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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6717253copy number variation1nstd229human GRCh38 chr3: 32,387,103-32,394,693 , GRCh37.p13 chr3: 32,428,595-32,436,185 CMTM7
    nsv6711897copy number variation1nstd229human GRCh38 chr3: 32,377,886-32,390,938 , GRCh37.p13 chr3: 32,419,378-32,432,430 CMTM7
    nsv6709930copy number variation1nstd229human GRCh38 chr3: 32,436,853-32,437,184 , GRCh37.p13 chr3: 32,478,345-32,478,676 CMTM7
    nsv6707420copy number variation1nstd229human GRCh38 chr3: 32,428,237-32,428,265 , GRCh37.p13 chr3: 32,469,729-32,469,757 CMTM7
    nsv6705076copy number variation1nstd229human GRCh38 chr3: 32,392,930-32,410,870 , GRCh37.p13 chr3: 32,434,422-32,452,362 CMTM7
    nsv6699715copy number variation1nstd229human GRCh38 chr3: 32,394,297-32,400,281 , GRCh37.p13 chr3: 32,435,789-32,441,773 CMTM7
    nsv6699451copy number variation1nstd229human GRCh38 chr3: 32,305,104-32,516,415 , GRCh37.p13 chr3: 32,346,596-32,557,907 MIR548AY, CMTM8, 3 more genes
    nsv6699033copy number variation1nstd229human GRCh38 chr3: 32,390,295-32,393,077 , GRCh37.p13 chr3: 32,431,787-32,434,569 CMTM7
    nsv6361030copy number variation1nstd223human GRCh38 chr3: 32,428,237-32,428,264 , GRCh37.p13 chr3: 32,469,729-32,469,756 CMTM7
    nsv6313891copy number variation1nstd102humanUncertain significance GRCh37 chr3: 31,859,973-33,127,072 , GRCh38.p12 chr3: 31,818,481-33,085,580 RPL30P4, RPL21P40, 22 more genes
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv6295004mobile element insertion1nstd186human GRCh37 chr3: 32,489,789-32,489,840 , GRCh38.p12 chr3: 32,448,297-32,448,348 CMTM7
    nsv6243596mobile element insertion1nstd215human GRCh38 chr3: 32,397,310-32,397,310 , GRCh37.p13 chr3: 32,438,802-32,438,802 CMTM7
    nsv6161106copy number variation1nstd214human GRCh38 chr3: 32,416,325-32,416,442 , GRCh37.p13 chr3: 32,457,817-32,457,934 CMTM7
    nsv6134843copy number variation1nstd213human GRCh37 chr3: 31,580,000-32,830,001 , GRCh38.p12 chr3: 31,538,508-32,788,509 GPD1L, CNOT10, 19 more genes
    nsv6063938insertion1nstd212human GRCh38 chr3: 32,397,296-32,397,296 , GRCh37.p13 chr3: 32,438,788-32,438,788 CMTM7
    nsv5951155insertion1nstd209human GRCh38 chr3: 32,397,296-32,397,296 , GRCh37.p13 chr3: 32,438,788-32,438,788 CMTM7
    nsv5902219copy number variation1nstd209human GRCh38 chr3: 32,416,325-32,416,442 , GRCh37.p13 chr3: 32,457,817-32,457,934 CMTM7
    nsv5889925copy number variation1nstd209human GRCh38 chr3: 32,428,137-32,428,196 , GRCh37.p13 chr3: 32,469,629-32,469,688 CMTM7
    nsv5685676mobile element insertion2nstd211human GRCh38 chr3: 32,397,310-32,397,310 , GRCh37.p13 chr3: 32,438,802-32,438,802 CMTM7
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