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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112814copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 90,220,676-90,220,734 , GRCh38.p12 chr15: 89,677,445-89,677,503 PLIN1
    nsv5654991insertion1nstd207human GRCh38 chr15: 89,663,991-89,663,991 , GRCh37.p13 chr15: 90,207,222-90,207,222 PLIN1
    nsv5647215insertion1nstd207human GRCh38 chr15: 89,663,690-89,663,690 , GRCh37.p13 chr15: 90,206,921-90,206,921 PLIN1
    nsv5645417insertion1nstd207human GRCh38 chr15: 89,663,571-89,663,571 , GRCh37.p13 chr15: 90,206,802-90,206,802 PLIN1, KIF7
    nsv5586724copy number variation1nstd207human GRCh38 chr15: 89,663,551-89,663,630 , GRCh37.p13 chr15: 90,206,782-90,206,861 PLIN1, KIF7
    nsv5585751copy number variation1nstd207human GRCh38 chr15: 89,663,851-89,663,910 , GRCh37.p13 chr15: 90,207,082-90,207,141 PLIN1
    nsv5533115copy number variation1nstd206human GRCh38 chr15: 89,676,194-89,678,013 , GRCh37.p13 chr15: 90,219,425-90,221,244 PLIN1
    nsv5516524copy number variation1nstd206human GRCh38 chr15: 89,676,481-89,694,437 , GRCh37.p13 chr15: 90,219,712-90,237,668 WDR93, RPL36AP43, 2 more genes
    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
    nsv5009157copy number variation1nstd200human GRCh38 chr15: 89,676,492-89,780,325 , GRCh37.p13 chr15: 90,219,723-90,323,556 PLIN1, PEX11A, 6 more genes
    nsv5002294copy number variation1nstd200human GRCh38 chr15: 89,676,543-89,694,441 , GRCh37.p13 chr15: 90,219,774-90,237,672 RPL36AP43, PEX11A, 2 more genes
    nsv5002293copy number variation1nstd200human GRCh38 chr15: 89,664,555-89,664,811 , GRCh37.p13 chr15: 90,207,786-90,208,042 PLIN1
    nsv4856271copy number variation1nstd200human GRCh37 chr15: 90,207,786-90,208,042 , GRCh38.p12 chr15: 89,664,555-89,664,811 PLIN1
    nsv4765623insertion1nstd199human GRCh37 chr15: 90,206,811-90,206,811 , GRCh38.p12 chr15: 89,663,580-89,663,580 PLIN1, KIF7
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4679244copy number variation1nstd189human GRCh37.p13 chr15: 89,903,203-90,447,762 , GRCh38.p12 chr15: 89,359,972-89,904,530 , ANPEP, 26 more genes
    nsv4675805copy number variation1nstd102humanUncertain significance GRCh37 chr15: 90,111,672-90,671,886 , GRCh38.p12 chr15: 89,568,441-90,128,654 RNU6-132P, PEX11A, 23 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
    nsv4634132copy number variation1nstd183human GRCh37 chr15: 90,206,819-90,207,304 , GRCh38.p12 chr15: 89,663,588-89,664,073 PLIN1
    nsv4426775copy number variation1nstd174human GRCh37 chr15: 90,220,673-90,237,589 , GRCh38.p12 chr15: 89,677,442-89,694,358 WDR93, RPL36AP43, 2 more genes
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