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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
    nsv7058395inversion1nstd229human GRCh38 chr19: 37,249,810-37,253,184 , GRCh37.p13 chr19: 37,740,712-37,744,086 LINC01535
    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
    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
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7001764copy number variation1nstd229human GRCh38 chr19: 37,245,031-37,257,552 , GRCh37.p13 chr19: 37,735,933-37,748,454 LINC01535, ZNF383
    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
    nsv6596070inversion1nstd223human GRCh38 chr19: 37,252,998-37,253,474 , GRCh37.p13 chr19: 37,743,900-37,744,376 LINC01535
    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
    nsv6532013copy number variation1nstd223human GRCh38 chr19: 37,254,374-37,255,601 , GRCh37.p13 chr19: 37,745,276-37,746,503 LINC01535
    nsv6522008copy number variation1nstd223human GRCh38 chr19: 37,245,220-37,257,687 , GRCh37.p13 chr19: 37,736,122-37,748,589 ZNF383, LINC01535
    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
    nsv6287103insertion1nstd214human GRCh38 chr19: 37,251,771-37,251,771 , GRCh37.p13 chr19: 37,742,673-37,742,673 LINC01535
    nsv6235684insertion4nstd214human GRCh38 chr19: 37,251,761-37,251,761 , GRCh37.p13 chr19: 37,742,663-37,742,663 LINC01535
    nsv6145399copy number variation1nstd206human GRCh38 chr19: 37,262,874-37,268,874 , GRCh37.p13 chr19: 37,753,776-37,759,776 LINC01535, LOC284412
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6129308insertion1nstd186human GRCh37 chr19: 37,742,680-37,742,683 , GRCh38.p12 chr19: 37,251,778-37,251,781 LINC01535
    nsv6109830insertion1nstd212human GRCh38 chr19: 37,251,761-37,251,761 , GRCh37.p13 chr19: 37,742,663-37,742,663 LINC01535
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