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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
    nsv7017756copy number variation1nstd229human GRCh38 chr19: 37,548,077-37,822,264 , GRCh37.p13 chr19: 38,038,979-38,312,904 MTND5P45, LOC728533, 14 more genes
    nsv7017479copy number variation1nstd229human GRCh38 chr19: 37,564,459-37,564,562 , GRCh37.p13 chr19: 38,055,361-38,055,464 ZNF571-AS1, ZNF571, 1 more genes
    nsv7016336copy number variation1nstd229human GRCh38 chr19: 37,572,667-37,665,120 , GRCh37.p13 chr19: 38,063,569-38,156,021 ZNF571-AS1, MTCO1P41, 4 more genes
    nsv7014727copy number variation1nstd229human GRCh38 chr19: 37,571,795-38,134,006 , GRCh37.p13 chr19: 38,062,697-38,624,646 LOC105372395, ZNF573, 19 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
    nsv7006264copy number variation1nstd229human GRCh38 chr19: 37,587,701-37,590,600 , GRCh37.p13 chr19: 38,078,602-38,081,501 ZNF571-AS1, ZNF571, 1 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
    nsv7005099copy number variation1nstd229human GRCh38 chr19: 37,522,527-37,618,407 , GRCh37.p13 chr19: 38,013,429-38,109,308 ZNF571, ZNF571-AS1, 5 more genes
    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
    nsv6528478copy number variation1nstd223human GRCh38 chr19: 37,564,701-37,567,500 , GRCh37.p13 chr19: 38,055,603-38,058,402 ZNF571-AS1, ZNF571, 1 more genes
    nsv6522639copy number variation1nstd223human GRCh38 chr19: 37,522,517-37,618,370 , GRCh37.p13 chr19: 38,013,419-38,109,271 ZNF540, ZNF793, 5 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
    nsv6251030mobile element insertion1nstd215human GRCh38 chr19: 37,566,401-37,566,401 , GRCh37.p13 chr19: 38,057,303-38,057,303 ZNF571, ZNF540, 1 more genes
    nsv6211513copy number variation1nstd214human GRCh38 chr19: 37,563,751-37,563,818 , GRCh37.p13 chr19: 38,054,653-38,054,720 ZNF571, ZNF540, 1 more genes
    nsv6210237copy number variation1nstd214human GRCh38 chr19: 37,563,615-37,563,682 , GRCh37.p13 chr19: 38,054,517-38,054,584 ZNF571, ZNF540, 1 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
    nsv6104162insertion1nstd212human GRCh38 chr19: 37,587,809-37,587,809 , GRCh37.p13 chr19: 38,078,710-38,078,710 ZNF571, ZNF540, 1 more genes
    nsv6046361copy number variation1nstd212human GRCh38 chr19: 37,563,759-37,563,824 , GRCh37.p13 chr19: 38,054,661-38,054,726 ZNF571, ZNF540, 1 more genes
    nsv5943607copy number variation1nstd209human GRCh38 chr19: 37,565,056-37,565,139 , GRCh37.p13 chr19: 38,055,958-38,056,041 ZNF571, ZNF540, 1 more genes
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