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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
    nsv7074936inversion1nstd229human GRCh38 chr12: 15,135,402-15,135,522 , GRCh37.p13 chr12: 15,288,336-15,288,456 RERG
    nsv7074405inversion1nstd229human GRCh38 chr12: 15,185,117-15,185,206 , GRCh37.p13 chr12: 15,338,051-15,338,140 RERG
    nsv7064011inversion1nstd229human GRCh38 chr12: 11,255,910-17,864,916 , GRCh37.p13 chr12: 11,408,826-18,017,850 MGP, MIR3974, 108 more genes
    nsv7060662inversion1nstd229human GRCh38 chr12: 15,114,246-15,116,168 , GRCh37.p13 chr12: 15,267,180-15,269,102 RERG
    nsv6937694copy number variation1nstd229human GRCh38 chr12: 15,110,154-15,117,833 , GRCh37.p13 chr12: 15,263,088-15,270,767 RERG
    nsv6935687copy number variation1nstd229human GRCh38 chr12: 15,144,802-15,145,508 , GRCh37.p13 chr12: 15,297,736-15,298,442 RERG
    nsv6935494copy number variation1nstd229human GRCh38 chr12: 15,178,510-15,183,814 , GRCh37.p13 chr12: 15,331,444-15,336,748 RERG
    nsv6935200copy number variation1nstd229human GRCh38 chr12: 15,107,301-15,207,200 , GRCh37.p13 chr12: 15,260,235-15,360,134 RERG-AS1, RERG
    nsv6934408copy number variation1nstd229human GRCh38 chr12: 15,178,079-15,186,495 , GRCh37.p13 chr12: 15,331,013-15,339,429 RERG
    nsv6931254copy number variation1nstd229human GRCh38 chr12: 15,197,361-15,204,656 , GRCh37.p13 chr12: 15,350,295-15,357,590 RERG
    nsv6929436copy number variation1nstd229human GRCh38 chr12: 15,187,735-15,190,337 , GRCh37.p13 chr12: 15,340,669-15,343,271 RERG
    nsv6925860copy number variation1nstd229human GRCh38 chr12: 15,165,601-15,168,100 , GRCh37.p13 chr12: 15,318,535-15,321,034 RERG
    nsv6921999copy number variation1nstd229human GRCh38 chr12: 15,170,214-15,277,457 , GRCh37.p13 chr12: 15,323,148-15,430,391 METTL8P1, RERG
    nsv6921757copy number variation1nstd229human GRCh38 chr12: 15,178,208-15,182,837 , GRCh37.p13 chr12: 15,331,142-15,335,771 RERG
    nsv6919701copy number variation1nstd229human GRCh38 chr12: 15,163,701-15,202,300 , GRCh37.p13 chr12: 15,316,635-15,355,234 RERG
    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
    nsv6593098inversion1nstd223human GRCh38 chr12: 15,114,246-15,116,166 , GRCh37.p13 chr12: 15,267,180-15,269,100 RERG
    nsv6470728copy number variation1nstd223human GRCh38 chr12: 15,112,901-15,114,600 , GRCh37.p13 chr12: 15,265,835-15,267,534 RERG
    nsv6467747copy number variation1nstd223human GRCh38 chr12: 15,211,850-15,213,946 , GRCh37.p13 chr12: 15,364,784-15,366,880 RERG
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