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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146532copy number variation1nstd232human GRCh37.p13 chr19: 55,658,713-55,658,785 , GRCh38.p12 chr19: 55,147,345-55,147,417 TNNT1
    nsv7140365copy number variation1nstd232human GRCh37.p13 chr19: 55,658,669-55,658,777 , GRCh38.p12 chr19: 55,147,301-55,147,409 TNNT1
    nsv7095670copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,644,283-55,668,957 , GRCh38.p12 chr19: 55,132,915-55,157,589 DNAAF3, TNNI3, 2 more genes
    nsv7095224copy number variation1nstd102humanPathogenic GRCh37 chr19: 55,644,283-55,678,016 , GRCh38.p12 chr19: 55,132,915-55,166,648 TNNT1, DNAAF3, 2 more genes
    nsv7075760inversion1nstd229human GRCh38 chr19: 54,368,885-57,042,988 , GRCh37.p13 chr19: 55,595,687-57,554,356 ZSCAN5C, TMEM190, 137 more genes
    nsv7067331inversion1nstd229human GRCh38 chr19: 54,730,353-56,291,074 , GRCh37.p13 chr19: 55,595,687-56,802,443 NLRP2, KIR2DP1, 85 more genes
    nsv7063630inversion1nstd229human GRCh38 chr19: 54,312,295-55,433,689 , GRCh37.p13 chr19|NW_004166865.1: 286,662-1,058,686 BRSK1, VN1R104P, 69 more genes
    nsv7062087inversion1nstd229human GRCh38 chr19: 54,368,882-57,042,981 , GRCh37.p13 chr19: 55,595,687-57,554,349 BRSK1, ZIM2, 137 more genes
    nsv7060532inversion1nstd229human GRCh38 chr19: 54,888,784-55,573,986 , GRCh37.p13 chr19: 55,595,687-56,085,352 SSC5D, MIR6804, 41 more genes
    nsv7014769copy number variation1nstd229human GRCh38 chr19: 55,018,959-55,148,797 , GRCh37.p13 chr19|NW_004166865.1: 993,327-1,058,686 MIR7975, TNNT1, 5 more genes
    nsv7009769copy number variation1nstd229human GRCh38 chr19: 55,139,547-55,144,449 , GRCh37.p13 chr19: 55,650,915-55,655,817 TNNT1
    nsv7009002copy number variation1nstd229human GRCh38 chr19: 55,122,527-55,141,761 , GRCh37.p13 chr19: 55,633,895-55,653,129 TNNT1, MIR7975
    nsv7004572copy number variation1nstd229human GRCh38 chr19: 55,140,498-55,150,588 , GRCh37.p13 chr19: 55,651,866-55,661,956 TNNT1, TNNI3
    nsv7003609copy number variation1nstd229human GRCh38 chr19: 55,128,490-55,134,554 , GRCh37.p13 chr19: 55,639,858-55,645,922 TNNT1
    nsv7003530copy number variation1nstd229human GRCh38 chr19: 55,088,846-55,180,223 , GRCh37.p13 chr19: 55,600,214-55,691,591 DNAAF3-AS1, TNNT1, 6 more genes
    nsv7003373copy number variation1nstd229human GRCh38 chr19: 55,136,620-55,193,575 , GRCh37.p13 chr19: 55,647,988-55,704,943 PTPRH, TNNI3, 4 more genes
    nsv7001282copy number variation1nstd229human GRCh38 chr19: 54,937,523-55,162,404 , GRCh37.p13 chr19|NW_004166865.1: 911,891-1,058,686 TNNT1, RPL36AP50, 12 more genes
    nsv6999655copy number variation1nstd229human GRCh38 chr19: 55,138,090-55,164,348 , GRCh37.p13 chr19: 55,649,458-55,675,716 DNAAF3-AS1, TNNI3, 2 more genes
    nsv6637813copy number variation1nstd102humanUncertain significance GRCh37 chr19: 55,642,778-55,932,200 , GRCh38.p12 chr19: 55,131,410-55,420,833 TMEM150B, TNNI3, 23 more genes
    nsv6625044copy number variation1nstd224human GRCh37 chr19: 55,324,675-55,671,337 , GRCh38.p12 chr19: 54,911,986-55,159,969 , GRCh38.p12 chr19|NW_003571061.2: 609,417-796,479 , GRCh38.p12 chr19|NW_003571057.2: 904,779-1,091,841 , GRCh38.p12 chr19|NW_003571058.2: 819,634-1,066,390 , GRCh38.p12 chr19|NW_003571059.2: 763,398-1,002,683 , GRCh38.p12 chr19|NW_003571060.1: 717,585-987,100 , GRCh38.p12 chr19|NW_003571056.2: 811,616-1,064,304 , GRCh38.p12 chr19|NW_003571055.2: 431,085-729,520 , GRCh38.p12 chr19|NW_003571054.1: 800,654-987,716 , GRCh38.p12 chr19|NT_187675.1: 90,883-282,224 KIR3DS1, NLRP2, 27 more genes
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