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Items: 1 to 20 of 174

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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
    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
    nsv7001913copy number variation1nstd229human GRCh38 chr19: 41,754,701-41,761,800 , GRCh37.p13 chr19|NW_004775434.1: 323,740-330,839 , GRCh37.p13 chr19: 42,258,609-42,265,708 CEACAM6, LOC112268252
    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
    nsv6624923copy number variation2nstd224human GRCh37 chr19: 42,262,891-42,280,332 , GRCh38.p12 chr19: 41,758,983-41,776,424 CEACAM6, LOC112268252
    nsv6624738copy number variation1nstd224human GRCh37 chr19: 42,262,891-42,288,577 , GRCh38.p12 chr19: 41,758,983-41,784,670 CEACAM6, LOC112268252
    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
    nsv6520463copy number variation1nstd223human GRCh38 chr19: 41,738,998-41,768,017 , GRCh37.p13 chr19|NW_004775434.1: 308,037-337,056 , GRCh37.p13 chr19: 42,242,918-42,271,926 CEACAM6, LOC112268252
    nsv6515985copy number variation1nstd223human GRCh38 chr19: 41,768,641-41,768,768 , GRCh37.p13 chr19: 42,272,550-42,272,677 , GRCh37.p13 chr19|NW_004775434.1: 337,680-337,807 CEACAM6
    nsv6221277copy number variation1nstd214human GRCh38 chr19: 41,768,641-41,768,767 , GRCh37.p13 chr19: 42,272,550-42,272,676 , GRCh37.p13 chr19|NW_004775434.1: 337,680-337,806 CEACAM6
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 more genes
    nsv6041680copy number variation1nstd212human GRCh38 chr19: 41,750,468-41,786,921 , GRCh37.p13 chr19|NW_004775434.1: 319,507-355,960 , GRCh37.p13 chr19: 42,254,376-42,290,829 CEACAM6, LOC112268252
    nsv6040590copy number variation1nstd212human GRCh38 chr19: 41,768,680-41,768,809 , GRCh37.p13 chr19|NW_004775434.1: 337,719-337,848 , GRCh37.p13 chr19: 42,272,589-42,272,718 CEACAM6
    nsv5946312copy number variation1nstd209human GRCh38 chr19: 41,763,174-41,763,287 , GRCh37.p13 chr19: 42,267,082-42,267,195 , GRCh37.p13 chr19|NW_004775434.1: 332,213-332,326 CEACAM6
    nsv5941544copy number variation1nstd209human GRCh38 chr19: 41,768,641-41,768,767 , GRCh37.p13 chr19|NW_004775434.1: 337,680-337,806 , GRCh37.p13 chr19: 42,272,550-42,272,676 CEACAM6
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