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Items: 1 to 20 of 226

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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
    nsv7014737copy number variation1nstd229human GRCh38 chr19: 43,559,820-43,683,290 , GRCh37.p13 chr19: 44,063,972-44,187,442 RN7SL368P, PLAUR, 8 more genes
    nsv7014177copy number variation1nstd229human GRCh38 chr19: 43,651,613-43,716,473 , GRCh37.p13 chr19: 44,155,765-44,220,625 RN7SL368P, IRGC, 2 more genes
    nsv7009958copy number variation1nstd229human GRCh38 chr19: 43,660,806-43,663,134 , GRCh37.p13 chr19: 44,164,958-44,167,286 PLAUR, RN7SL368P
    nsv7009807copy number variation1nstd229human GRCh38 chr19: 43,649,144-43,652,224 , GRCh37.p13 chr19: 44,153,296-44,156,376 PLAUR
    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
    nsv6998809copy number variation1nstd229human GRCh38 chr19: 43,666,864-43,673,487 , GRCh37.p13 chr19: 44,171,016-44,177,639 PLAUR
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6598163inversion1nstd223human GRCh38 chr19: 43,647,070-43,647,674 , GRCh37.p13 chr19: 44,151,222-44,151,826 PLAUR
    nsv6534747copy number variation1nstd223human GRCh38 chr19: 43,660,803-43,663,134 , GRCh37.p13 chr19: 44,164,955-44,167,286 RN7SL368P, PLAUR
    nsv6516839copy number variation1nstd223human GRCh38 chr19: 43,652,001-43,653,800 , GRCh37.p13 chr19: 44,156,153-44,157,952 PLAUR
    nsv6251067mobile element insertion1nstd215human GRCh38 chr19: 43,648,476-43,648,476 , GRCh37.p13 chr19: 44,152,628-44,152,628 PLAUR
    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
    nsv6131629insertion1nstd186human GRCh37 chr19: 44,169,865-44,169,865 , GRCh38.p12 chr19: 43,665,713-43,665,713 PLAUR
    nsv6129904insertion1nstd186human GRCh37 chr19: 44,160,406-44,160,444 , GRCh38.p12 chr19: 43,656,254-43,656,292 PLAUR
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