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Items: 1 to 20 of 953

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130311insertion1nstd186human GRCh37 chr15: 31,338,471-31,338,481 , GRCh38.p12 chr15|NT_187660.1: 3,332,027-3,332,037 , GRCh38.p12 chr15: 31,046,268-31,046,278 , GRCh38.p12 chr15|NW_011332701.1: 3,219,575-3,219,585 TRPM1
    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
    nsv5973891inversion1nstd209human GRCh38 chr15: 31,080,721-31,084,984 , GRCh37.p13 chr15: 31,372,924-31,377,187 TRPM1
    nsv5973188inversion1nstd209human GRCh38 chr15: 30,730,483-31,672,938 , GRCh37.p13 chr15: 31,022,686-31,965,141 , TRPM1, 21 more genes
    nsv5971903insertion1nstd209human GRCh38 chr15: 31,046,269-31,046,269 , GRCh37.p13 chr15: 31,338,472-31,338,472 TRPM1
    nsv5945748copy number variation1nstd209human GRCh38 chr15: 31,016,368-31,016,512 , GRCh37.p13 chr15: 31,308,571-31,308,715 TRPM1
    nsv5944226copy number variation1nstd209human GRCh38 chr15: 31,155,117-31,158,985 , GRCh37.p13 chr15: 31,447,320-31,451,188 TRPM1
    nsv5933691copy number variation1nstd209human GRCh38 chr15: 31,070,238-31,074,120 , GRCh37.p13 chr15: 31,362,441-31,366,323 TRPM1
    nsv5855520copy number variation1nstd209human GRCh38 chr15: 31,070,412-31,074,141 , GRCh37.p13 chr15: 31,362,615-31,366,344 TRPM1
    nsv5852031copy number variation1nstd209human GRCh38 chr15: 31,155,093-31,159,037 , GRCh37.p13 chr15: 31,447,296-31,451,240 TRPM1
    nsv5850230copy number variation1nstd209human GRCh38 chr15: 31,080,437-31,088,965 , GRCh37.p13 chr15: 31,372,640-31,381,168 TRPM1
    nsv5726569mobile element insertion1nstd211human GRCh38 chr15: 31,145,601-31,145,601 , GRCh37.p13 chr15: 31,437,804-31,437,804 TRPM1
    nsv5713755mobile element insertion1nstd211human GRCh38 chr15: 31,073,924-31,073,924 , GRCh37.p13 chr15: 31,366,127-31,366,127 TRPM1
    nsv5672819copy number variation1nstd102humanPathogenic GRCh37 chr15: 31,355,301-31,369,124 , GRCh38.p12 chr15|NT_187660.1: 3,348,868-3,362,668 , GRCh38.p12 chr15: 31,063,098-31,076,921 , GRCh38.p12 chr15|NW_011332701.1: 3,236,416-3,250,216 TRPM1, MIR211
    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
    nsv5564382copy number variation1nstd102humanUncertain significance GRCh37 chr15: 31,327,749-31,327,877 , GRCh38.p12 chr15: 31,035,546-31,035,674 , GRCh38.p12 chr15|NT_187660.1: 3,321,304-3,321,432 , GRCh38.p12 chr15|NW_011332701.1: 3,208,852-3,208,980 TRPM1, LOC105370752
    nsv5550320insertion1nstd206human GRCh38 chr15: 31,046,268-31,046,278 , GRCh37.p13 chr15: 31,338,471-31,338,481 TRPM1
    nsv5512570copy number variation1nstd206human GRCh38 chr15: 31,155,121-31,158,986 , GRCh37.p13 chr15: 31,447,324-31,451,189 TRPM1
    nsv5511588copy number variation1nstd206human GRCh38 chr15: 31,004,353-31,007,868 , GRCh37.p13 chr15: 31,296,556-31,300,071 TRPM1
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