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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144178insertion1nstd232human GRCh37.p13 chr19: 6,700,708-6,700,708 , GRCh38.p12 chr19: 6,700,697-6,700,697 C3
    nsv7138623copy number variation1nstd232human GRCh37.p13 chr19: 6,718,879-6,718,929 , GRCh38.p12 chr19: 6,718,868-6,718,918 C3
    nsv7095726copy number variation1nstd102humanPathogenic GRCh37 chr19: 6,361,586-8,212,364 , GRCh38.p12 chr19: 6,361,575-8,147,480 SLC25A23, LYPLA2P2, 77 more genes
    nsv7095674copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 6,692,915-6,697,825 , GRCh38.p12 chr19: 6,692,904-6,697,814 C3
    nsv7095298copy number variation1nstd102humanPathogenic GRCh37 chr19: 6,718,085-6,720,600 , GRCh38.p12 chr19: 6,718,074-6,720,589 C3
    nsv7095227copy number variation1nstd102humanUncertain significance GRCh37 chr19: 6,681,932-6,690,758 , GRCh38.p12 chr19: 6,681,921-6,690,747 C3
    nsv7074420inversion1nstd229human GRCh38 chr19: 6,666,620-6,968,690 , GRCh37.p13 chr19: 6,666,631-6,968,701 SH2D3A, LOC105372256, 8 more genes
    nsv7071060inversion1nstd229human GRCh38 chr19: 6,551,672-6,941,173 , GRCh37.p13 chr19: 6,551,683-6,941,184 C3, LOC100421483, 11 more genes
    nsv7070187inversion1nstd229human GRCh38 chr19: 6,518,823-8,315,881 , GRCh37.p13 chr19: 6,518,834-8,380,765 , ZNF557, 69 more genes
    nsv7068649inversion1nstd229human GRCh38 chr19: 4,313,135-7,007,201 , GRCh37.p13 chr19: 4,313,132-7,007,212 CAPS, SH2D3A, 93 more genes
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7066921inversion1nstd229human GRCh38 chr19: 4,809,260-7,077,959 , GRCh37.p13 chr19: 4,809,272-7,077,970 MLLT1, GPR108, 74 more genes
    nsv7066716inversion1nstd229human GRCh38 chr19: 6,518,017-8,344,162 , GRCh37.p13 chr19: 6,518,028-8,409,046 , STXBP2, 71 more genes
    nsv7017917copy number variation1nstd229human GRCh38 chr19: 6,656,897-6,684,330 , GRCh37.p13 chr19: 6,656,908-6,684,341 TNFSF14, C3
    nsv7016481copy number variation1nstd229human GRCh38 chr19: 6,554,801-6,905,600 , GRCh37.p13 chr19: 6,554,812-6,905,611 GPR108, MIR6791, 11 more genes
    nsv7009144copy number variation1nstd229human GRCh38 chr19: 6,655,529-6,689,275 , GRCh37.p13 chr19: 6,655,540-6,689,286 TNFSF14, C3
    nsv7004456copy number variation1nstd229human GRCh38 chr19: 6,677,401-6,682,500 , GRCh37.p13 chr19: 6,677,412-6,682,511 C3
    nsv7002062copy number variation1nstd229human GRCh38 chr19: 6,594,181-6,680,700 , GRCh37.p13 chr19: 6,594,192-6,680,711 TNFSF14, RPL7P50, 1 more genes
    nsv6599224inversion1nstd223human GRCh38 chr19: 5,796,324-7,362,002 , GRCh37.p13 chr19: 5,796,335-7,426,888 C3, CAPS, 53 more genes
    nsv6598061inversion1nstd223human GRCh38 chr19: 6,551,672-6,941,175 , GRCh37.p13 chr19: 6,551,683-6,941,186 MIR6791, TRIP10, 11 more genes
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