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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5946838copy number variation1nstd209human GRCh38 chr19: 21,972,932-22,180,934 , GRCh37.p13 chr19: 22,155,734-22,363,736 ZNF257, ZNF92P2, 8 more genes
    nsv5944165copy number variation1nstd209human GRCh38 chr19: 21,973,520-22,180,934 , GRCh37.p13 chr19: 22,156,322-22,363,736 BNIP3P29, BNIP3P28, 8 more genes
    nsv5942957copy number variation1nstd209human GRCh38 chr19: 21,595,458-22,435,310 , GRCh37.p13 chr19: 21,778,260-22,618,112 , LOC105372324, 32 more genes
    nsv5940544copy number variation1nstd209human GRCh38 chr19: 21,933,481-22,933,189 , GRCh37.p13 chr19: 22,116,283-23,115,991 , BNIP3P33, 42 more genes
    nsv5939524copy number variation1nstd209human GRCh38 chr19: 21,932,270-22,932,025 , GRCh37.p13 chr19: 22,115,072-23,114,827 , ZNF676, 42 more genes
    nsv5938160copy number variation1nstd209human GRCh38 chr19: 21,972,979-22,180,645 , GRCh37.p13 chr19: 22,155,781-22,363,447 LOC112268248, ZNF92P2, 8 more genes
    nsv5931559copy number variation1nstd209human GRCh38 chr19: 22,066,963-22,171,534 , GRCh37.p13 chr19: 22,249,765-22,354,336 ZNF257, PCGF7P, 2 more genes
    nsv5530867copy number variation1nstd206human GRCh38 chr19: 22,129,272-22,131,328 , GRCh37.p13 chr19: 22,312,074-22,314,130 ZNF92P2
    nsv5526651copy number variation1nstd206human GRCh38 chr19: 21,859,999-22,962,000 , GRCh37.p13 chr19: 22,042,801-23,144,802 , RAD54L2P1, 45 more genes
    nsv5516622copy number variation1nstd206human GRCh38 chr19: 22,066,963-22,171,535 , GRCh37.p13 chr19: 22,249,765-22,354,337 ZNF257, MTDHP5, 2 more genes
    nsv5359612translocation1nstd200human GRCh38 chr19: 22,129,272-22,129,272 , GRCh38 chr19: 22,131,328-22,131,328 , GRCh37.p13 chr19: 22,312,074-22,312,074 , GRCh37.p13 chr19: 22,314,130-22,314,130 ZNF92P2
    nsv5322156copy number variation1nstd204human GRCh37.p13 chr19: 22,249,742-22,354,366 , GRCh38.p13 chr19: 22,066,940-22,171,564 ZNF257, PCGF7P, 2 more genes
    nsv5019677copy number variation1nstd200human GRCh38 chr19: 22,066,963-22,171,535 , GRCh37.p13 chr19: 22,249,765-22,354,337 PCGF7P, ZNF92P2, 2 more genes
    nsv5019675copy number variation1nstd200human GRCh38 chr19: 22,056,717-22,371,165 , GRCh37.p13 chr19: 22,239,519-22,553,967 , ZNF92P2, 12 more genes
    nsv5019671copy number variation1nstd200human GRCh38 chr19: 22,023,376-22,303,272 , GRCh37.p13 chr19: 22,206,178-22,486,074 , MTDHP5, 11 more genes
    nsv4860813copy number variation1nstd200human GRCh37 chr19: 22,312,074-22,314,130 , GRCh38.p12 chr19|NW_003315965.1: 177,546-179,602 , GRCh38.p12 chr19: 22,129,272-22,131,328 ZNF92P2
    nsv4860811copy number variation1nstd200human GRCh37 chr19: 22,249,765-22,354,337 , GRCh38.p12 chr19: 22,066,963-22,171,535 ZNF92P2, PCGF7P, 2 more genes
    nsv4860809copy number variation1nstd200human GRCh37 chr19: 22,206,178-22,486,074 , GRCh38.p12 chr19: 22,023,376-22,303,272 , GRCh38.p12 chr19|NW_003315965.1: 1-188,024 , PCGF7P, 11 more genes
    nsv4676333copy number variation1nstd102humanLikely benign GRCh37 chr19: 22,208,751-23,199,700 , GRCh38.p12 chr19: 22,025,949-23,016,898 ZNF209P, ZNF257, 40 more genes
    nsv4676309copy number variation1nstd102humanLikely benign GRCh37 chr19: 21,717,186-23,008,275 , GRCh38.p12 chr19: 21,534,384-22,825,473 VN1R87P, LOC105372331, 51 more genes
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