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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
    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
    nsv6970046copy number variation1nstd229human GRCh38 chr15: 92,740,860-93,077,278 , GRCh37.p13 chr15: 93,284,090-93,620,507 CHASERR, MIR3175, 6 more genes
    nsv6964440copy number variation1nstd229human GRCh38 chr15: 92,898,610-92,898,720 , GRCh37.p13 chr15: 93,441,840-93,441,950 CHASERR, CHD2
    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
    nsv6623356copy number variation1nstd224human GRCh37 chr15: 93,307,668-93,510,603 , GRCh38.p12 chr15: 92,764,438-92,967,373 CHASERR, LOC101926994, 3 more genes
    nsv6578792inversion1nstd223human GRCh38 chr15: 92,893,975-92,894,693 , GRCh37.p13 chr15: 93,437,205-93,437,923 CHASERR
    nsv6512942copy number variation1nstd223human GRCh38 chr15: 92,882,101-92,883,400 , GRCh37.p13 chr15: 93,425,331-93,426,630 CHASERR
    nsv6508686copy number variation1nstd223human GRCh38 chr15: 92,896,001-92,896,500 , GRCh37.p13 chr15: 93,439,231-93,439,730 CHASERR
    nsv6507123copy number variation1nstd223human GRCh38 chr15: 92,751,042-93,010,689 , GRCh37.p13 chr15: 93,294,272-93,553,919 MIR3175, CHD2, 4 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
    nsv6133155copy number variation1nstd213human GRCh37 chr15: 72,730,000-102,440,001 , GRCh38.p12 chr15: 72,437,659-101,899,798 , BLM, 609 more genes
    nsv6132919copy number variation1nstd213human GRCh37 chr15: 91,580,000-100,660,001 , GRCh38.p12 chr15: 91,036,770-100,119,796 ST8SIA2, SYNM, 116 more genes
    nsv6132917copy number variation1nstd213human GRCh37 chr15: 90,230,000-95,470,001 , GRCh38.p12 chr15: 89,686,769-94,926,772 BLM, ST8SIA2, 101 more genes
    nsv6112780copy number variation1nstd102humanPathogenic GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538 LOC105371009, ST8SIA2, 149 more genes
    nsv5694681mobile element insertion2nstd211human GRCh38 chr15: 92,881,576-92,881,576 , GRCh37.p13 chr15: 93,424,806-93,424,806 CHASERR
    nsv5531067copy number variation1nstd206human GRCh38 chr15: 92,402,520-97,547,707 , GRCh37.p13 chr15: 92,945,750-98,090,937 , LOC105371004, 71 more genes
    nsv5419274mobile element insertion1nstd206human GRCh38 chr15: 92,881,576-92,881,627 , GRCh37.p13 chr15: 93,424,806-93,424,857 CHASERR
    nsv5272015copy number variation1nstd204human GRCh38.p13 chr15: 92,883,601-92,941,000 , GRCh37.p13 chr15: 93,426,831-93,484,230 MIR3175, CHASERR, 1 more genes
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