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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980450copy number variation1nstd102humanPathogenic GRCh37 chr12: 46,150,008-46,321,670 , GRCh38.p12 chr12: 45,756,225-45,927,887 SCAF11, ARID2, 3 more genes
    nsv5980443copy number variation1nstd102humanPathogenic GRCh37 chr12: 46,168,172-46,304,719 , GRCh38.p12 chr12: 45,774,389-45,910,936 KNOP1P2, ARID2, 2 more genes
    nsv5972601insertion1nstd209human GRCh38 chr12: 45,899,671-45,899,671 , GRCh37.p13 chr12: 46,293,454-46,293,454 ARID2
    nsv5944535copy number variation1nstd209human GRCh38 chr12: 45,842,005-45,843,285 , GRCh37.p13 chr12: 46,235,788-46,237,068 ARID2, LOC105369745
    nsv5941966copy number variation1nstd209human GRCh38 chr12: 45,766,848-45,766,912 , GRCh37.p13 chr12: 46,160,631-46,160,695 ARID2
    nsv5932231copy number variation1nstd209human GRCh38 chr12: 45,898,995-45,899,127 , GRCh37.p13 chr12: 46,292,778-46,292,910 ARID2
    nsv5852623copy number variation1nstd209human GRCh38 chr12: 45,757,009-45,759,243 , GRCh37.p13 chr12: 46,150,792-46,153,026 ARID2
    nsv5712424mobile element insertion2nstd211human GRCh38 chr12: 45,894,850-45,894,850 , GRCh37.p13 chr12: 46,288,633-46,288,633 ARID2
    nsv5706811mobile element insertion1nstd211human GRCh38 chr12: 45,738,779-45,738,779 , GRCh37.p13 chr12: 46,132,562-46,132,562 ARID2
    nsv5706425mobile element insertion1nstd211human GRCh38 chr12: 45,799,024-45,799,024 , GRCh37.p13 chr12: 46,192,807-46,192,807 ARID2
    nsv5703475mobile element insertion1nstd211human GRCh38 chr12: 45,882,932-45,882,932 , GRCh37.p13 chr12: 46,276,715-46,276,715 ARID2
    nsv5694541mobile element insertion2nstd211human GRCh38 chr12: 45,781,383-45,781,383 , GRCh37.p13 chr12: 46,175,166-46,175,166 ARID2
    nsv5660342insertion1nstd207human GRCh38 chr12: 45,899,711-45,899,711 , GRCh37.p13 chr12: 46,293,494-46,293,494 ARID2
    nsv5649534insertion1nstd207human GRCh38 chr12: 45,781,372-45,781,372 , GRCh37.p13 chr12: 46,175,155-46,175,155 ARID2
    nsv5564512copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 37,873,948-49,578,619 , GRCh38.p12 chr12: 37,480,146-49,184,836 ADCY6, ABCD2, 187 more genes
    nsv5554374sequence alteration1nstd206human GRCh38 chr12: 45,843,286-45,843,286 , GRCh37.p13 chr12: 46,237,069-46,237,069 ARID2, LOC105369745
    nsv5553315insertion1nstd206human GRCh38 chr12: 45,843,286-45,843,286 , GRCh37.p13 chr12: 46,237,069-46,237,069 LOC105369745, ARID2
    nsv5551480insertion1nstd206human GRCh38 chr12: 45,787,557-45,787,585 , GRCh37.p13 chr12: 46,181,340-46,181,368 ARID2
    nsv5510310copy number variation1nstd206human GRCh38 chr12: 45,752,388-45,753,518 , GRCh37.p13 chr12: 46,146,171-46,147,301 ARID2
    nsv5501086copy number variation1nstd206human GRCh38 chr12: 45,780,914-45,781,373 , GRCh37.p13 chr12: 46,174,697-46,175,156 ARID2
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