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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5002295copy number variation1nstd200human GRCh38 chr15: 89,684,869-89,687,171 , GRCh37.p13 chr15: 90,228,100-90,230,402 PEX11A, RPL36AP43
    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
    nsv4856272copy number variation1nstd200human GRCh37 chr15: 90,228,100-90,230,402 , GRCh38.p12 chr15: 89,684,869-89,687,171 RPL36AP43, PEX11A
    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
    nsv4509867mobile element insertion1nstd166human GRCh37.p13 chr15: 90,223,332-90,223,332 , GRCh38.p12 chr15: 89,680,101-89,680,101 PEX11A
    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
    nsv4377776copy number variation1nstd173human GRCh37 chr15: 86,980,083-93,499,239 , GRCh38.p12 chr15: 86,436,852-92,956,009 , RNU6-1111P, 136 more genes
    nsv4373893copy number variation1nstd173human GRCh37 chr15: 90,226,947-90,281,381 , GRCh38.p12 chr15: 89,683,716-89,738,150 PEX11A, WDR93, 3 more genes
    nsv4350274copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,883,823-92,165,844 , GRCh38.p12 chr15: 83,215,071-91,622,614 AKAP13, LOC105370972, 184 more genes
    nsv4239633copy number variation1nstd166human GRCh37.p13 chr15: 90,220,000-90,280,400 , GRCh38.p12 chr15: 89,676,769-89,737,169 PLIN1, PEX11A, 4 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3921462copy number variation1nstd102humanUncertain significance NCBI36 chr15: 87,527,741-88,772,110 , GRCh37.p13 chr15: 89,726,737-90,971,106 , GRCh38.p12 chr15: 89,183,506-90,427,874 LOC100631255, RN7SL736P, 51 more genes
    nsv3920352copy number variation1nstd102humanPathogenic GRCh38 chr15: 83,711,377-101,843,270 , NCBI36 chr15: 82,171,133-100,200,996 , GRCh37 chr15: 84,380,129-102,383,473 LOC102724465, SNRPA1, 333 more genes
    nsv3920248copy number variation1nstd102humanPathogenic NCBI36 chr15: 87,618,716-100,262,146 , GRCh37.p13 chr15: 89,817,712-102,444,623 , GRCh38.p12 chr15: 89,274,481-101,904,420 FAM149B1P1, MIR9-3HG, 229 more genes
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