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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095478copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407 NFKBID, LRP3, 141 more genes
    nsv7095275copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,439,152-33,457,392 , GRCh38.p12 chr19: 32,948,246-32,966,486 CEP89, RPL31P60
    nsv7095200copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,457,246-33,464,488 , GRCh38.p12 chr19: 32,966,340-32,973,582 FAAP24, CEP89
    nsv7077599inversion1nstd229human GRCh38 chr19: 32,882,928-32,883,663 , GRCh37.p13 chr19: 33,373,834-33,374,569 CEP89
    nsv7064982inversion1nstd229human GRCh38 chr19: 32,032,146-33,117,941 , GRCh37.p13 chr19: 32,523,052-33,608,847 LINC01782, NUDT19, 22 more genes
    nsv7009812copy number variation1nstd229human GRCh38 chr19: 32,828,507-32,907,122 , GRCh37.p13 chr19: 33,319,413-33,398,028 SLC7A9, TDRD12, 2 more genes
    nsv7008796copy number variation1nstd229human GRCh38 chr19: 32,885,050-32,892,897 , GRCh37.p13 chr19: 33,375,956-33,383,803 CEP89
    nsv7005903copy number variation1nstd229human GRCh38 chr19: 32,703,671-33,040,255 , GRCh37.p13 chr19: 33,194,577-33,531,161 SLC7A9, NUDT19, 7 more genes
    nsv7004683copy number variation1nstd229human GRCh38 chr19: 32,931,662-33,016,377 , GRCh37.p13 chr19: 33,422,568-33,507,283 RPL31P60, FAAP24, 2 more genes
    nsv7004083copy number variation1nstd229human GRCh38 chr19: 32,870,450-32,873,964 , GRCh37.p13 chr19: 33,361,356-33,364,870 SLC7A9, CEP89
    nsv6999687copy number variation1nstd229human GRCh38 chr19: 32,947,925-32,948,849 , GRCh37.p13 chr19: 33,438,831-33,439,755 CEP89
    nsv6637511copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,319,212-33,395,193 , GRCh38.p12 chr19: 32,828,306-32,904,287 TDRD12, CEP89, 2 more genes
    nsv6596670inversion1nstd223human GRCh38 chr19: 32,032,144-33,117,460 , GRCh37.p13 chr19: 32,523,050-33,608,366 DPY19L3, LINC01782, 22 more genes
    nsv6595948inversion1nstd223human GRCh38 chr19: 32,920,438-32,920,998 , GRCh37.p13 chr19: 33,411,344-33,411,904 CEP89
    nsv6535280copy number variation1nstd223human GRCh38 chr19: 32,957,604-32,958,478 , GRCh37.p13 chr19: 33,448,510-33,449,384 CEP89
    nsv6534827copy number variation1nstd223human GRCh38 chr19: 32,828,507-32,907,120 , GRCh37.p13 chr19: 33,319,413-33,398,026 TDRD12, SLC7A9, 2 more genes
    nsv6528532copy number variation1nstd223human GRCh38 chr19: 32,957,638-32,966,293 , GRCh37.p13 chr19: 33,448,544-33,457,199 CEP89, RPL31P60
    nsv6523528copy number variation1nstd223human GRCh38 chr19: 32,938,811-32,939,539 , GRCh37.p13 chr19: 33,429,717-33,430,445 CEP89
    nsv6523109copy number variation1nstd223human GRCh38 chr19: 32,918,901-32,920,800 , GRCh37.p13 chr19: 33,409,807-33,411,706 CEP89
    nsv6522984copy number variation1nstd223human GRCh38 chr19: 32,882,889-32,888,840 , GRCh37.p13 chr19: 33,373,795-33,379,746 CEP89
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