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Items: 1 to 20 of 83

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066313inversion1nstd229human GRCh38 chr11: 6,624,146-15,294,249 , GRCh37.p13 chr11: 6,645,377-15,315,795 RNA5SP332, TMEM41B, 163 more genes
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6910369copy number variation1nstd229human GRCh38 chr11: 8,686,227-8,689,969 , GRCh37.p13 chr11: 8,707,774-8,711,516 RPL27A
    nsv6906971copy number variation1nstd229human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 RIC3, LOC644656, 86 more genes
    nsv6901097copy number variation1nstd229human GRCh38 chr11: 8,567,643-8,968,110 , GRCh37.p13 chr11: 8,589,190-8,989,657 SNORA3B, RPL27A, 12 more genes
    nsv6899420copy number variation1nstd229human GRCh38 chr11: 8,689,701-8,694,700 , GRCh37.p13 chr11: 8,711,248-8,716,247 RPL27A, DENND2B
    nsv6578417inversion1nstd223human GRCh38 chr11: 7,263,807-16,565,752 , GRCh37.p13 chr11: 7,285,038-16,587,299 TEAD1, IRAG1, 151 more genes
    nsv6442855copy number variation1nstd223human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 LOC105369149, C11orf16, 86 more genes
    nsv6435810copy number variation1nstd223human GRCh38 chr11: 8,686,227-8,689,967 , GRCh37.p13 chr11: 8,707,774-8,711,514 RPL27A
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv5496888copy number variation1nstd206human GRCh38 chr11: 8,676,695-8,681,756 , GRCh37.p13 chr11: 8,698,242-8,703,303 TRIM66, RPL27A
    nsv4978136copy number variation1nstd200human GRCh38 chr11: 8,686,227-8,689,967 , GRCh37.p13 chr11: 8,707,774-8,711,514 RPL27A
    nsv4978135copy number variation1nstd200human GRCh38 chr11: 8,685,968-8,686,092 , GRCh37.p13 chr11: 8,707,515-8,707,639 RPL27A, SNORA3B
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4565647inversion1nstd166human GRCh37.p13 chr11: 6,776,274-9,026,287 , GRCh38.p12 chr11: 6,755,043-9,004,740 , ZNF215, 61 more genes
    nsv4381760copy number variation1nstd173human GRCh37 chr11: 8,172,302-9,323,454 , GRCh38.p12 chr11: 8,150,755-9,301,907 , KRT8P41, 26 more genes
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv4204280copy number variation1nstd166human GRCh37.p13 chr11: 8,703,000-8,710,000 , GRCh38.p12 chr11: 8,681,453-8,688,453 TRIM66, SNORA3A, 2 more genes
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