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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095657copy number variation1nstd102humanUncertain significance GRCh37 chr19: 44,011,002-45,213,778 , GRCh38.p12 chr19: 43,506,850-44,710,506 RN7SL368P, ZNF112, 52 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
    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
    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
    nsv6599857inversion1nstd223human GRCh38 chr19: 44,620,000-44,620,656 , GRCh37.p13 chr19: 45,123,310-45,123,954 IGSF23
    nsv6533352copy number variation1nstd223human GRCh38 chr19: 44,585,589-44,621,254 , GRCh37.p13 chr19: 45,088,848-45,124,552 IGSF23
    nsv6526580copy number variation1nstd223human GRCh38 chr19: 44,635,862-44,636,314 , GRCh37.p13 chr19: 45,139,162-45,139,614 CEACAM16-AS1, IGSF23
    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
    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
    nsv6102453insertion1nstd212human GRCh38 chr19: 44,629,623-44,629,623 , GRCh37.p13 chr19: 45,132,921-45,132,921 IGSF23
    nsv6051497copy number variation1nstd212human GRCh38 chr19: 44,624,152-44,624,301 , GRCh37.p13 chr19: 45,127,449-45,127,598 IGSF23
    nsv5943202copy number variation1nstd209human GRCh38 chr19: 44,628,230-44,628,306 , GRCh37.p13 chr19: 45,131,528-45,131,604 IGSF23
    nsv5528613copy number variation1nstd206human GRCh38 chr19: 44,615,022-44,621,051 , GRCh37.p13 chr19: 45,118,332-45,124,349 IGSF23
    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
    nsv4623840copy number variation1nstd183human GRCh37 chr19: 45,020,272-45,216,013 , GRCh38.p12 chr19: 44,516,211-44,712,744 PVR, CEACAM19, 7 more genes
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