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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7076490inversion1nstd229human GRCh38 chr12: 20,940,376-25,948,754 , GRCh37.p13 chr12: 21,093,310-26,101,687 LOC102724261, IRAG2, 59 more genes
    nsv7058376inversion1nstd229human GRCh38 chr12: 22,669,913-22,670,048 , GRCh37.p13 chr12: 22,822,847-22,822,982 ETNK1
    nsv6937080copy number variation1nstd229human GRCh38 chr12: 22,629,601-22,641,900 , GRCh37.p13 chr12: 22,782,535-22,794,834 ETNK1
    nsv6923291copy number variation1nstd229human GRCh38 chr12: 22,539,898-22,724,093 , GRCh37.p13 chr12: 22,692,832-22,877,027 ETNK1-DT, RPS27P22, 6 more genes
    nsv6921644copy number variation1nstd229human GRCh38 chr12: 22,644,491-22,644,719 , GRCh37.p13 chr12: 22,797,425-22,797,653 ETNK1
    nsv6634456copy number variation1nstd102humanPathogenic GRCh37 chr12: 10,853,887-24,103,810 , GRCh38.p12 chr12: 10,701,288-23,950,876 TAS2R15P, LOC105369673, 209 more genes
    nsv6587091inversion1nstd223human GRCh38 chr12: 22,653,153-22,653,387 , GRCh37.p13 chr12: 22,806,087-22,806,321 ETNK1
    nsv6475135copy number variation1nstd223human GRCh38 chr12: 22,680,901-22,682,600 , GRCh37.p13 chr12: 22,833,835-22,835,534 ETNK1
    nsv6474981copy number variation1nstd223human GRCh38 chr12: 22,663,401-22,664,300 , GRCh37.p13 chr12: 22,816,335-22,817,234 ETNK1
    nsv6472331copy number variation1nstd223human GRCh38 chr12: 22,660,727-22,661,232 , GRCh37.p13 chr12: 22,813,661-22,814,166 ETNK1
    nsv6471688copy number variation1nstd223human GRCh38 chr12: 22,651,159-22,651,479 , GRCh37.p13 chr12: 22,804,093-22,804,413 ETNK1
    nsv6466376copy number variation1nstd223human GRCh38 chr12: 22,663,701-22,665,300 , GRCh37.p13 chr12: 22,816,635-22,818,234 ETNK1
    nsv6465661copy number variation1nstd223human GRCh38 chr12: 22,645,379-22,646,130 , GRCh37.p13 chr12: 22,798,313-22,799,064 ETNK1
    nsv6460572copy number variation1nstd223human GRCh38 chr12: 22,656,922-22,657,305 , GRCh37.p13 chr12: 22,809,856-22,810,239 ETNK1
    nsv6456480copy number variation1nstd223human GRCh38 chr12: 22,641,801-22,642,900 , GRCh37.p13 chr12: 22,794,735-22,795,834 ETNK1
    nsv6314083copy number variation1nstd102humanPathogenic GRCh37 chr12: 17,884,992-26,704,895 , GRCh38.p12 chr12: 17,732,058-26,551,962 SLCO1B1, RERGL, 105 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
    nsv6132232copy number variation1nstd213human GRCh37 chr12: 22,770,000-23,600,001 , GRCh38.p12 chr12: 22,617,066-23,447,067 , ETNK1, 3 more genes
    nsv6132231copy number variation1nstd213human GRCh37 chr12: 21,890,000-23,190,001 , GRCh38.p12 chr12: 21,737,066-23,037,067 C2CD5, C2CD5-AS1, 18 more genes
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