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Items: 1 to 20 of 123

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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
    nsv7061070inversion1nstd229human GRCh38 chr19: 43,830,632-43,949,861 , GRCh37.p13 chr19: 44,334,784-44,454,013 ZNF45, ZNF221, 3 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
    nsv7000611copy number variation1nstd229human GRCh38 chr19: 43,902,165-43,906,234 , GRCh37.p13 chr19: 44,406,317-44,410,386 LOC100505715
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6535052copy number variation1nstd223human GRCh38 chr19: 43,902,163-43,906,231 , GRCh37.p13 chr19: 44,406,315-44,410,383 LOC100505715
    nsv6520350copy number variation1nstd223human GRCh38 chr19: 43,899,693-43,900,469 , GRCh37.p13 chr19: 44,403,845-44,404,621 LOC100505715
    nsv6226404copy number variation1nstd214human GRCh38 chr19: 43,895,257-43,895,354 , GRCh37.p13 chr19: 44,399,409-44,399,506 LOC100505715
    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
    nsv5703680mobile element insertion2nstd211human GRCh38 chr19: 43,891,550-43,891,550 , GRCh37.p13 chr19: 44,395,702-44,395,702 LOC100505715
    nsv5525434copy number variation1nstd206human GRCh38 chr19: 43,895,260-43,895,355 , GRCh37.p13 chr19: 44,399,412-44,399,507 LOC100505715
    nsv5525081copy number variation1nstd206human GRCh38 chr19: 43,899,694-43,900,469 , GRCh37.p13 chr19: 44,403,846-44,404,621 LOC100505715
    nsv5524372copy number variation1nstd206human GRCh38 chr19: 43,894,671-43,894,766 , GRCh37.p13 chr19: 44,398,823-44,398,918 LOC100505715
    nsv5425800mobile element insertion1nstd206human GRCh38 chr19: 43,891,550-43,891,601 , GRCh37.p13 chr19: 44,395,702-44,395,753 LOC100505715
    nsv5179917mobile element insertion1nstd203human GRCh38 chr19: 43,893,553-43,893,564 , GRCh37.p13 chr19: 44,397,705-44,397,716 LOC100505715
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