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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148096copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,854,238-32,892,694 , GRCh38.p12 chr15: 30,562,035-32,600,493 MTMR10, GOLGA8Q, 50 more genes
    nsv7094465copy number variation1nstd102humanUncertain significance GRCh37 chr15: 31,196,867-34,112,028 , GRCh38.p12 chr15: 30,904,664-33,819,827 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-5,161,414 , GRCh38.p12 chr15|NW_011332701.1: 3,077,944-4,998,962 RNU6-18P, CHRNA7, 72 more genes
    nsv7094281copy number variation1nstd102humanUncertain significance GRCh37 chr15: 32,393,486-34,030,811 , GRCh38.p12 chr15: 32,101,283-33,738,610 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-5,161,414 ARHGAP11B, TMCO5B, 72 more genes
    nsv7061220inversion1nstd229human GRCh38 chr15: 28,848,197-32,920,244 , GRCh37.p13 chr15: 29,093,343-33,212,445 LOC105376704, WHAMMP1, 96 more genes
    nsv6969948copy number variation1nstd229human GRCh38 chr15: 32,139,827-34,373,967 , GRCh37.p13 chr15: 32,432,028-34,666,168 AVEN, LPCAT4, 50 more genes
    nsv6637281copy number variation1nstd102humanUncertain significance GRCh37 chr15: 31,073,669-32,915,593 , GRCh38.p12 chr15: 30,781,466-32,623,392 , GRCh38.p12 chr15|NW_011332701.1: 2,954,719-4,675,523 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-4,837,975 LOC100289543, LOC644110, 58 more genes
    nsv6635794copy number variation1nstd227human GRCh38.p12 chr15: 31,762,463-32,640,449 , GRCh37 chr15: 32,054,666-32,932,650 , GRCh38.p12 chr15|NW_011332701.1: 3,935,098-4,692,581 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-4,855,033 CHRNA7, TRPM1, 59 more genes
    nsv6635028copy number variation1nstd227human GRCh38.p12 chr15: 31,727,716-32,641,286 , GRCh37 chr15: 32,019,919-32,933,487 , GRCh38.p12 chr15|NW_011332701.1: 3,900,401-4,693,418 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-4,855,870 CHRNA7, TRPM1, 59 more genes
    nsv6623103copy number variation1nstd224human GRCh37 chr15: 32,025,034-32,927,476 , GRCh38.p12 chr15: 31,732,831-32,635,275 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-4,849,859 , GRCh38.p12 chr15|NW_011332701.1: 3,905,516-4,687,407 ARHGAP11A, HERC2P10, 58 more genes
    nsv6623073copy number variation1nstd224human GRCh37 chr15: 32,049,125-32,908,419 , GRCh38.p12 chr15: 31,756,922-32,616,218 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-4,830,798 , GRCh38.p12 chr15|NW_011332701.1: 3,929,572-4,668,346 KLF13, ARHGAP11B, 58 more genes
    nsv6508470copy number variation1nstd223human GRCh38 chr15: 32,520,601-32,524,100 , GRCh37.p13 chr15: 32,812,802-32,816,301 WHAMMP1
    nsv6504389copy number variation1nstd223human GRCh38 chr15: 30,639,774-32,629,847 , GRCh37.p13 chr15: 30,931,977-32,922,048 LOC112268159, DNM1P32, 46 more genes
    nsv6497910copy number variation1nstd223human GRCh38 chr15: 32,521,801-32,522,800 , GRCh37.p13 chr15: 32,814,002-32,815,001 WHAMMP1
    nsv6497505copy number variation1nstd223human GRCh38 chr15: 32,139,826-34,373,966 , GRCh37.p13 chr15: 32,432,027-34,666,167 TMCO5B, LPCAT4, 50 more genes
    nsv6497272copy number variation1nstd223human GRCh38 chr15: 32,517,901-32,522,800 , GRCh37.p13 chr15: 32,810,102-32,815,001 WHAMMP1
    nsv6315516copy number variation1nstd102humanPathogenic GRCh37 chr15: 31,098,690-32,914,240 , GRCh38.p12 chr15: 30,806,487-32,622,039 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-4,836,622 , GRCh38.p12 chr15|NW_011332701.1: 2,979,743-4,674,170 LOC100289543, LOC644110, 58 more genes
    nsv6314962copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,783,603-32,914,393 , GRCh38.p12 chr15: 30,491,400-32,622,192 ULK4P2, ULK4P1, 54 more genes
    nsv6305852copy number variation1nstd186human GRCh37 chr15: 32,804,419-32,810,388 , GRCh38.p12 chr15: 32,512,218-32,518,187 , WHAMMP1
    nsv6145353copy number variation1nstd206human GRCh38 chr15: 32,512,218-32,518,187 , GRCh37.p13 chr15: 32,804,419-32,810,388 , WHAMMP1
    nsv6145183copy number variation1nstd206human GRCh38 chr15: 32,531,874-32,576,874 , GRCh37.p13 chr15: 32,824,075-32,869,075 WHAMMP1, LINC02256
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