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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
    nsv5963183insertion1nstd209human GRCh38 chr8: 73,821,598-73,821,598 , GRCh37.p13 chr8: 74,733,833-74,733,833 UBE2W
    nsv5955042insertion1nstd209human GRCh38 chr8: 73,805,470-73,805,470 , GRCh37.p13 chr8: 74,717,705-74,717,705 UBE2W
    nsv5953935insertion1nstd209human GRCh38 chr8: 73,845,056-73,845,056 , GRCh37.p13 chr8: 74,757,291-74,757,291 UBE2W
    nsv5922186copy number variation1nstd209human GRCh38 chr8: 73,860,411-73,860,543 , GRCh37.p13 chr8: 74,772,646-74,772,778 UBE2W
    nsv5919342copy number variation1nstd209human GRCh38 chr8: 72,905,491-79,590,734 , GRCh37.p13 chr8: 73,817,726-80,502,969 , GYG1P1, 73 more genes
    nsv5909910copy number variation1nstd209human GRCh38 chr8: 73,875,526-73,875,622 , GRCh37.p13 chr8: 74,787,761-74,787,857 UBE2W
    nsv5727358mobile element insertion1nstd211human GRCh38 chr8: 73,863,932-73,863,932 , GRCh37.p13 chr8: 74,776,167-74,776,167 UBE2W
    nsv5700501mobile element insertion2nstd211human GRCh38 chr8: 73,854,222-73,854,222 , GRCh37.p13 chr8: 74,766,457-74,766,457 UBE2W
    nsv5694833mobile element insertion2nstd211human GRCh38 chr8: 73,865,207-73,865,207 , GRCh37.p13 chr8: 74,777,442-74,777,442 UBE2W
    nsv5566146copy number variation1nstd207human GRCh38 chr8: 73,875,526-73,875,622 , GRCh37.p13 chr8: 74,787,761-74,787,857 UBE2W
    nsv5560374inversion1nstd206human GRCh38 chr8: 73,821,220-73,822,339 , GRCh37.p13 chr8: 74,733,455-74,734,574 UBE2W
    nsv5558291sequence alteration1nstd206human GRCh38 chr8: 73,867,422-73,867,448 , GRCh37.p13 chr8: 74,779,657-74,779,683 UBE2W
    nsv5554322sequence alteration1nstd206human GRCh38 chr8: 73,821,596-73,822,030 , GRCh37.p13 chr8: 74,733,831-74,734,265 UBE2W
    nsv5547955insertion1nstd206human GRCh38 chr8: 73,821,597-73,821,602 , GRCh37.p13 chr8: 74,733,832-74,733,837 UBE2W
    nsv5546360insertion1nstd206human GRCh38 chr8: 73,867,422-73,867,422 , GRCh37.p13 chr8: 74,779,657-74,779,657 UBE2W
    nsv5493512copy number variation1nstd206human GRCh38 chr8: 73,779,185-73,781,539 , GRCh37.p13 chr8: 74,691,420-74,693,774 UBE2W
    nsv5479731copy number variation1nstd206human GRCh38 chr8: 73,812,368-73,812,511 , GRCh37.p13 chr8: 74,724,603-74,724,746 UBE2W
    nsv5475224copy number variation1nstd206human GRCh38 chr8: 73,860,411-73,860,552 , GRCh37.p13 chr8: 74,772,646-74,772,787 UBE2W
    nsv5473928copy number variation1nstd206human GRCh38 chr8: 73,875,526-73,875,623 , GRCh37.p13 chr8: 74,787,761-74,787,858 UBE2W
    nsv5403010mobile element insertion1nstd206human GRCh38 chr8: 73,854,222-73,854,273 , GRCh37.p13 chr8: 74,766,457-74,766,508 UBE2W
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