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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7143108copy number variation1nstd232human GRCh37.p13 chr15: 90,051,766-90,051,822 , GRCh38.p12 chr15: 89,508,535-89,508,591 LINC00928
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv7094312copy number variation2nstd102humanUncertain significance GRCh37 chr15: 89,379,429-91,565,479 , GRCh38.p12 chr15: 88,836,198-91,022,249 IQGAP1, WDR93, 77 more genes
    nsv7076849inversion1nstd229human GRCh38 chr15: 89,041,443-89,639,935 , GRCh37.p13 chr15: 89,584,674-90,183,166 LINC00928, HMGB1P8, 17 more genes
    nsv7068128inversion1nstd229human GRCh38 chr15: 87,287,023-90,484,635 , GRCh37.p13 chr15: 87,830,254-91,027,867 , LOC105370964, 81 more genes
    nsv7065612inversion1nstd229human GRCh38 chr15: 89,041,442-91,616,740 , GRCh37.p13 chr15: 89,584,673-92,159,970 ZNF774, CRAT37, 77 more genes
    nsv7062993inversion1nstd229human GRCh38 chr15: 85,570,479-90,463,746 , GRCh37.p13 chr15: 86,113,710-91,006,978 , NTRK3-AS1, 97 more genes
    nsv6976510copy number variation1nstd229human GRCh38 chr15: 86,730,503-91,149,191 , GRCh37.p13 chr15: 87,273,734-91,692,421 , IQGAP1, 105 more genes
    nsv6976120copy number variation1nstd229human GRCh38 chr15: 89,485,595-89,519,294 , GRCh37.p13 chr15: 90,028,826-90,062,525 LINC00928, RHCG
    nsv6968297copy number variation1nstd229human GRCh38 chr15: 89,516,141-89,518,549 , GRCh37.p13 chr15: 90,059,372-90,061,780 LINC00928
    nsv6965025copy number variation1nstd229human GRCh38 chr15: 89,510,737-89,514,563 , GRCh37.p13 chr15: 90,053,968-90,057,794 LINC00928
    nsv6963886copy number variation1nstd229human GRCh38 chr15: 89,459,487-89,548,320 , GRCh37.p13 chr15: 90,002,718-90,091,551 LOC112268153, LOC105370964, 2 more genes
    nsv6958886copy number variation1nstd229human GRCh38 chr15: 89,522,917-89,528,456 , GRCh37.p13 chr15: 90,066,148-90,071,687 LINC00928
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6582041inversion1nstd223human GRCh38 chr15: 85,570,476-90,463,749 , GRCh37.p13 chr15: 86,113,707-91,006,981 , AP3S2, 97 more genes
    nsv6515309copy number variation1nstd223human GRCh38 chr15: 89,516,141-89,518,531 , GRCh37.p13 chr15: 90,059,372-90,061,762 LINC00928
    nsv6514959copy number variation1nstd223human GRCh38 chr15: 89,517,732-89,518,899 , GRCh37.p13 chr15: 90,060,963-90,062,130 LINC00928
    nsv6495952copy number variation1nstd223human GRCh38 chr15: 89,518,560-89,520,950 , GRCh37.p13 chr15: 90,061,791-90,064,181 LINC00928
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