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Items: 1 to 20 of 260

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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
    nsv7095210copy number variation1nstd102humanUncertain significance GRCh37 chr19: 42,388,535-42,402,756 , GRCh38.p12 chr19: 41,884,468-41,898,607 ARHGEF1
    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
    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
    nsv6999226copy number variation1nstd229human GRCh38 chr19: 41,898,587-41,901,885 , GRCh37.p13 chr19|NW_004775434.1: 467,626-470,924 , GRCh37.p13 chr19: 42,402,736-42,406,035 ARHGEF1
    nsv6998704copy number variation1nstd229human GRCh38 chr19: 41,756,999-41,884,097 , GRCh37.p13 chr19|NW_004775434.1: 326,038-453,136 , GRCh37.p13 chr19: 42,260,907-42,388,164 CEACAM6, MIR6797, 9 more genes
    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
    nsv6531074copy number variation1nstd223human GRCh38 chr19: 41,882,510-41,882,994 , GRCh37.p13 chr19: 42,386,577-42,387,061 , GRCh37.p13 chr19|NW_004775434.1: 451,549-452,033 ARHGEF1
    nsv6306204copy number variation1nstd186human GRCh37 chr19: 42,398,821-42,399,149 , GRCh38.p12 chr19: 41,894,748-41,895,076 ARHGEF1
    nsv6227020copy number variation1nstd214human GRCh38 chr19: 41,893,831-41,893,927 , GRCh37.p13 chr19: 42,397,902-42,397,998 , GRCh37.p13 chr19|NW_004775434.1: 462,870-462,966 ARHGEF1
    nsv6226639copy number variation1nstd214human GRCh38 chr19: 41,894,856-41,894,959 , GRCh37.p13 chr19|NW_004775434.1: 463,895-463,998 , GRCh37.p13 chr19: 42,398,929-42,399,032 ARHGEF1
    nsv6210726copy number variation1nstd214human GRCh38 chr19: 41,894,805-41,894,907 , GRCh37.p13 chr19: 42,398,878-42,398,980 , GRCh37.p13 chr19|NW_004775434.1: 463,844-463,946 ARHGEF1
    nsv6145216copy number variation1nstd206human GRCh38 chr19: 41,894,698-41,895,195 , GRCh37.p13 chr19: 42,398,771-42,399,268 , GRCh37.p13 chr19|NW_004775434.1: 463,737-464,234 ARHGEF1
    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
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