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Items: 1 to 20 of 357

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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
    nsv7093926copy number variation1nstd102humanUncertain significance GRCh37 chr11: 1,774,733-2,019,125 , GRCh38.p12 chr11: 1,753,503-1,997,895 LINC01219, MIR7847, 16 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
    nsv6914170copy number variation1nstd229human GRCh38 chr11: 1,861,871-1,888,302 , GRCh37.p13 chr11: 1,883,101-1,909,532 LSP1, MIR7847
    nsv6912221copy number variation1nstd229human GRCh38 chr11: 1,884,582-1,886,730 , GRCh37.p13 chr11: 1,905,812-1,907,960 LSP1
    nsv6907777copy number variation1nstd229human GRCh38 chr11: 1,875,063-1,875,210 , GRCh37.p13 chr11: 1,896,293-1,896,440 LSP1
    nsv6906593copy number variation1nstd229human GRCh38 chr11: 1,881,337-1,884,124 , GRCh37.p13 chr11: 1,902,567-1,905,354 LSP1
    nsv6905522copy number variation1nstd229human GRCh38 chr11: 1,858,701-1,867,100 , GRCh37.p13 chr11: 1,879,931-1,888,330 MIR4298, LSP1
    nsv6904170copy number variation1nstd229human GRCh38 chr11: 1,856,211-1,862,207 , GRCh37.p13 chr11: 1,877,441-1,883,437 LSP1, MIR4298
    nsv6903560copy number variation1nstd229human GRCh38 chr11: 1,846,525-1,852,676 , GRCh37.p13 chr11: 1,867,755-1,873,906 LOC107984299, LSP1
    nsv6902008copy number variation1nstd229human GRCh38 chr11: 1,846,162-1,862,733 , GRCh37.p13 chr11: 1,867,392-1,883,963 MIR4298, LSP1, 1 more genes
    nsv6901499copy number variation1nstd229human GRCh38 chr11: 1,846,357-1,852,317 , GRCh37.p13 chr11: 1,867,587-1,873,547 LSP1, LOC107984299
    nsv6899602copy number variation1nstd229human GRCh38 chr11: 1,874,601-1,875,800 , GRCh37.p13 chr11: 1,895,831-1,897,030 LSP1
    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
    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
    nsv6444249copy number variation1nstd223human GRCh38 chr11: 1,866,119-1,928,522 , GRCh37.p13 chr11: 1,887,349-1,949,752 MIR7847, LINC01150, 2 more genes
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