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Items: 1 to 20 of 112

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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
    nsv7016541copy number variation1nstd229human GRCh38 chr19: 43,697,894-43,761,514 , GRCh37.p13 chr19: 44,202,046-44,265,666 SMG9, IRGC, 1 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
    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
    nsv7005406copy number variation1nstd229human GRCh38 chr19: 43,719,711-43,722,335 , GRCh37.p13 chr19: 44,223,863-44,226,487 IRGC
    nsv6999054copy number variation1nstd229human GRCh38 chr19: 43,715,650-43,716,352 , GRCh37.p13 chr19: 44,219,802-44,220,504 IRGC
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6524479copy number variation1nstd223human GRCh38 chr19: 43,707,730-43,741,488 , GRCh37.p13 chr19: 44,211,882-44,245,640 SMG9, IRGC
    nsv6521094copy number variation1nstd223human GRCh38 chr19: 43,715,554-43,716,496 , GRCh37.p13 chr19: 44,219,706-44,220,648 IRGC
    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
    nsv5526554copy number variation1nstd206human GRCh38 chr19: 43,719,050-43,731,363 , GRCh37.p13 chr19: 44,223,202-44,235,515 SMG9, IRGC
    nsv4678976copy number variation1nstd189human GRCh37.p13 chr19: 44,188,628-44,507,055 , GRCh38.p12 chr19: 43,684,476-44,002,903 KCNN4, ZNF45, 11 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
    nsv4371631copy number variation1nstd173human GRCh37 chr19: 44,133,648-44,247,651 , GRCh38.p12 chr19: 43,629,496-43,743,499 , IRGC, 6 more genes
    nsv4365671copy number variation1nstd173human GRCh37 chr19: 44,133,648-44,247,663 , GRCh38.p12 chr19: 43,629,496-43,743,511 , PLAUR, 6 more genes
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