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Items: 1 to 20 of 183

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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
    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
    nsv6971047copy number variation1nstd229human GRCh38 chr15: 89,378,601-89,380,000 , GRCh37.p13 chr15: 89,921,832-89,923,231 LOC107984777, MIR9-3HG
    nsv6969444copy number variation1nstd229human GRCh38 chr15: 89,377,591-89,377,633 , GRCh37.p13 chr15: 89,920,822-89,920,864 LOC107984777, MIR9-3HG
    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
    nsv6506317copy number variation1nstd223human GRCh38 chr15: 89,360,120-89,361,834 , GRCh37.p13 chr15: 89,903,351-89,905,065 MIR9-3HG
    nsv6309831copy number variation1nstd102humanUncertain significance GRCh37 chr15: 89,859,982-90,294,462 , GRCh38.p12 chr15: 89,316,751-89,751,231 LOC107984777, PLIN1, 19 more genes
    nsv6291795copy number variation1nstd102humanPathogenic GRCh37 chr15: 89,520,451-93,926,491 , GRCh38.p12 chr15: 88,977,220-93,383,262 LINC00930, TRY-GTA12-1, 106 more genes
    nsv6290316copy number variation1nstd102humanPathogenic GRCh37 chr15: 88,465,861-94,411,846 , GRCh38.p12 chr15: 87,922,630-93,868,617 LOC105370964, MRPL46, 130 more genes
    nsv6204521copy number variation1nstd214human GRCh38 chr15: 89,376,250-89,376,300 , GRCh37.p13 chr15: 89,919,481-89,919,531 MIR9-3HG, LOC107984777
    nsv6193530copy number variation1nstd214human GRCh38 chr15: 89,376,246-89,376,300 , GRCh37.p13 chr15: 89,919,477-89,919,531 LOC107984777, MIR9-3HG
    nsv6133155copy number variation1nstd213human GRCh37 chr15: 72,730,000-102,440,001 , GRCh38.p12 chr15: 72,437,659-101,899,798 , BLM, 609 more genes
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