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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7008416copy number variation1nstd229human GRCh38 chr19: 44,737,134-44,837,738 , GRCh37.p13 chr19: 45,240,391-45,340,995 CBLC, BCAM, 2 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
    nsv6528980copy number variation1nstd223human GRCh38 chr19: 44,736,936-44,741,987 , GRCh37.p13 chr19: 45,240,193-45,245,244 BCL3
    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
    nsv6522061copy number variation1nstd223human GRCh38 chr19: 44,737,134-44,837,738 , GRCh37.p13 chr19: 45,240,391-45,340,995 MIR8085, CBLC, 2 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
    nsv6218552copy number variation1nstd214human GRCh38 chr19: 44,745,986-44,746,163 , GRCh37.p13 chr19: 45,249,243-45,249,420 BCL3
    nsv6210871copy number variation1nstd214human GRCh38 chr19: 44,759,155-44,759,332 , GRCh37.p13 chr19: 45,262,412-45,262,589 BCL3, MIR8085
    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
    nsv6102937insertion1nstd212human GRCh38 chr19: 44,758,958-44,758,958 , GRCh37.p13 chr19: 45,262,215-45,262,215 MIR8085, BCL3
    nsv5659538insertion1nstd207human GRCh38 chr19: 44,751,439-44,751,439 , GRCh37.p13 chr19: 45,254,696-45,254,696 BCL3
    nsv5656644insertion1nstd207human GRCh38 chr19: 44,756,583-44,756,583 , GRCh37.p13 chr19: 45,259,840-45,259,840 BCL3
    nsv4727926copy number variation3nstd197human GRCh38.p12 chr19: 44,758,725-44,778,284 , GRCh37 chr19: 45,261,982-45,281,541 BCL3, CBLC, 1 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
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