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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7059793inversion1nstd229human GRCh38 chr19: 36,784,643-37,649,443 , GRCh37.p13 chr19: 37,275,545-38,140,344 ZNF790-AS1, ZNF829, 24 more genes
    nsv7013628copy number variation1nstd229human GRCh38 chr19: 36,945,425-37,379,636 , GRCh37.p13 chr19: 37,436,327-37,870,538 ZNF585B, ZNF875, 8 more genes
    nsv7013567copy number variation1nstd229human GRCh38 chr19: 37,169,779-37,169,975 , GRCh37.p13 chr19: 37,660,681-37,660,877 ZNF585A
    nsv7011026copy number variation1nstd229human GRCh38 chr19: 37,151,493-37,159,368 , GRCh37.p13 chr19: 37,642,395-37,650,270 ZNF585A
    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
    nsv7007937copy number variation1nstd229human GRCh38 chr19: 37,143,729-37,165,481 , GRCh37.p13 chr19: 37,634,631-37,656,383 ZNF585A
    nsv7006209copy number variation1nstd229human GRCh38 chr19: 37,166,667-37,166,706 , GRCh37.p13 chr19: 37,657,569-37,657,608 ZNF585A
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7004321copy number variation1nstd229human GRCh38 chr19: 37,143,350-37,149,901 , GRCh37.p13 chr19: 37,634,252-37,640,803 ZNF585A
    nsv7001840copy number variation1nstd229human GRCh38 chr19: 37,160,301-37,172,800 , GRCh37.p13 chr19: 37,651,203-37,663,702 ZNF585A
    nsv6999946copy number variation1nstd229human GRCh38 chr19: 37,127,823-37,159,165 , GRCh37.p13 chr19: 37,618,725-37,650,067 ZNF420, ZNF585A
    nsv6637740copy number variation1nstd102humanUncertain significance GRCh37 chr19: 37,389,799-38,562,489 , GRCh38.p12 chr19: 36,898,897-38,071,849 MTND5P45, ZNF568, 36 more genes
    nsv6624711copy number variation1nstd224human GRCh37 chr19: 37,613,594-37,988,445 , GRCh38.p12 chr19: 37,122,692-37,497,543 ZNF527, ZNF585B, 9 more genes
    nsv6597372inversion1nstd223human GRCh38 chr19: 36,322,830-37,322,723 , GRCh37.p13 chr19: 36,813,732-37,813,625 ZNF790, RPL31P61, 28 more genes
    nsv6535180copy number variation1nstd223human GRCh38 chr19: 36,416,491-37,213,522 , GRCh37.p13 chr19: 36,907,393-37,704,424 LOC644189, ZNF566-AS1, 22 more genes
    nsv6532164copy number variation1nstd223human GRCh38 chr19: 36,793,725-37,314,426 , GRCh37.p13 chr19: 37,284,627-37,805,328 ZNF829, LINC01535, 12 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6102512inversion1nstd212human GRCh38 chr19: 37,166,326-37,223,509 , GRCh37.p13 chr19: 37,657,228-37,714,411 ZNF585B, ZNF383, 1 more genes
    nsv6048006copy number variation1nstd212human GRCh38 chr19: 37,144,483-37,144,537 , GRCh37.p13 chr19: 37,635,385-37,635,439 ZNF585A
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