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Items: 1 to 20 of 333

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5974249insertion1nstd209human GRCh38 chr20: 43,682,249-43,682,249 , GRCh37.p13 chr20: 42,310,889-42,310,889 MYBL2
    nsv5947832copy number variation1nstd209human GRCh38 chr20: 43,674,288-43,674,608 , GRCh37.p13 chr20: 42,302,928-42,303,248 MYBL2
    nsv5704741mobile element insertion2nstd211human GRCh38 chr20: 43,682,263-43,682,263 , GRCh37.p13 chr20: 42,310,903-42,310,903 MYBL2
    nsv5701787mobile element insertion1nstd211human GRCh38 chr20: 43,698,080-43,698,080 , GRCh37.p13 chr20: 42,326,720-42,326,720 MYBL2
    nsv5669428insertion1nstd207human GRCh38 chr20: 43,696,486-43,696,486 , GRCh37.p13 chr20: 42,325,126-42,325,126 MYBL2
    nsv5664585insertion1nstd207human GRCh38 chr20: 43,696,733-43,696,733 , GRCh37.p13 chr20: 42,325,373-42,325,373 MYBL2
    nsv5545882insertion1nstd206human GRCh38 chr20: 43,682,249-43,682,249 , GRCh37.p13 chr20: 42,310,889-42,310,889 MYBL2
    nsv5530529copy number variation1nstd206human GRCh38 chr20: 43,689,019-43,690,866 , GRCh37.p13 chr20: 42,317,659-42,319,506 MYBL2
    nsv5523943copy number variation1nstd206human GRCh38 chr20: 43,658,365-43,665,942 , GRCh37.p13 chr20: 42,287,005-42,294,582 MYBL2
    nsv5520905copy number variation1nstd206human GRCh38 chr20: 43,673,910-43,674,609 , GRCh37.p13 chr20: 42,302,550-42,303,249 MYBL2
    nsv5517831copy number variation1nstd206human GRCh38 chr20: 43,652,961-43,756,992 , GRCh37.p13 chr20: 42,281,601-42,385,632 , RPL27AP, 3 more genes
    nsv5517352copy number variation1nstd206human GRCh38 chr20: 43,696,466-43,697,033 , GRCh37.p13 chr20: 42,325,106-42,325,673 MYBL2
    nsv5391077copy number variation3nstd186human GRCh37 chr20: 42,325,116-42,325,653 , GRCh38.p12 chr20: 43,696,476-43,697,013 MYBL2
    nsv5390814copy number variation1nstd186human GRCh37 chr20: 42,324,944-42,325,652 , GRCh38.p12 chr20: 43,696,304-43,697,012 MYBL2
    nsv5325284copy number variation1nstd204human GRCh38.p13 chr20: 43,696,476-43,697,013 , GRCh37.p13 chr20: 42,325,116-42,325,653 MYBL2
    nsv5324090inversion1nstd204human GRCh37.p13 chr20: 35,583,652-44,214,109 , GRCh38.p13 chr20: 36,955,249-45,585,470 , BPI, 180 more genes
    nsv5171889mobile element insertion1nstd203human GRCh38 chr20: 43,670,968-43,670,968 , GRCh37.p13 chr20: 42,299,608-42,299,608 MYBL2
    nsv5166821mobile element insertion1nstd203human GRCh38 chr20: 43,682,249-43,682,263 , GRCh37.p13 chr20: 42,310,889-42,310,903 MYBL2
    nsv5033948inversion1nstd200human GRCh38 chr20: 36,955,253-45,585,464 , GRCh37.p13 chr20: 35,583,656-44,214,103 , EMILIN3, 180 more genes
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