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Items: 1 to 20 of 598

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962057insertion1nstd209human GRCh38 chr6: 119,109,035-119,109,035 , GRCh37.p13 chr6: 119,430,200-119,430,200 FAM184A
    nsv5954826insertion1nstd209human GRCh38 chr6: 118,969,993-118,969,993 , GRCh37.p13 chr6: 119,291,158-119,291,158 FAM184A
    nsv5905949copy number variation1nstd209human GRCh38 chr6: 118,991,354-118,992,549 , GRCh37.p13 chr6: 119,312,519-119,313,714 FAM184A
    nsv5905713copy number variation1nstd209human GRCh38 chr6: 119,016,472-119,016,602 , GRCh37.p13 chr6: 119,337,637-119,337,767 FAM184A
    nsv5896813copy number variation1nstd209human GRCh38 chr6: 119,096,338-119,096,665 , GRCh37.p13 chr6: 119,417,503-119,417,830 FAM184A
    nsv5895810copy number variation1nstd209human GRCh38 chr6: 119,122,841-119,123,081 , GRCh37.p13 chr6: 119,444,006-119,444,246 FAM184A
    nsv5892568copy number variation1nstd209human GRCh38 chr6: 119,015,889-119,016,048 , GRCh37.p13 chr6: 119,337,054-119,337,213 FAM184A
    nsv5890166copy number variation1nstd209human GRCh38 chr6: 119,120,889-119,121,172 , GRCh37.p13 chr6: 119,442,054-119,442,337 FAM184A
    nsv5888224copy number variation1nstd209human GRCh38 chr6: 118,989,498-118,989,558 , GRCh37.p13 chr6: 119,310,663-119,310,723 FAM184A
    nsv5843994copy number variation1nstd209human GRCh38 chr6: 118,991,421-118,992,525 , GRCh37.p13 chr6: 119,312,586-119,313,690 FAM184A
    nsv5689853mobile element insertion1nstd211human GRCh38 chr6: 119,110,546-119,110,546 , GRCh37.p13 chr6: 119,431,711-119,431,711 FAM184A
    nsv5687029mobile element insertion2nstd211human GRCh38 chr6: 119,072,891-119,072,891 , GRCh37.p13 chr6: 119,394,056-119,394,056 FAM184A
    nsv5686543mobile element insertion2nstd211human GRCh38 chr6: 119,109,051-119,109,051 , GRCh37.p13 chr6: 119,430,216-119,430,216 FAM184A
    nsv5682924mobile element insertion2nstd211human GRCh38 chr6: 119,100,655-119,100,655 , GRCh37.p13 chr6: 119,421,820-119,421,820 FAM184A
    nsv5681649mobile element insertion1nstd211human GRCh38 chr6: 119,050,013-119,050,013 , GRCh37.p13 chr6: 119,371,178-119,371,178 FAM184A
    nsv5674881mobile element insertion2nstd211human GRCh38 chr6: 119,079,638-119,079,638 , GRCh37.p13 chr6: 119,400,803-119,400,803 FAM184A
    nsv5642839insertion1nstd207human GRCh38 chr6: 118,970,008-118,970,008 , GRCh37.p13 chr6: 119,291,173-119,291,173 FAM184A
    nsv5641946insertion1nstd207human GRCh38 chr6: 118,989,498-118,989,498 , GRCh37.p13 chr6: 119,310,663-119,310,663 FAM184A
    nsv5638324insertion1nstd207human GRCh38 chr6: 119,109,035-119,109,035 , GRCh37.p13 chr6: 119,430,200-119,430,200 FAM184A
    nsv5638002insertion1nstd207human GRCh38 chr6: 119,100,641-119,100,641 , GRCh37.p13 chr6: 119,421,806-119,421,806 FAM184A
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