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Items: 1 to 20 of 662

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5927397copy number variation1nstd209human GRCh38 chr9: 134,368,937-134,369,128 , GRCh37.p13 chr9: 137,260,783-137,260,974 RXRA
    nsv5911960copy number variation1nstd209human GRCh38 chr9: 134,384,082-134,384,191 , GRCh37.p13 chr9: 137,275,928-137,276,037 RXRA
    nsv5909909copy number variation1nstd209human GRCh38 chr9: 134,431,695-134,431,831 , GRCh37.p13 chr9: 137,323,541-137,323,677 RXRA
    nsv5699727mobile element insertion2nstd211human GRCh38 chr9: 134,397,517-134,397,517 , GRCh37.p13 chr9: 137,289,363-137,289,363 RXRA
    nsv5642267insertion1nstd207human GRCh38 chr9: 134,369,033-134,369,033 , GRCh37.p13 chr9: 137,260,879-137,260,879 RXRA
    nsv5641765insertion1nstd207human GRCh38 chr9: 134,369,295-134,369,295 , GRCh37.p13 chr9: 137,261,141-137,261,141 RXRA
    nsv5629849insertion1nstd207human GRCh38 chr9: 134,394,154-134,394,154 , GRCh37.p13 chr9: 137,286,000-137,286,000 RXRA
    nsv5625276insertion1nstd207human GRCh38 chr9: 134,376,627-134,376,627 , GRCh37.p13 chr9: 137,268,473-137,268,473 RXRA
    nsv5599918copy number variation1nstd207human GRCh38 chr9: 134,422,587-134,422,640 , GRCh37.p13 chr9: 137,314,433-137,314,486 RXRA
    nsv5588124copy number variation1nstd207human GRCh38 chr9: 134,428,394-134,428,494 , GRCh37.p13 chr9: 137,320,240-137,320,340 RXRA
    nsv5485128copy number variation1nstd206human GRCh38 chr9: 134,431,697-134,431,832 , GRCh37.p13 chr9: 137,323,543-137,323,678 RXRA
    nsv5484802copy number variation1nstd206human GRCh38 chr9: 134,326,497-134,326,560 , GRCh37.p13 chr9|NW_004070868.1: 140,121-140,184 , GRCh37.p13 chr9: 137,218,343-137,218,406 RXRA
    nsv5407030mobile element insertion1nstd206human GRCh38 chr9: 134,397,517-134,397,568 , GRCh37.p13 chr9: 137,289,363-137,289,414 RXRA
    nsv5379545translocation1nstd200human GRCh38 chr9: 134,339,077-134,339,077 , GRCh38 chr14: 79,372,830-79,372,830 , GRCh37.p13 chr9|NW_004070868.1: 152,701-152,701 , GRCh37.p13 chr14: 79,839,173-79,839,173 , GRCh37.p13 chr9: 137,230,923-137,230,923 NRXN3, RXRA
    nsv5373179translocation1nstd200human GRCh38 chr9: 134,431,697-134,431,697 , GRCh38 chr9: 134,431,832-134,431,832 , GRCh37.p13 chr9: 137,323,543-137,323,543 , GRCh37.p13 chr9: 137,323,678-137,323,678 RXRA
    nsv5373178translocation1nstd200human GRCh38 chr9: 134,381,192-134,381,192 , GRCh38 chr9: 134,381,697-134,381,697 , GRCh37.p13 chr9: 137,273,543-137,273,543 , GRCh37.p13 chr9: 137,273,038-137,273,038 RXRA
    nsv5373177translocation1nstd200human GRCh38 chr9: 134,326,497-134,326,497 , GRCh38 chr9: 134,326,560-134,326,560 , GRCh37.p13 chr9|NW_004070868.1: 140,121-140,121 , GRCh37.p13 chr9: 137,218,343-137,218,343 , GRCh37.p13 chr9|NW_004070868.1: 140,184-140,184 , GRCh37.p13 chr9: 137,218,406-137,218,406 RXRA
    nsv5335588translocation1nstd200human GRCh37 chr9: 137,230,917-137,230,917 , GRCh37 chr14: 79,839,173-79,839,173 , GRCh38.p12 chr14: 79,372,830-79,372,830 , GRCh38.p12 chr9: 134,339,071-134,339,071 NRXN3, RXRA
    nsv5322198translocation1nstd204human GRCh37.p13 chr9|NW_004070868.1: 152,701-152,701 , GRCh37.p13 chr14: 79,839,173-79,839,173 , GRCh37.p13 chr9: 137,230,923-137,230,923 , GRCh38.p13 chr14: 79,372,830-79,372,830 , GRCh38.p13 chr9: 134,339,077-134,339,077 RXRA, NRXN3
    nsv5319079copy number variation1nstd204human GRCh38.p13 chr9: 134,404,916-134,459,026 , GRCh37.p13 chr9: 137,296,762-137,350,872 RXRA
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