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Items: 1 to 20 of 223

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094186copy number variation1nstd102humanUncertain significance GRCh37 chr11: 721,044-3,988,932 , GRCh38.p12 chr11: 721,044-3,967,702 OR7E117P, RPLP2, 124 more genes
    nsv7093761copy number variation1nstd102humanUncertain significance GRCh37 chr11: 1,278,740-2,906,719 , GRCh38.p12 chr11: 1,257,510-2,885,489 TOLLIP-DT, KRTAP5-6, 58 more genes
    nsv7061927inversion1nstd229human GRCh38 chr11: 1,707,646-1,896,713 , GRCh37.p13 chr11: 1,728,876-1,917,943 MIR4298, LOC390029, 10 more genes
    nsv6917727copy number variation1nstd229human GRCh38 chr11: 1,745,501-1,746,500 , GRCh37.p13 chr11: 1,766,731-1,767,730 IFITM10
    nsv6916868copy number variation1nstd229human GRCh38 chr11: 1,744,968-1,748,032 , GRCh37.p13 chr11: 1,766,198-1,769,262 IFITM10
    nsv6915480copy number variation1nstd229human GRCh38 chr11: 1,735,811-1,821,007 , GRCh37.p13 chr11: 1,757,041-1,842,237 CTSD, IFITM10, 3 more genes
    nsv6907605copy number variation1nstd229human GRCh38 chr11: 1,743,687-1,747,695 , GRCh37.p13 chr11: 1,764,917-1,768,925 IFITM10
    nsv6902302copy number variation1nstd229human GRCh38 chr11: 1,733,301-1,744,600 , GRCh37.p13 chr11: 1,754,531-1,765,830 IFITM10
    nsv6901271copy number variation1nstd229human GRCh38 chr11: 1,733,223-1,744,642 , GRCh37.p13 chr11: 1,754,453-1,765,872 IFITM10
    nsv6888081copy number variation1nstd229human GRCh38 chr11: 1,727,950-1,781,336 , GRCh37.p13 chr11: 1,749,180-1,802,566 CTSD, LOC105376517, 1 more genes
    nsv6885276copy number variation1nstd229human GRCh38 chr11: 1,136,035-3,145,463 , GRCh37.p13 chr11: 1,129,943-3,166,693 KRTAP5-1, MIR675, 69 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
    nsv6637212copy number variation1nstd102humanPathogenic GRCh37 chr11: 461,373-2,157,956 , GRCh38.p12 chr11: 461,373-2,136,726 MIR6744, PTDSS2, 80 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
    nsv6620716copy number variation1nstd224human GRCh37 chr11: 1,769,085-1,849,354 , GRCh38.p12 chr11: 1,747,855-1,828,124 CTSD, SYT8, 4 more genes
    nsv6620713copy number variation1nstd224human GRCh37 chr11: 1,629,693-1,881,256 , GRCh38.p12 chr11: 1,608,463-1,860,026 , GRCh38.p12 chr11|NT_187657.1: 85,016-214,625 TNNI2, KRTAP5-3, 15 more genes
    nsv6455025copy number variation1nstd223human GRCh38 chr11: 1,745,868-1,745,971 , GRCh37.p13 chr11: 1,767,098-1,767,201 IFITM10
    nsv6443668copy number variation1nstd223human GRCh38 chr11: 1,733,223-1,744,643 , GRCh37.p13 chr11: 1,754,453-1,765,873 IFITM10
    nsv6440752copy number variation1nstd223human GRCh38 chr11: 1,730,934-1,731,221 , GRCh37.p13 chr11: 1,752,164-1,752,451 IFITM10
    nsv6438165copy number variation1nstd223human GRCh38 chr11: 737,066-3,896,161 , GRCh37.p13 chr11: 737,066-3,917,391 RNU6-878P, CARS1-AS1, 123 more genes
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