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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112709copy number variation1nstd102humanPathogenic GRCh37 chr3: 123,000,000-129,700,000 , GRCh38.p12 chr3: 123,281,153-129,981,157 OR7E97P, MARK3P3, 160 more genes
    nsv6112688copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144 RNU4-62P, MTCO1P29, 169 more genes
    nsv5902731copy number variation1nstd209human GRCh38 chr3: 125,297,419-125,297,748 , GRCh37.p13 chr3: 125,016,263-125,016,592 ZNF148
    nsv5897708copy number variation1nstd209human GRCh38 chr3: 125,297,667-125,298,775 , GRCh37.p13 chr3: 125,016,511-125,017,619 ZNF148
    nsv5894446copy number variation1nstd209human GRCh38 chr3: 125,362,740-125,362,818 , GRCh37.p13 chr3: 125,081,584-125,081,662 ZNF148
    nsv5892131copy number variation1nstd209human GRCh38 chr3: 125,365,000-125,365,702 , GRCh37.p13 chr3: 125,083,844-125,084,546 ZNF148
    nsv5888745copy number variation1nstd209human GRCh38 chr3: 125,343,442-125,343,508 , GRCh37.p13 chr3: 125,062,286-125,062,352 ZNF148, DNAJB6P7
    nsv5683766mobile element insertion2nstd211human GRCh38 chr3: 125,266,301-125,266,301 , GRCh37.p13 chr3: 124,985,145-124,985,145 ZNF148
    nsv5678044mobile element insertion2nstd211human GRCh38 chr3: 125,254,197-125,254,197 , GRCh37.p13 chr3: 124,973,041-124,973,041 ZNF148
    nsv5572131copy number variation1nstd207human GRCh38 chr3: 125,297,423-125,297,750 , GRCh37.p13 chr3: 125,016,267-125,016,594 ZNF148
    nsv5565646copy number variation1nstd207human GRCh38 chr3: 125,343,442-125,343,508 , GRCh37.p13 chr3: 125,062,286-125,062,352 ZNF148, DNAJB6P7
    nsv5451132copy number variation1nstd206human GRCh38 chr3: 125,297,419-125,297,753 , GRCh37.p13 chr3: 125,016,263-125,016,597 ZNF148
    nsv5403022mobile element insertion1nstd206human GRCh38 chr3: 125,254,197-125,254,248 , GRCh37.p13 chr3: 124,973,041-124,973,092 ZNF148
    nsv5401027mobile element insertion1nstd206human GRCh38 chr3: 125,266,301-125,266,352 , GRCh37.p13 chr3: 124,985,145-124,985,196 ZNF148
    nsv5386949copy number variation1nstd186human GRCh37 chr3: 125,062,321-125,062,390 , GRCh38.p12 chr3: 125,343,477-125,343,546 ZNF148, DNAJB6P7
    nsv5386131copy number variation2nstd186human GRCh37 chr3: 125,016,263-125,016,597 , GRCh38.p12 chr3: 125,297,419-125,297,753 ZNF148
    nsv5321455translocation1nstd204human GRCh38.p13 chr3: 125,297,753-125,297,753 , GRCh38.p13 chr3: 125,297,419-125,297,419 , GRCh37.p13 chr3: 125,016,263-125,016,263 , GRCh37.p13 chr3: 125,016,597-125,016,597 ZNF148
    nsv5172075mobile element insertion1nstd203human GRCh38 chr3: 125,351,448-125,351,451 , GRCh37.p13 chr3: 125,070,292-125,070,295 ZNF148
    nsv5170994mobile element insertion1nstd203human GRCh38 chr3: 125,270,659-125,270,672 , GRCh37.p13 chr3: 124,989,503-124,989,516 ZNF148
    nsv5091719mobile element insertion1nstd203human GRCh38 chr3: 125,306,877-125,306,891 , GRCh37.p13 chr3: 125,025,721-125,025,735 ZNF148
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