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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095718copy number variation1nstd102humanPathogenic GRCh37 chr19: 45,451,736-45,452,506 , GRCh38.p12 chr19: 44,948,479-44,949,249 APOC4-APOC2, APOC2
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 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
    nsv7066137inversion1nstd229human GRCh38 chr19: 43,668,049-45,225,177 , GRCh37.p13 chr19: 44,172,201-45,728,435 LOC107985306, LYPD5, 67 more genes
    nsv7059316inversion1nstd229human GRCh38 chr19: 43,396,877-48,200,638 , GRCh37.p13 chr19: 43,901,029-48,703,895 GEMIN7, ZNF229, 212 more genes
    nsv7017140copy number variation1nstd229human GRCh38 chr19: 44,895,100-44,984,838 , GRCh37.p13 chr19: 45,398,357-45,488,096 APOC4-APOC2, APOC2, 6 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
    nsv7004523copy number variation1nstd229human GRCh38 chr19: 44,947,303-44,949,248 , GRCh37.p13 chr19: 45,450,560-45,452,505 APOC4-APOC2, APOC2
    nsv6999525copy number variation1nstd229human GRCh38 chr19: 44,945,580-44,972,176 , GRCh37.p13 chr19: 45,448,837-45,475,433 APOC4, APOC2, 2 more genes
    nsv6526884copy number variation1nstd223human GRCh38 chr19: 44,943,920-44,945,847 , GRCh37.p13 chr19: 45,447,177-45,449,104 APOC2, APOC4-APOC2, 1 more genes
    nsv6523815copy number variation1nstd223human GRCh38 chr19: 44,276,620-45,370,613 , GRCh37.p13 chr19: 44,780,773-45,873,871 APOE, CEACAM16, 48 more genes
    nsv6314081copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,074,342-46,133,841 , GRCh38.p12 chr19: 44,571,096-45,630,583 EXOC3L2, APOE, 50 more genes
    nsv6218664copy number variation1nstd214human GRCh38 chr19: 44,948,974-44,949,084 , GRCh37.p13 chr19: 45,452,231-45,452,341 APOC4-APOC2, APOC2
    nsv6133704copy number variation1nstd213human GRCh37 chr19: 45,030,000-55,230,001 , GRCh38.p12 chr19: 44,525,967-54,071,460 AP2A1, APOC1, 582 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
    nsv5531321copy number variation1nstd206human GRCh38 chr19: 44,946,948-44,947,865 , GRCh37.p13 chr19: 45,450,205-45,451,122 APOC4-APOC2, APOC2
    nsv5024709copy number variation1nstd200human GRCh38 chr19: 44,901,622-44,953,076 , GRCh37.p13 chr19: 45,404,879-45,456,333 APOC1, APOC2, 6 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
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