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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077186inversion1nstd229human GRCh38 chr15: 35,051,912-40,816,689 , GRCh37.p13 chr15: 35,344,113-41,108,887 BUB1B-PAK6, LOC751603, 96 more genes
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6966436copy number variation1nstd229human GRCh38 chr15: 39,097,905-39,249,023 , GRCh37.p13 chr15: 39,390,106-39,541,224 LOC105370780, LINC02915
    nsv6963535copy number variation1nstd229human GRCh38 chr15: 39,252,384-39,252,829 , GRCh37.p13 chr15: 39,544,585-39,545,030 LINC02915
    nsv6958254copy number variation1nstd229human GRCh38 chr15: 38,713,174-39,291,246 , GRCh37.p13 chr15: 39,005,375-39,583,447 LOC105370777, LOC105370780, 4 more genes
    nsv6623110copy number variation2nstd224human GRCh37 chr15: 39,520,813-39,589,246 , GRCh38.p12 chr15: 39,228,612-39,297,045 LINC02915
    nsv6508648copy number variation1nstd223human GRCh38 chr15: 39,252,901-39,254,700 , GRCh37.p13 chr15: 39,545,102-39,546,901 LINC02915
    nsv6507135copy number variation1nstd223human GRCh38 chr15: 39,250,178-39,250,622 , GRCh37.p13 chr15: 39,542,379-39,542,823 LINC02915
    nsv6315190copy number variation1nstd102humanPathogenic GRCh37 chr15: 33,809,650-40,027,263 , GRCh38.p12 chr15: 33,517,449-39,735,062 RYR3, RPL32P2, 84 more genes
    nsv6132806copy number variation1nstd213human GRCh37 chr15: 39,170,000-42,090,001 , GRCh38.p12 chr15: 38,877,799-41,797,803 GCHFR, LTK, 84 more genes
    nsv6037753copy number variation1nstd212human GRCh38 chr15: 39,221,769-39,298,075 , GRCh37.p13 chr15: 39,513,970-39,590,276 LINC02915
    nsv5939106copy number variation1nstd209human GRCh38 chr15: 38,008,106-40,186,655 , GRCh37.p13 chr15: 38,300,307-40,478,856 , LOC105370784, 36 more genes
    nsv5506609copy number variation1nstd206human GRCh38 chr15: 39,250,489-39,250,558 , GRCh37.p13 chr15: 39,542,690-39,542,759 LINC02915
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv4855793copy number variation1nstd200human GRCh37 chr15: 34,109,797-39,904,401 , GRCh38.p12 chr15: 33,817,596-39,612,200 , AQR, 87 more genes
    nsv4729292copy number variation1nstd102humanUncertain significance GRCh37 chr15: 38,632,117-39,790,989 , GRCh38.p12 chr15: 38,339,916-39,498,788 LOC102724253, FAM98B, 12 more genes
    nsv4436396complex substitution1nstd102humanPathogenic GRCh38.p12 chr15: 34,346,036-41,764,885 , GRCh37 chr15: 34,638,237-42,057,083 ACTC1, BUB1B, 150 more genes
    nsv4249258copy number variation1nstd166human GRCh37.p13 chr15: 39,546,966-39,547,026 , GRCh38.p12 chr15: 39,254,765-39,254,825 LINC02915
    nsv4245248copy number variation1nstd166human GRCh37.p13 chr15: 39,005,375-39,583,447 , GRCh38.p12 chr15: 38,713,174-39,291,246 LINC02915, LOC102724253, 4 more genes
    nsv4242708copy number variation1nstd166human GRCh37.p13 chr15: 39,541,209-39,545,142 , GRCh38.p12 chr15: 39,249,008-39,252,941 LINC02915
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