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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5860131copy number variation1nstd209human GRCh38 chr15: 32,614,104-32,620,847 , GRCh37.p13 chr15: 32,906,305-32,913,048 ARHGAP11A-SCG5, ARHGAP11A-DT, 1 more genes
    nsv5856445copy number variation2nstd209human GRCh38 chr15: 32,612,728-32,615,041 , GRCh37.p13 chr15: 32,904,929-32,907,242 ARHGAP11A, ARHGAP11A-DT, 1 more genes
    nsv5700322mobile element insertion1nstd211human GRCh38 chr15: 32,586,128-32,586,128 , GRCh37.p13 chr15: 32,878,329-32,878,329 ARHGAP11A-DT
    nsv5600593copy number variation1nstd207human GRCh38 chr15: 32,595,484-32,595,792 , GRCh37.p13 chr15: 32,887,685-32,887,993 GOLGA8N, ARHGAP11A-DT
    nsv5586173copy number variation1nstd207human GRCh38 chr15: 32,607,506-32,608,059 , GRCh37.p13 chr15: 32,899,707-32,900,260 ARHGAP11A-DT, GOLGA8N
    nsv5509623copy number variation1nstd206human GRCh38 chr15: 32,614,357-32,614,501 , GRCh37.p13 chr15: 32,906,558-32,906,702 ARHGAP11A, ARHGAP11A-SCG5, 1 more genes
    nsv5504172copy number variation1nstd206human GRCh38 chr15: 32,602,874-32,635,937 , GRCh37.p13 chr15: 32,895,075-32,928,138 ARHGAP11A-SCG5, GOLGA8N, 3 more genes
    nsv5417798mobile element insertion1nstd206human GRCh38 chr15: 32,586,078-32,586,128 , GRCh37.p13 chr15: 32,878,279-32,878,329 ARHGAP11A-DT
    nsv5277977copy number variation1nstd204human GRCh38.p13 chr15: 32,583,901-32,586,200 , GRCh37.p13 chr15: 32,876,102-32,878,401 ARHGAP11A-DT
    nsv5277070copy number variation1nstd204human GRCh38.p13 chr15: 32,580,701-32,586,900 , GRCh37.p13 chr15: 32,872,902-32,879,101 LINC02256, ARHGAP11A-DT
    nsv5275792copy number variation1nstd204human GRCh38.p13 chr15: 32,605,205-32,629,084 , GRCh37.p13 chr15: 32,897,406-32,921,285 GOLGA8N, ARHGAP11A-SCG5, 2 more genes
    nsv5274409copy number variation1nstd204human GRCh38.p13 chr15: 32,580,701-32,600,500 , GRCh37.p13 chr15: 32,872,902-32,892,701 ARHGAP11A-DT, LINC02256, 2 more genes
    nsv5271107copy number variation1nstd204human GRCh38.p13 chr15: 32,582,401-32,586,900 , GRCh37.p13 chr15: 32,874,602-32,879,101 ARHGAP11A-DT
    nsv5270094copy number variation1nstd204human GRCh38.p13 chr15: 32,584,101-32,584,700 , GRCh37.p13 chr15: 32,876,302-32,876,901 ARHGAP11A-DT
    nsv5270072copy number variation1nstd204human GRCh38.p13 chr15: 32,592,401-32,593,400 , GRCh37.p13 chr15: 32,884,602-32,885,601 ARHGAP11A-DT, GOLGA8N
    nsv5263572copy number variation1nstd204human GRCh38.p13 chr15: 32,606,417-32,663,427 , GRCh37.p13 chr15: 32,898,618-32,955,628 GOLGA8N, ARHGAP11A, 3 more genes
    nsv5260576copy number variation1nstd204human GRCh38.p13 chr15: 32,584,517-32,586,180 , GRCh37.p13 chr15: 32,876,718-32,878,381 ARHGAP11A-DT
    nsv5001134copy number variation1nstd200human GRCh38 chr15: 31,906,597-32,688,706 , GRCh37.p13 chr15: 32,198,800-32,980,907 , DNM1P32, 29 more genes
    nsv4855766copy number variation1nstd200human GRCh37 chr15: 32,198,800-32,980,907 , GRCh38.p12 chr15: 31,906,597-32,688,706 , GRCh38.p12 chr15|NT_187660.1: 2,721,314-4,903,294 , GRCh38.p12 chr15|NW_011332701.1: 4,079,283-4,740,842 , LINC02352, 68 more genes
    nsv4749247copy number variation1nstd199human GRCh37 chr15: 29,159,443-34,700,525 , GRCh38.p12 chr15: 28,914,297-34,408,324 , GRCh38.p12 chr15|NT_187660.1: 1,192,197-5,161,414 , GRCh38.p12 chr15|NW_011332701.1: 1,079,713-4,998,962 , HNRNPA1P71, 132 more genes
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