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Items: 1 to 20 of 369

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128156copy number variation1nstd186human GRCh37 chr20: 37,119,294-37,119,369 , GRCh38.p12 chr20: 38,490,651-38,490,726 RALGAPB
    nsv6124308copy number variation1nstd186human GRCh37 chr20: 37,139,270-37,139,569 , GRCh38.p12 chr20: 38,510,627-38,510,926 RALGAPB
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5973078insertion1nstd209human GRCh38 chr20: 38,482,019-38,482,019 , GRCh37.p13 chr20: 37,110,662-37,110,662 RALGAPB
    nsv5957659copy number variation1nstd209human GRCh38 chr20: 38,510,613-38,510,925 , GRCh37.p13 chr20: 37,139,256-37,139,568 RALGAPB
    nsv5955107copy number variation1nstd209human GRCh38 chr20: 38,490,650-38,490,725 , GRCh37.p13 chr20: 37,119,293-37,119,368 RALGAPB
    nsv5728836mobile element insertion1nstd211human GRCh38 chr20: 38,496,217-38,496,217 , GRCh37.p13 chr20: 37,124,860-37,124,860 RALGAPB
    nsv5720702mobile element insertion1nstd211human GRCh38 chr20: 38,476,825-38,476,825 , GRCh37.p13 chr20: 37,105,468-37,105,468 RALGAPB
    nsv5712322mobile element insertion1nstd211human GRCh38 chr20: 38,508,834-38,508,834 , GRCh37.p13 chr20: 37,137,477-37,137,477 RALGAPB
    nsv5702572mobile element insertion1nstd211human GRCh38 chr20: 38,482,032-38,482,032 , GRCh37.p13 chr20: 37,110,675-37,110,675 RALGAPB
    nsv5667646insertion1nstd207human GRCh38 chr20: 38,482,019-38,482,019 , GRCh37.p13 chr20: 37,110,662-37,110,662 RALGAPB
    nsv5594659copy number variation1nstd207human GRCh38 chr20: 38,510,613-38,510,925 , GRCh37.p13 chr20: 37,139,256-37,139,568 RALGAPB
    nsv5592184copy number variation1nstd207human GRCh38 chr20: 38,490,650-38,490,725 , GRCh37.p13 chr20: 37,119,293-37,119,368 RALGAPB
    nsv5561058mobile element insertion1nstd206human GRCh38 chr20: 38,496,217-38,496,268 , GRCh37.p13 chr20: 37,124,860-37,124,911 RALGAPB
    nsv5527382copy number variation1nstd206human GRCh38 chr20: 38,490,651-38,490,726 , GRCh37.p13 chr20: 37,119,294-37,119,369 RALGAPB
    nsv5526149copy number variation1nstd206human GRCh38 chr20: 38,510,627-38,510,926 , GRCh37.p13 chr20: 37,139,270-37,139,569 RALGAPB
    nsv5524303copy number variation1nstd206human GRCh38 chr20: 38,482,556-38,482,935 , GRCh37.p13 chr20: 37,111,199-37,111,578 RALGAPB
    nsv5431414mobile element insertion1nstd206human GRCh38 chr20: 38,482,032-38,482,083 , GRCh37.p13 chr20: 37,110,675-37,110,726 RALGAPB
    nsv5383398mobile element deletion2nstd186human GRCh37 chr20: 37,139,270-37,139,569 , GRCh38.p12 chr20: 38,510,627-38,510,926 RALGAPB
    nsv5328319translocation1nstd204human GRCh38.p13 chr20: 38,490,651-38,490,651 , GRCh38.p13 chr20: 38,490,726-38,490,726 , GRCh37.p13 chr20: 37,119,294-37,119,294 , GRCh37.p13 chr20: 37,119,369-37,119,369 RALGAPB
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