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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112769copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,935,243-32,445,105 , GRCh38.p12 chr15: 30,643,040-32,152,904 LOC101930434, MTMR10, 21 more genes
    nsv5973188inversion1nstd209human GRCh38 chr15: 30,730,483-31,672,938 , GRCh37.p13 chr15: 31,022,686-31,965,141 , TRPM1, 21 more genes
    nsv5937316copy number variation1nstd209human GRCh38 chr15: 30,929,717-30,929,796 , GRCh37.p13 chr15: 31,221,920-31,221,999 FAN1, MTMR10
    nsv5672663copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr15: 31,196,867-32,404,120 , GRCh38.p12 chr15|NT_187660.1: 3,190,396-4,397,060 , GRCh38.p12 chr15: 30,904,664-32,111,919 , GRCh38.p12 chr15|NW_011332701.1: 3,077,944-4,284,608 MTMR10, CHRNA7, 16 more genes
    nsv5669724inversion1nstd207human GRCh38 chr15: 30,618,104-32,153,204 , GRCh37.p13 chr15: 30,910,307-32,445,405 , CHRNA7, 26 more genes
    nsv5593228copy number variation1nstd207human GRCh38 chr15: 30,929,717-30,929,796 , GRCh37.p13 chr15: 31,221,920-31,221,999 FAN1, MTMR10
    nsv5316930copy number variation1nstd204human GRCh38.p13 chr15: 30,744,529-31,004,147 , GRCh37.p13 chr15: 31,036,732-31,296,350 , TRPM1, 9 more genes
    nsv5304878copy number variation1nstd204human GRCh38.p13 chr15: 30,931,835-30,935,456 , GRCh37.p13 chr15: 31,224,038-31,227,659 MTMR10, FAN1
    nsv5277224copy number variation1nstd204human GRCh38.p13 chr15: 30,847,257-30,902,235 , GRCh37.p13 chr15: 31,139,460-31,194,438 FAN1, TMEM183AP3
    nsv5275224copy number variation1nstd204human GRCh38.p13 chr15: 30,917,256-30,920,826 , GRCh37.p13 chr15: 31,209,459-31,213,029 FAN1, MTMR10
    nsv5270090copy number variation1nstd204human GRCh38.p13 chr15: 30,932,118-30,935,067 , GRCh37.p13 chr15: 31,224,321-31,227,270 MTMR10, FAN1
    nsv5268229copy number variation1nstd204human GRCh38.p13 chr15: 30,931,540-30,964,663 , GRCh37.p13 chr15: 31,223,743-31,256,866 FAN1, MTMR10, 1 more genes
    nsv5200372copy number variation2nstd102humanPathogenic GRCh37 chr15: 30,943,903-32,510,863 , GRCh38.p12 chr15: 30,651,700-32,218,662 TRPM1, LOC102724078, 21 more genes
    nsv5200367copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,208,842-28,525,460 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,280,314 SNORD115-27, LOC105370747, 246 more genes
    nsv5200365copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,652,489-32,438,943 , GRCh38.p12 chr15: 30,360,286-32,146,742 LOC105376704, RN7SL82P, 38 more genes
    nsv5144244mobile element insertion1nstd203human GRCh38 chr15: 30,910,962-30,910,974 , GRCh37.p13 chr15: 31,203,165-31,203,177 FAN1
    nsv5005241copy number variation1nstd200human GRCh38 chr15: 30,932,019-30,935,261 , GRCh37.p13 chr15: 31,224,222-31,227,464 FAN1, MTMR10
    nsv5001112copy number variation1nstd200human GRCh38 chr15: 30,942,615-30,944,063 , GRCh37.p13 chr15: 31,234,818-31,236,266 FAN1, MTMR10
    nsv5001111copy number variation1nstd200human GRCh38 chr15: 30,913,982-30,916,254 , GRCh37.p13 chr15: 31,206,185-31,208,457 FAN1
    nsv4863721copy number variation1nstd200human GRCh37 chr15: 31,224,222-31,227,464 , GRCh38.p12 chr15: 30,932,019-30,935,261 , GRCh38.p12 chr15|NW_011332701.1: 3,105,299-3,108,542 , GRCh38.p12 chr15|NT_187660.1: 3,217,751-3,220,994 MTMR10, FAN1
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