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Items: 1 to 20 of 292

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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
    nsv6910708copy number variation1nstd229human GRCh38 chr11: 2,411,401-2,417,700 , GRCh37.p13 chr11: 2,432,631-2,438,930 TRPM5
    nsv6910097copy number variation1nstd229human GRCh38 chr11: 2,404,701-2,410,200 , GRCh37.p13 chr11: 2,425,931-2,431,430 TRPM5
    nsv6907380copy number variation1nstd229human GRCh38 chr11: 2,422,167-2,425,320 , GRCh37.p13 chr11: 2,443,397-2,446,550 TRPM5
    nsv6906429copy number variation1nstd229human GRCh38 chr11: 2,415,501-2,420,300 , GRCh37.p13 chr11: 2,436,731-2,441,530 TRPM5
    nsv6899345copy number variation1nstd229human GRCh38 chr11: 2,386,473-2,487,577 , GRCh37.p13 chr11: 2,407,703-2,508,807 KCNQ1, TRPM5, 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
    nsv6620978copy number variation1nstd224human GRCh37 chr11: 2,428,448-2,443,430 , GRCh38.p12 chr11: 2,407,218-2,422,200 TRPM5
    nsv6447429copy number variation1nstd223human GRCh38 chr11: 2,396,261-2,410,524 , GRCh37.p13 chr11: 2,417,491-2,431,754 CD81, TRPM5, 1 more genes
    nsv6445062copy number variation1nstd223human GRCh38 chr11: 2,332,828-2,810,839 , GRCh37.p13 chr11: 2,354,058-2,832,069 RPL26P30, CD81, 7 more genes
    nsv6440391copy number variation1nstd223human GRCh38 chr11: 2,422,165-2,425,318 , GRCh37.p13 chr11: 2,443,395-2,446,548 TRPM5
    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
    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
    nsv6291427copy number variation1nstd102humannot provided GRCh37 chr11: 230,615-5,525,355 , GRCh38.p12 chr11: 230,615-5,504,125 OR52J1P, IFITM1, 255 more genes
    nsv6275182copy number variation1nstd214human GRCh38 chr11: 2,422,013-2,422,072 , GRCh37.p13 chr11: 2,443,243-2,443,302 TRPM5
    nsv6211681insertion1nstd214human GRCh38 chr11: 2,422,013-2,422,013 , GRCh37.p13 chr11: 2,443,243-2,443,243 TRPM5
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