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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5836415copy number variation1nstd209human GRCh38 chr3: 63,925,848-63,927,047 , GRCh37.p13 chr3: 63,911,524-63,912,723 ATXN7
    nsv5693454mobile element insertion1nstd211human GRCh38 chr3: 63,888,960-63,888,960 , GRCh37.p13 chr3: 63,874,636-63,874,636 ATXN7
    nsv5688267mobile element insertion1nstd211human GRCh38 chr3: 63,885,478-63,885,478 , GRCh37.p13 chr3: 63,871,154-63,871,154 ATXN7
    nsv5681522mobile element insertion2nstd211human GRCh38 chr3: 63,873,180-63,873,180 , GRCh37.p13 chr3: 63,858,856-63,858,856 ATXN7
    nsv5675391mobile element insertion2nstd211human GRCh38 chr3: 63,983,298-63,983,298 , GRCh37.p13 chr3: 63,968,974-63,968,974 ATXN7
    nsv5618665insertion1nstd207human GRCh38 chr3: 63,916,544-63,916,544 , GRCh37.p13 chr3: 63,902,220-63,902,220 ATXN7
    nsv5614277insertion1nstd207human GRCh38 chr3: 63,998,847-63,998,847 , GRCh37.p13 chr3: 63,984,523-63,984,523 ATXN7
    nsv5610615insertion1nstd207human GRCh38 chr3: 63,873,164-63,873,164 , GRCh37.p13 chr3: 63,858,840-63,858,840 ATXN7
    nsv5546168insertion1nstd206human GRCh38 chr3: 63,888,960-63,888,997 , GRCh37.p13 chr3: 63,874,636-63,874,673 ATXN7
    nsv5441224copy number variation1nstd206human GRCh38 chr3: 63,903,033-63,903,165 , GRCh37.p13 chr3: 63,888,709-63,888,841 ATXN7
    nsv5413323mobile element insertion1nstd206human GRCh38 chr3: 63,983,298-63,983,349 , GRCh37.p13 chr3: 63,968,974-63,969,025 ATXN7
    nsv5408378mobile element insertion1nstd206human GRCh38 chr3: 63,873,180-63,873,231 , GRCh37.p13 chr3: 63,858,856-63,858,907 ATXN7
    nsv5400157mobile element insertion1nstd206human GRCh38 chr3: 63,885,478-63,885,529 , GRCh37.p13 chr3: 63,871,154-63,871,205 ATXN7
    nsv5351845translocation1nstd200human GRCh38 chr3: 63,876,158-63,876,158 , GRCh38 chr3: 63,874,992-63,874,992 , GRCh37.p13 chr3: 63,860,668-63,860,668 , GRCh37.p13 chr3: 63,861,834-63,861,834 ATXN7
    nsv5305890copy number variation1nstd204human GRCh38.p13 chr3: 63,925,820-63,926,936 , GRCh37.p13 chr3: 63,911,496-63,912,612 ATXN7
    nsv5162529mobile element insertion1nstd203human GRCh38 chr3: 63,876,010-63,876,020 , GRCh37.p13 chr3: 63,861,686-63,861,696 ATXN7
    nsv5086201mobile element insertion1nstd203human GRCh38 chr3: 63,993,660-63,993,674 , GRCh37.p13 chr3: 63,979,336-63,979,350 ATXN7
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , METTL6, 1198 more genes
    nsv4918614copy number variation1nstd200human GRCh38 chr3: 63,929,056-63,931,888 , GRCh37.p13 chr3: 63,914,732-63,917,564 ATXN7
    nsv4918613copy number variation1nstd200human GRCh38 chr3: 63,925,845-63,926,912 , GRCh37.p13 chr3: 63,911,521-63,912,588 ATXN7
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