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Items: 1 to 20 of 270

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146752copy number variation1nstd232human GRCh37.p13 chr11: 2,329,699-2,329,829 , GRCh38.p12 chr11: 2,308,469-2,308,599 TSPAN32
    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
    nsv6917613copy number variation1nstd229human GRCh38 chr11: 2,300,701-2,308,400 , GRCh37.p13 chr11: 2,321,931-2,329,630 TSPAN32, C11orf21
    nsv6915830copy number variation1nstd229human GRCh38 chr11: 2,300,347-2,305,418 , GRCh37.p13 chr11: 2,321,577-2,326,648 TSPAN32, C11orf21
    nsv6907816copy number variation1nstd229human GRCh38 chr11: 2,302,022-2,317,107 , GRCh37.p13 chr11: 2,323,252-2,338,337 C11orf21, TSPAN32
    nsv6906116copy number variation1nstd229human GRCh38 chr11: 2,211,996-2,356,501 , GRCh37.p13 chr11: 2,233,226-2,377,731 C11orf21, RPL26P30, 4 more genes
    nsv6902434copy number variation1nstd229human GRCh38 chr11: 2,305,622-2,319,307 , GRCh37.p13 chr11: 2,326,852-2,340,537 TSPAN32
    nsv6901605copy number variation1nstd229human GRCh38 chr11: 2,257,028-2,326,666 , GRCh37.p13 chr11: 2,278,258-2,347,896 C11orf21, ASCL2, 2 more genes
    nsv6898831copy number variation1nstd229human GRCh38 chr11: 2,300,061-2,330,106 , GRCh37.p13 chr11: 2,321,291-2,351,336 TSPAN32, CD81-AS1, 2 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
    nsv6634327copy number variation1nstd102humanPathogenic GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927 SNORA54, PIDD1, 219 more genes
    nsv6441697copy number variation1nstd223human GRCh38 chr11: 2,278,982-2,299,438 , GRCh37.p13 chr11: 2,300,212-2,320,668 TSPAN32, C11orf21
    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
    nsv6437128copy number variation1nstd223human GRCh38 chr11: 2,212,082-2,356,488 , GRCh37.p13 chr11: 2,233,312-2,377,718 ASCL2, CD81-AS1, 4 more genes
    nsv6315544copy number variation1nstd102humanUncertain significance GRCh37 chr11: 2,314,240-2,915,570 , GRCh38.p12 chr11: 2,293,010-2,894,340 COX6CP18, SLC22A18AS, 14 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
    nsv6303570copy number variation1nstd186human GRCh37 chr11: 2,321,315-2,351,336 , GRCh38.p12 chr11: 2,300,085-2,330,106 TSPAN32, C11orf21, 2 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
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