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Items: 1 to 20 of 372

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963942insertion1nstd209human GRCh38 chr7: 129,836,879-129,836,879 , GRCh37.p13 chr7: 129,476,719-129,476,719 UBE2H
    nsv5923118copy number variation1nstd209human GRCh38 chr7: 129,904,929-129,906,032 , GRCh37.p13 chr7: 129,544,769-129,545,872 UBE2H
    nsv5919300copy number variation1nstd209human GRCh38 chr7: 129,939,855-129,949,054 , GRCh37.p13 chr7: 129,579,695-129,588,894 UBE2H
    nsv5909271copy number variation1nstd209human GRCh38 chr7: 129,942,261-129,942,338 , GRCh37.p13 chr7: 129,582,101-129,582,178 UBE2H
    nsv5866681copy number variation1nstd209human GRCh38 chr7: 129,902,222-129,903,321 , GRCh37.p13 chr7: 129,542,062-129,543,161 UBE2H
    nsv5866189copy number variation1nstd209human GRCh38 chr7: 129,939,606-129,940,605 , GRCh37.p13 chr7: 129,579,446-129,580,445 UBE2H
    nsv5860140copy number variation1nstd209human GRCh38 chr7: 129,904,822-129,906,021 , GRCh37.p13 chr7: 129,544,662-129,545,861 UBE2H
    nsv5859312copy number variation1nstd209human GRCh38 chr7: 129,939,993-129,949,076 , GRCh37.p13 chr7: 129,579,833-129,588,916 UBE2H
    nsv5847729copy number variation1nstd209human GRCh38 chr7: 129,855,621-129,856,970 , GRCh37.p13 chr7: 129,495,461-129,496,810 UBE2H
    nsv5716262mobile element insertion1nstd211human GRCh38 chr7: 129,867,717-129,867,717 , GRCh37.p13 chr7: 129,507,557-129,507,557 UBE2H
    nsv5708306mobile element insertion1nstd211human GRCh38 chr7: 129,929,496-129,929,496 , GRCh37.p13 chr7: 129,569,336-129,569,336 UBE2H
    nsv5704457mobile element insertion2nstd211human GRCh38 chr7: 129,944,909-129,944,909 , GRCh37.p13 chr7: 129,584,749-129,584,749 UBE2H
    nsv5702041mobile element insertion2nstd211human GRCh38 chr7: 129,907,350-129,907,350 , GRCh37.p13 chr7: 129,547,190-129,547,190 UBE2H
    nsv5640081insertion1nstd207human GRCh38 chr7: 129,944,894-129,944,894 , GRCh37.p13 chr7: 129,584,734-129,584,734 UBE2H
    nsv5638894insertion1nstd207human GRCh38 chr7: 129,886,017-129,886,017 , GRCh37.p13 chr7: 129,525,857-129,525,857 UBE2H
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5493698copy number variation1nstd206human GRCh38 chr7: 129,926,469-129,926,734 , GRCh37.p13 chr7: 129,566,309-129,566,574 UBE2H
    nsv5493287copy number variation1nstd206human GRCh38 chr7: 129,926,094-129,942,685 , GRCh37.p13 chr7: 129,565,934-129,582,525 UBE2H
    nsv5490964copy number variation1nstd206human GRCh38 chr7: 129,911,291-129,932,645 , GRCh37.p13 chr7: 129,551,131-129,572,485 UBE2H
    nsv5476850copy number variation1nstd206human GRCh38 chr7: 129,904,929-129,906,033 , GRCh37.p13 chr7: 129,544,769-129,545,873 UBE2H
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