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Items: 1 to 20 of 277

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961846insertion1nstd209human GRCh38 chr3: 48,481,441-48,481,441 , GRCh37.p13 chr3: 48,522,850-48,522,850 SHISA5
    nsv5951302insertion1nstd209human GRCh38 chr3: 48,499,782-48,499,782 , GRCh37.p13 chr3: 48,537,216-48,537,216 SHISA5
    nsv5906516copy number variation1nstd209human GRCh38 chr3: 48,492,311-48,496,057 , GRCh37.p13 chr: NaN-NaN SHISA5
    nsv5903767copy number variation1nstd209human GRCh38 chr3: 48,492,350-48,496,171 , GRCh37.p13 chr: NaN-NaN SHISA5
    nsv5892773copy number variation1nstd209human GRCh38 chr3: 48,483,324-48,483,891 , GRCh37.p13 chr3: 48,524,743-48,525,262 SHISA5
    nsv5889250copy number variation1nstd209human GRCh38 chr3: 48,497,341-48,497,400 , GRCh37.p13 chr3: 48,534,774-48,534,833 SHISA5
    nsv5836314copy number variation1nstd209human GRCh38 chr3: 48,492,316-48,496,167 , GRCh37.p13 chr: NaN-NaN SHISA5
    nsv5724034mobile element insertion1nstd211human GRCh38 chr3: 48,472,753-48,472,753 , GRCh37.p13 chr3: 48,514,162-48,514,162 SHISA5
    nsv5673729copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,507,870-50,340,407 , GRCh38.p12 chr3: 48,466,471-50,302,976 SEMA3B-AS1, GNAT1, 87 more genes
    nsv5618732insertion1nstd207human GRCh38 chr3: 48,481,441-48,481,441 , GRCh37.p13 chr3: 48,522,850-48,522,850 SHISA5
    nsv5617293insertion1nstd207human GRCh38 chr3: 48,483,742-48,483,742 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN SHISA5
    nsv5614482insertion1nstd207human GRCh38 chr3: 48,486,344-48,486,344 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN SHISA5
    nsv5609835insertion1nstd207human GRCh38 chr3: 48,486,260-48,486,260 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN SHISA5
    nsv5608319insertion1nstd207human GRCh38 chr3: 48,486,239-48,486,239 , GRCh37.p13 chr3: 48,527,611-48,527,611 SHISA5
    nsv5608018insertion1nstd207human GRCh38 chr3: 48,499,782-48,499,782 , GRCh37.p13 chr3: 48,537,216-48,537,216 SHISA5
    nsv5581455copy number variation1nstd207human GRCh38 chr3: 48,492,350-48,496,171 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN SHISA5
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5553510insertion1nstd206human GRCh38 chr3: 48,486,260-48,486,290 , GRCh37.p13 chr: NaN-NaN SHISA5
    nsv5451362copy number variation1nstd206human GRCh38 chr3: 48,491,970-48,496,165 , GRCh37.p13 chr: NaN-NaN SHISA5
    nsv5441716copy number variation1nstd206human GRCh38 chr3: 48,488,475-48,497,525 , GRCh37.p13 chr3: 48,529,728-48,534,958 SHISA5
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