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Items: 1 to 20 of 401

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5954534insertion1nstd209human GRCh38 chr4: 89,737,277-89,737,277 , GRCh37.p13 chr4: 90,658,428-90,658,428 SNCA
    nsv5907258copy number variation1nstd209human GRCh38 chr4: 87,165,110-92,683,258 , GRCh37.p13 chr4: 88,086,262-93,604,409 HSP90AB3P, SPP1, 61 more genes
    nsv5895781copy number variation1nstd209human GRCh38 chr4: 89,756,058-89,758,339 , GRCh37.p13 chr4: 90,677,209-90,679,490 SNCA
    nsv5893886copy number variation1nstd209human GRCh38 chr4: 89,727,662-89,727,753 , GRCh37.p13 chr4: 90,648,813-90,648,904 SNCA
    nsv5891248copy number variation1nstd209human GRCh38 chr4: 89,820,225-89,820,982 , GRCh37.p13 chr4: 90,741,376-90,742,133 SNCA
    nsv5840178copy number variation1nstd209human GRCh38 chr4: 89,756,054-89,758,053 , GRCh37.p13 chr4: 90,677,205-90,679,204 SNCA
    nsv5726253mobile element insertion2nstd211human GRCh38 chr4: 89,785,648-89,785,648 , GRCh37.p13 chr4: 90,706,799-90,706,799 SNCA
    nsv5674230copy number variation1nstd102humanPathogenic GRCh37 chr4: 90,647,764-90,758,128 , GRCh38.p12 chr4: 89,726,613-89,836,977 SNCA, SNCA-AS1
    nsv5617482insertion1nstd207human GRCh38 chr4: 89,821,323-89,821,323 , GRCh37.p13 chr4: 90,742,474-90,742,474 SNCA
    nsv5570363copy number variation1nstd207human GRCh38 chr4: 89,727,662-89,727,753 , GRCh37.p13 chr4: 90,648,813-90,648,904 SNCA
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5559505mobile element insertion1nstd206human GRCh38 chr4: 89,785,648-89,785,699 , GRCh37.p13 chr4: 90,706,799-90,706,850 SNCA
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5469413copy number variation1nstd206human GRCh38 chr4: 89,727,663-89,727,754 , GRCh37.p13 chr4: 90,648,814-90,648,905 SNCA
    nsv5465172copy number variation1nstd206human GRCh38 chr4: 89,819,138-89,820,441 , GRCh37.p13 chr4: 90,740,289-90,741,592 SNCA
    nsv5464210copy number variation1nstd206human GRCh38 chr4: 89,736,689-89,738,493 , GRCh37.p13 chr4: 90,657,840-90,659,644 SNCA
    nsv5463765copy number variation1nstd206human GRCh38 chr4: 89,736,342-89,738,562 , GRCh37.p13 chr4: 90,657,493-90,659,713 SNCA
    nsv5386619copy number variation1nstd186human GRCh37 chr4: 90,742,350-90,742,450 , GRCh38.p12 chr4: 89,821,199-89,821,299 SNCA
    nsv5367656translocation1nstd200human GRCh38 chr4: 89,876,764-89,876,764 , GRCh38 chr4: 89,793,998-89,793,998 , GRCh37.p13 chr4: 90,715,149-90,715,149 , GRCh37.p13 chr4: 90,797,915-90,797,915 SNCA
    nsv5367655translocation1nstd200human GRCh38 chr4: 89,790,631-89,790,631 , GRCh38 chr4: 89,876,766-89,876,766 , GRCh37.p13 chr4: 90,711,782-90,711,782 , GRCh37.p13 chr4: 90,797,917-90,797,917 SNCA
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