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Items: 1 to 20 of 246

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7063078inversion1nstd229human GRCh38 chr8: 30,794,080-30,812,682 , GRCh37.p13 chr8: 30,651,596-30,670,198 PPP2CB
    nsv6852308copy number variation1nstd229human GRCh38 chr8: 30,778,975-30,793,092 , GRCh37.p13 chr8: 30,636,491-30,650,608 PPP2CB
    nsv6841065copy number variation1nstd229human GRCh38 chr8: 30,653,801-30,829,800 , GRCh37.p13 chr8: 30,511,318-30,687,316 PPP2CB, GTF2E2, 5 more genes
    nsv6839985copy number variation1nstd229human GRCh38 chr8: 28,051,949-30,854,206 , GRCh37.p13 chr8: 27,909,466-30,711,722 PPP2CB, RNU6-1218P, 59 more genes
    nsv6637025copy number variation1nstd102humanPathogenic GRCh37 chr8: 26,808,969-38,346,383 , GRCh38.p12 chr8: 26,951,452-38,488,865 LINC02948, LOC105379354, 185 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6557070inversion1nstd223human GRCh38 chr8: 30,805,439-30,806,061 , GRCh37.p13 chr8: 30,662,955-30,663,577 PPP2CB
    nsv6432515copy number variation1nstd223human GRCh38 chr8: 30,778,975-30,793,087 , GRCh37.p13 chr8: 30,636,491-30,650,603 PPP2CB
    nsv6422517copy number variation1nstd223human GRCh38 chr8: 30,697,860-30,950,805 , GRCh37.p13 chr8: 30,555,377-30,808,321 GSR, PPP2CB, 5 more genes
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6245814mobile element insertion1nstd215human GRCh38 chr8: 30,786,509-30,786,509 , GRCh37.p13 chr8: 30,644,025-30,644,025 PPP2CB
    nsv6137272copy number variation1nstd213human GRCh37 chr8: 26,370,000-35,590,001 , GRCh38.p12 chr8: 26,512,484-35,732,483 ADRA1A, CHRNA2, 141 more genes
    nsv6137044copy number variation1nstd213human GRCh37 chr8: 12,460,000-33,310,001 , GRCh38.p12 chr8: 12,602,491-33,452,483 NAT1, ASAH1, 322 more genes
    nsv6136663copy number variation1nstd213human GRCh37 chr8: 30,090,000-31,400,001 , GRCh38.p12 chr8: 30,232,484-31,542,485 GTF2E2, UBXN8, 24 more genes
    nsv6136029copy number variation1nstd213human GRCh37 chr8: 26,360,000-35,600,001 , GRCh38.p12 chr8: 26,502,484-35,742,483 ADRA1A, CHRNA2, 141 more genes
    nsv6080289insertion1nstd212human GRCh38 chr8: 30,786,497-30,786,497 , GRCh37.p13 chr8: 30,644,013-30,644,013 PPP2CB
    nsv6078744insertion1nstd212human GRCh38 chr8: 30,794,467-30,794,467 , GRCh37.p13 chr8: 30,651,983-30,651,983 PPP2CB
    nsv5966696insertion1nstd209human GRCh38 chr8: 30,786,497-30,786,497 , GRCh37.p13 chr8: 30,644,013-30,644,013 PPP2CB
    nsv5950271insertion1nstd209human GRCh38 chr8: 30,784,663-30,784,663 , GRCh37.p13 chr8: 30,642,179-30,642,179 PPP2CB
    nsv5703202mobile element insertion2nstd211human GRCh38 chr8: 30,786,509-30,786,509 , GRCh37.p13 chr8: 30,644,025-30,644,025 PPP2CB
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