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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095480copy number variation4nstd102humanUncertain significance GRCh37 chr19: 39,904,727-42,931,301 , GRCh38.p12 chr19: 39,414,087-42,427,149 CYP2B6, EID2B, 140 more genes
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 more genes
    nsv7071361inversion1nstd229human GRCh38 chr19: 39,004,066-42,402,005 , GRCh37.p13 chr19: 39,494,706-42,906,157 RAB4B, RABAC1, 160 more genes
    nsv7068288inversion1nstd229human GRCh38 chr19: 39,023,970-42,945,419 , GRCh37.p13 chr19: 39,514,610-43,449,571 MIR4530, RNU6-195P, 178 more genes
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 more genes
    nsv7010550copy number variation1nstd229human GRCh38 chr19: 42,152,651-42,434,835 , GRCh37.p13 chr19: 42,656,803-42,938,987 CNFN, ERF, 14 more genes
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7005469copy number variation1nstd229human GRCh38 chr19: 42,237,601-42,255,300 , GRCh37.p13 chr19: 42,741,753-42,759,452 ERF, GSK3A
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6596591inversion1nstd223human GRCh38 chr19: 41,749,358-42,444,703 , GRCh37.p13 chr19: 42,514,712-42,948,855 CXCL17, CNFN, 32 more genes
    nsv6595891inversion1nstd223human GRCh38 chr19: 41,749,077-42,444,707 , GRCh37.p13 chr19: 42,514,712-42,948,859 POU2F2, MIR4323, 32 more genes
    nsv6595594inversion1nstd223human GRCh38 chr19: 41,797,668-42,527,301 , GRCh37.p13 chr19: 42,514,712-43,031,453 GRIK5, CEACAM1, 34 more genes
    nsv6310689copy number variation1nstd102humanPathogenic GRCh37 chr19: 42,703,590-42,778,729 , GRCh38.p12 chr19: 42,199,438-42,274,577 ERF, DEDD2, 3 more genes
    nsv6144516copy number variation1nstd206human GRCh38 chr19: 42,208,874-42,304,874 , GRCh37.p13 chr19: 42,713,026-42,809,026 ERF, GSK3A, 5 more genes
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 more genes
    nsv6133474copy number variation1nstd213human GRCh37 chr19: 42,350,000-49,650,001 , GRCh38.p12 chr19: 41,845,937-49,146,744 , APOC1, 343 more genes
    nsv5944073copy number variation1nstd209human GRCh38 chr19: 42,242,322-42,266,502 , GRCh37.p13 chr19: 42,746,474-42,770,654 ERF, GSK3A
    nsv5884317copy number variation1nstd209human GRCh38 chr19: 42,242,378-42,253,700 , GRCh37.p13 chr19: 42,746,530-42,757,852 GSK3A, ERF
    nsv5564524copy number variation1nstd102humanPathogenic GRCh38 chr19: 42,198,610-42,249,880 , GRCh37.p13 chr19: 42,702,762-42,754,032 ERF, ZNF526, 2 more genes
    nsv5564519copy number variation1nstd102humanPathogenic GRCh38 chr19: 41,987,984-42,252,574 , GRCh37.p13 chr19: 42,514,712-42,756,726 GRIK5, DEDD2, 8 more genes
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