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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116455mobile element insertion1nstd186human GRCh37 chr15: 64,660,971-64,661,022 , GRCh38.p12 chr15: 64,368,772-64,368,823 PCLAF
    nsv5971229insertion1nstd209human GRCh38 chr15: 64,377,489-64,377,489 , GRCh37.p13 chr15: 64,669,688-64,669,688 PCLAF
    nsv5940756copy number variation1nstd209human GRCh38 chr15: 64,371,908-64,372,026 , GRCh37.p13 chr15: 64,664,107-64,664,225 PCLAF
    nsv5705509mobile element insertion1nstd211human GRCh38 chr15: 64,370,856-64,370,856 , GRCh37.p13 chr15: 64,663,055-64,663,055 PCLAF
    nsv5697516mobile element insertion1nstd211human GRCh38 chr15: 64,370,853-64,370,853 , GRCh37.p13 chr15: 64,663,052-64,663,052 PCLAF
    nsv5697172mobile element insertion1nstd211human GRCh38 chr15: 64,368,772-64,368,772 , GRCh37.p13 chr15: 64,660,971-64,660,971 PCLAF
    nsv5651256insertion1nstd207human GRCh38 chr15: 64,368,762-64,368,762 , GRCh37.p13 chr15: 64,660,961-64,660,961 PCLAF
    nsv5596643copy number variation1nstd207human GRCh38 chr15: 64,371,908-64,372,026 , GRCh37.p13 chr15: 64,664,107-64,664,225 PCLAF
    nsv5533548copy number variation1nstd206human GRCh38 chr15: 64,371,203-64,371,876 , GRCh37.p13 chr15: 64,663,402-64,664,075 PCLAF
    nsv5526992copy number variation1nstd206human GRCh38 chr15: 64,371,929-64,372,027 , GRCh37.p13 chr15: 64,664,128-64,664,226 PCLAF
    nsv5520160copy number variation1nstd206human GRCh38 chr15: 64,382,104-64,382,601 , GRCh37.p13 chr15: 64,674,303-64,674,800 PCLAF
    nsv5519016copy number variation1nstd206human GRCh38 chr15: 64,382,822-64,384,612 , GRCh37.p13 chr15: 64,675,021-64,676,811 PCLAF
    nsv5424264mobile element insertion1nstd206human GRCh38 chr15: 64,368,772-64,368,823 , GRCh37.p13 chr15: 64,660,971-64,661,022 PCLAF
    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
    nsv5306029copy number variation1nstd204human GRCh38.p13 chr15: 64,359,874-64,364,378 , GRCh37.p13 chr15: 64,652,073-64,656,577 PCLAF
    nsv5278079copy number variation1nstd204human GRCh38.p13 chr15: 64,359,901-64,364,400 , GRCh37.p13 chr15: 64,652,100-64,656,599 PCLAF
    nsv5267116copy number variation1nstd204human GRCh38.p13 chr15: 64,359,936-64,364,135 , GRCh37.p13 chr15: 64,652,135-64,656,334 PCLAF
    nsv5260923copy number variation1nstd204human GRCh37.p13 chr15: 64,569,600-64,876,599 , GRCh38.p13 chr15: 64,277,401-64,584,400 , TRIP4, 5 more genes
    nsv5157702mobile element insertion1nstd203human GRCh38 chr15: 64,370,788-64,370,805 , GRCh37.p13 chr15: 64,662,987-64,663,004 PCLAF
    nsv5157082mobile element insertion1nstd203human GRCh38 chr15: 64,366,384-64,366,396 , GRCh37.p13 chr15: 64,658,583-64,658,595 PCLAF
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