-46,320,746 CREB3L1
    nsv7060369inversion1nstd229human GRCh38 chr11: 46,320,587-46,320,624 , GRCh37.p13 chr11: 46,342,138-46,342,175 CREB3L1
    nsv6917493copy number variation1nstd229human GRCh38 chr11: 46,297,475-46,297,514 , GRCh37.p13 chr11: 46,319,026-46,319,065 CREB3L1
    nsv6914185copy number variation1nstd229human GRCh38 chr11: 46,313,587-46,318,419 , GRCh37.p13 chr11: 46,335,138-46,339,970 CREB3L1
    nsv6910882copy number variation1nstd229human GRCh38 chr11: 46,298,801-46,303,600 , GRCh37.p13 chr11: 46,320,352-46,325,151 CREB3L1
    nsv6900961copy number variation1nstd229human GRCh38 chr11: 46,299,901-46,317,100 , GRCh37.p13 chr11: 46,321,452-46,338,651 CREB3L1
    nsv6899299copy number variation1nstd229human GRCh38 chr11: 46,317,008-46,319,510 , GRCh37.p13 chr11: 46,338,559-46,341,061 CREB3L1
    nsv6583715inversion1nstd223human GRCh38 chr11: 46,282,413-46,283,476 , GRCh37.p13 chr11: 46,303,964-46,305,027 CREB3L1
    nsv6471632copy number variation1nstd223human GRCh38 chr11: 46,319,678-46,326,170 , GRCh37.p13 chr11: 46,341,229-46,347,720 CREB3L1
    nsv6468173copy number variation1nstd223human GRCh38 chr11: 46,317,804-46,319,799 , GRCh37.p13 chr11: 46,339,355-46,341,350 CREB3L1
    nsv6466580copy number variation1nstd223human GRCh38 chr11: 46,277,601-46,278,200 , GRCh37.p13 chr11: 46,299,152-46,299,751 CREB3L1
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6313964copy number variation1nstd102humanUncertain significance GRCh37 chr11: 46,248,477-46,748,132 , GRCh38.p12 chr11: 46,226,926-46,726,582 ARHGAP1, F2, 13 more genes
    nsv6309197copy number variation1nstd102humanUncertain significance GRCh37 chr11: 46,318,032-46,761,066 , GRCh38.p12 chr11: 46,296,481-46,739,516 MIR3160-2, RPS10P19, 12 more genes
    nsv6309196copy number variation1nstd102humanPathogenic GRCh37 chr11: 45,827,353-46,401,497 , GRCh38.p12 chr11: 45,805,802-46,379,947 LINC02710, PHF21A, 14 more genes
    nsv6308565insertion1nstd186human GRCh37 chr11: 46,303,963-46,303,963 , GRCh38.p12 chr11: 46,282,412-46,282,412 CREB3L1
    nsv6293918mobile element insertion1nstd186human GRCh37 chr11: 46,318,026-46,318,077 , GRCh38.p12 chr11: 46,296,475-46,296,526 CREB3L1
    nsv6291196copy number variation1nstd102humanPathogenic GRCh37 chr11: 40,117,145-46,920,718 , GRCh38.p12 chr11: 40,095,595-46,899,167 LINC02687, ALKBH3, 86 more genes
    nsv6206664copy number variation1nstd214human GRCh38 chr11: 46,313,160-46,313,251 , GRCh37.p13 chr11: 46,334,711-46,334,802 CREB3L1
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