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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148137copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,805,785-32,686,484 , GRCh38.p12 chr15: 30,513,582-32,394,283 LINC02352, CHRNA7, 37 more genes
    nsv7148125copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,918,974-32,442,006 , GRCh38.p12 chr15: 30,626,771-32,149,805 KLF13, MTMR10, 21 more genes
    nsv7148118copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,897,996-32,442,006 , GRCh38.p12 chr15: 30,605,793-32,149,805 MTMR10, LOC101930434, 24 more genes
    nsv7148111copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,742,396-28,567,325 , GRCh38.p12 chr15: 23,319,714-28,322,179 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 SNORD116-18, PWAR4, 246 more genes
    nsv7148103copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,850,097-32,693,726 , GRCh38.p12 chr15: 30,557,894-32,401,525 LOC400347, GOLGA8Q, 37 more genes
    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
    nsv7137213copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-30,386,398 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-30,094,195 TVP23BP1, SNORD115-1, 247 more genes
    nsv7098888copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,888,853-32,539,607 , GRCh38.p12 chr15: 30,596,650-32,247,406 FAN1, ARHGAP11B, 26 more genes
    nsv7098883copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,406,271-28,566,579 , GRCh38.p12 chr15: 23,319,714-28,321,433 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC105370739, SNORD116-27, 246 more genes
    nsv7094528copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,906,349-32,446,187 , GRCh38.p12 chr15: 30,614,146-32,153,986 LOC101930434, HERC2P10, 23 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
    nsv7093407copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,525-28,544,662 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,299,516 UBE2CP4, SERPINE4P, 246 more genes
    nsv7072271inversion1nstd229human GRCh38 chr15: 30,736,808-31,641,826 , GRCh37.p13 chr15: 31,029,011-31,934,029 KLF13, HERC2P10, 18 more genes
    nsv7070433inversion1nstd229human GRCh38 chr15: 28,680,335-30,817,180 , GRCh37.p13 chr15: 28,925,481-31,109,383 RNU6-17P, RN7SL628P, 54 more genes
    nsv7068342inversion1nstd229human GRCh38 chr15: 29,120,877-31,530,094 , GRCh37.p13 chr15: 29,413,080-31,822,297 ULK4P2, TRPM1, 57 more genes
    nsv7065318inversion1nstd229human GRCh38 chr15: 29,942,582-32,138,315 , GRCh37.p13 chr15: 30,234,785-32,430,516 GOLGA8T, ARHGAP11B, 52 more genes
    nsv7065102inversion1nstd229human GRCh38 chr15: 30,639,088-30,652,481 , GRCh37.p13 chr15: 30,931,291-30,944,684 ARHGAP11B, LOC100288637
    nsv7064529inversion1nstd229human GRCh38 chr15: 30,725,264-31,634,528 , GRCh37.p13 chr15: 31,017,467-31,926,731 TRPM1, LINC02352, 18 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
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