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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
    nsv7074886inversion1nstd229human GRCh38 chr12: 17,805,126-18,607,371 , GRCh37.p13 chr12: 17,958,060-18,760,305 PIK3C2G, NDFIP1P1, 2 more genes
    nsv7059567inversion1nstd229human GRCh38 chr12: 18,069,284-18,081,204 , GRCh37.p13 chr12: 18,222,218-18,234,138 RERGL
    nsv6934835copy number variation1nstd229human GRCh38 chr12: 18,062,581-18,120,620 , GRCh37.p13 chr12: 18,215,515-18,273,554 RERGL
    nsv6927365copy number variation1nstd229human GRCh38 chr12: 18,077,979-18,093,207 , GRCh37.p13 chr12: 18,230,913-18,246,141 RERGL
    nsv6926700copy number variation1nstd229human GRCh38 chr12: 17,955,902-18,116,092 , GRCh37.p13 chr12: 18,108,836-18,269,026 RERGL
    nsv6925902copy number variation1nstd229human GRCh38 chr12: 18,070,858-18,165,234 , GRCh37.p13 chr12: 18,223,792-18,318,168 RERGL
    nsv6924023copy number variation1nstd229human GRCh38 chr12: 18,079,263-18,201,441 , GRCh37.p13 chr12: 18,232,197-18,354,375 RERGL
    nsv6920874copy number variation1nstd229human GRCh38 chr12: 18,056,292-18,090,512 , GRCh37.p13 chr12: 18,209,226-18,243,446 RERGL
    nsv6919771copy number variation1nstd229human GRCh38 chr12: 17,697,182-18,094,934 , GRCh37.p13 chr12: 17,850,116-18,247,868 RERGL
    nsv6918923copy number variation1nstd229human GRCh38 chr12: 18,070,901-18,165,200 , GRCh37.p13 chr12: 18,223,835-18,318,134 RERGL
    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
    nsv6621527copy number variation1nstd224human GRCh37 chr12: 18,234,254-18,307,287 , GRCh38.p12 chr12: 18,081,320-18,154,353 RERGL
    nsv6621433copy number variation2nstd224human GRCh37 chr12: 18,226,996-18,306,480 , GRCh38.p12 chr12: 18,074,062-18,153,546 RERGL
    nsv6581314inversion1nstd223human GRCh38 chr12: 18,069,284-18,081,206 , GRCh37.p13 chr12: 18,222,218-18,234,140 RERGL
    nsv6474008copy number variation1nstd223human GRCh38 chr12: 18,062,581-18,120,620 , GRCh37.p13 chr12: 18,215,515-18,273,554 RERGL
    nsv6473291copy number variation1nstd223human GRCh38 chr12: 18,073,650-18,151,910 , GRCh37.p13 chr12: 18,226,584-18,304,844 RERGL
    nsv6472422copy number variation1nstd223human GRCh38 chr12: 18,070,860-18,165,234 , GRCh37.p13 chr12: 18,223,794-18,318,168 RERGL
    nsv6456481copy number variation1nstd223human GRCh38 chr12: 18,082,801-18,084,400 , GRCh37.p13 chr12: 18,235,735-18,237,334 RERGL
    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
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