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Items: 1 to 20 of 408

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5721538mobile element insertion2nstd211human GRCh38 chr9: 126,456,528-126,456,528 , GRCh37.p13 chr9: 129,218,807-129,218,807 MVB12B
    nsv5707773mobile element insertion1nstd211human GRCh38 chr9: 126,415,415-126,415,415 , GRCh37.p13 chr9: 129,177,694-129,177,694 MVB12B
    nsv5701934mobile element insertion1nstd211human GRCh38 chr9: 126,429,730-126,429,730 , GRCh37.p13 chr9: 129,192,009-129,192,009 MVB12B
    nsv5695538mobile element insertion1nstd211human GRCh38 chr9: 126,493,509-126,493,509 , GRCh37.p13 chr9: 129,255,788-129,255,788 MVB12B
    nsv5597015copy number variation1nstd207human GRCh38 chr9: 126,485,036-126,485,542 , GRCh37.p13 chr9: 129,247,315-129,247,821 MVB12B
    nsv5593004copy number variation1nstd207human GRCh38 chr9: 126,484,619-126,484,943 , GRCh37.p13 chr9: 129,246,898-129,247,222 MVB12B
    nsv5587153copy number variation1nstd207human GRCh38 chr9: 126,484,887-126,484,943 , GRCh37.p13 chr9: 129,247,166-129,247,222 MVB12B
    nsv5556751mobile element insertion1nstd206human GRCh38 chr9: 126,456,528-126,456,579 , GRCh37.p13 chr9: 129,218,807-129,218,858 MVB12B
    nsv5553570insertion1nstd206human GRCh38 chr9: 126,476,077-126,476,102 , GRCh37.p13 chr9: 129,238,356-129,238,381 MVB12B
    nsv5492116copy number variation1nstd206human GRCh38 chr9: 126,499,729-126,499,785 , GRCh37.p13 chr9: 129,262,008-129,262,064 MVB12B
    nsv5491659copy number variation1nstd206human GRCh38 chr9: 126,399,908-126,399,965 , GRCh37.p13 chr9: 129,162,187-129,162,244 MVB12B
    nsv5491279copy number variation1nstd206human GRCh38 chr9: 126,411,849-126,412,169 , GRCh37.p13 chr9: 129,174,128-129,174,448 MVB12B
    nsv5487338copy number variation1nstd206human GRCh38 chr9: 126,376,631-126,378,377 , GRCh37.p13 chr9: 129,138,910-129,140,656 MVB12B
    nsv5483267copy number variation1nstd206human GRCh38 chr9: 126,447,591-126,448,488 , GRCh37.p13 chr9: 129,209,870-129,210,767 MVB12B
    nsv5478669copy number variation1nstd206human GRCh38 chr9: 126,493,546-126,493,597 , GRCh37.p13 chr9: 129,255,825-129,255,876 MVB12B
    nsv5410252mobile element insertion1nstd206human GRCh38 chr9: 126,429,730-126,429,781 , GRCh37.p13 chr9: 129,192,009-129,192,060 MVB12B
    nsv5373113translocation1nstd200human GRCh38 chr9: 126,470,265-126,470,265 , GRCh38 chr9: 126,470,173-126,470,173 , GRCh37.p13 chr9: 129,232,452-129,232,452 , GRCh37.p13 chr9: 129,232,544-129,232,544 MVB12B
    nsv5373112translocation1nstd200human GRCh38 chr9: 126,382,088-126,382,088 , GRCh38 chr9: 126,382,211-126,382,211 , GRCh37.p13 chr9: 129,144,367-129,144,367 , GRCh37.p13 chr9: 129,144,490-129,144,490 MVB12B
    nsv5347390translocation1nstd200human GRCh38 chr8: 144,012,763-144,012,763 , GRCh38 chr9: 126,335,624-126,335,624 , GRCh37.p13 chr8: 145,086,931-145,086,931 , GRCh37.p13 chr8|NW_003315923.1: 351,408-351,408 , GRCh37.p13 chr9: 129,097,903-129,097,903 SPATC1, MVB12B
    nsv5337981translocation1nstd200human GRCh37 chr9: 129,097,903-129,097,903 , GRCh37 chr8: 145,086,931-145,086,931 , GRCh38.p12 chr8: 144,012,763-144,012,763 , GRCh38.p12 chr9: 126,335,624-126,335,624 MVB12B, SPATC1
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