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Items: 1 to 20 of 230

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968644insertion1nstd209human GRCh38 chr11: 4,138,073-4,138,073 , GRCh37.p13 chr11: 4,159,303-4,159,303 RRM1
    nsv5967698insertion1nstd209human GRCh38 chr11: 4,099,295-4,099,295 , GRCh37.p13 chr11: 4,120,525-4,120,525 RRM1
    nsv5717735mobile element insertion2nstd211human GRCh38 chr11: 4,136,180-4,136,180 , GRCh37.p13 chr11: 4,157,410-4,157,410 RRM1
    nsv5713880mobile element insertion2nstd211human GRCh38 chr11: 4,096,996-4,096,996 , GRCh37.p13 chr11: 4,118,226-4,118,226 RRM1
    nsv5658141insertion1nstd207human GRCh38 chr11: 4,096,977-4,096,977 , GRCh37.p13 chr11: 4,118,207-4,118,207 RRM1
    nsv5647969insertion1nstd207human GRCh38 chr11: 4,138,067-4,138,067 , GRCh37.p13 chr11: 4,159,297-4,159,297 RRM1
    nsv5596710copy number variation1nstd207human GRCh38 chr11: 4,137,634-4,137,858 , GRCh37.p13 chr11: 4,158,864-4,159,088 RRM1
    nsv5538250insertion1nstd206human GRCh38 chr11: 4,096,996-4,096,998 , GRCh37.p13 chr11: 4,118,226-4,118,228 RRM1
    nsv5534734insertion1nstd206human GRCh38 chr11: 4,096,927-4,096,977 , GRCh37.p13 chr11: 4,118,157-4,118,207 RRM1
    nsv5510372copy number variation1nstd206human GRCh38 chr11: 4,082,000-4,096,000 , GRCh37.p13 chr11: 4,103,230-4,117,230 STIM1, RRM1
    nsv5500666copy number variation1nstd206human GRCh38 chr11: 4,136,180-4,137,021 , GRCh37.p13 chr11: 4,157,410-4,158,251 RRM1
    nsv5373397translocation1nstd200human GRCh38 chr11: 4,493,992-4,493,992 , GRCh38 chr11: 4,132,046-4,132,046 , GRCh37.p13 chr11: 4,515,222-4,515,222 , GRCh37.p13 chr11: 4,153,276-4,153,276 RRM1
    nsv5338807translocation1nstd200human GRCh37 chr11: 4,153,276-4,153,276 , GRCh37 chr11: 4,515,222-4,515,222 , GRCh38.p12 chr11: 4,132,046-4,132,046 , GRCh38.p12 chr11: 4,493,992-4,493,992 RRM1
    nsv5137997mobile element insertion1nstd203human GRCh38 chr11: 4,112,690-4,112,704 , GRCh37.p13 chr11: 4,133,920-4,133,934 RRM1
    nsv5129999mobile element insertion1nstd203human GRCh38 chr11: 4,099,295-4,099,314 , GRCh37.p13 chr11: 4,120,525-4,120,544 RRM1
    nsv5124536mobile element insertion1nstd203human GRCh38 chr11: 4,096,977-4,096,996 , GRCh37.p13 chr11: 4,118,207-4,118,226 RRM1
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4744330copy number variation1nstd199human GRCh37 chr11: 4,158,596-4,158,822 , GRCh38.p12 chr11: 4,137,366-4,137,592 RRM1
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
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