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Items: 1 to 20 of 249

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5949740insertion1nstd209human GRCh38 chr7: 141,614,595-141,614,595 , GRCh37.p13 chr7: 141,314,395-141,314,395 AGK
    nsv5923723copy number variation1nstd209human GRCh38 chr7: 141,578,140-141,584,121 , GRCh37.p13 chr7: 141,277,940-141,283,921 AGK
    nsv5847642copy number variation1nstd209human GRCh38 chr7: 141,577,572-141,583,810 , GRCh37.p13 chr7: 141,277,372-141,283,610 AGK
    nsv5718114mobile element insertion1nstd211human GRCh38 chr7: 141,578,762-141,578,762 , GRCh37.p13 chr7: 141,278,562-141,278,562 AGK
    nsv5713538mobile element insertion2nstd211human GRCh38 chr7: 141,614,609-141,614,609 , GRCh37.p13 chr7: 141,314,409-141,314,409 AGK
    nsv5711898mobile element insertion2nstd211human GRCh38 chr7: 141,605,114-141,605,114 , GRCh37.p13 chr7: 141,304,914-141,304,914 AGK
    nsv5702841mobile element insertion2nstd211human GRCh38 chr7: 141,555,068-141,555,068 , GRCh37.p13 chr7: 141,254,868-141,254,868 AGK
    nsv5626751insertion1nstd207human GRCh38 chr7: 141,614,595-141,614,595 , GRCh37.p13 chr7: 141,314,395-141,314,395 AGK
    nsv5571124copy number variation1nstd207human GRCh38 chr7: 141,578,085-141,584,049 , GRCh37.p13 chr7: 141,277,885-141,283,849 AGK
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5534000insertion1nstd206human GRCh38 chr7: 141,570,235-141,570,273 , GRCh37.p13 chr7: 141,270,035-141,270,073 AGK
    nsv5492771copy number variation1nstd206human GRCh38 chr7: 141,653,982-141,654,053 , GRCh37.p13 chr7: 141,353,782-141,353,853 DENND11, AGK
    nsv5476000copy number variation1nstd206human GRCh38 chr7: 141,578,102-141,584,072 , GRCh37.p13 chr7: 141,277,902-141,283,872 AGK
    nsv5404275mobile element insertion1nstd206human GRCh38 chr7: 141,614,609-141,614,660 , GRCh37.p13 chr7: 141,314,409-141,314,460 AGK
    nsv5399167mobile element insertion1nstd206human GRCh38 chr7: 141,605,114-141,605,165 , GRCh37.p13 chr7: 141,304,914-141,304,965 AGK
    nsv5396208mobile element insertion1nstd206human GRCh38 chr7: 141,555,068-141,555,119 , GRCh37.p13 chr7: 141,254,868-141,254,919 AGK
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5304756copy number variation1nstd204human GRCh38.p13 chr7: 141,578,444-141,584,364 , GRCh37.p13 chr7: 141,278,244-141,284,164 AGK
    nsv5250755copy number variation1nstd204human GRCh38.p13 chr7: 141,578,482-141,583,944 , GRCh37.p13 chr7: 141,278,282-141,283,744 AGK
    nsv5247458copy number variation1nstd204human GRCh38.p13 chr7: 141,578,501-141,584,400 , GRCh37.p13 chr7: 141,278,301-141,284,200 AGK
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