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Items: 1 to 20 of 142

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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
    nsv5578420copy number variation1nstd207human GRCh38 chr3: 127,611,674-127,611,999 , GRCh37.p13 chr3: 127,330,517-127,330,842 MCM2
    nsv5436799copy number variation1nstd206human GRCh38 chr3: 127,611,687-127,612,000 , GRCh37.p13 chr3: 127,330,530-127,330,843 MCM2
    nsv5384826mobile element deletion2nstd186human GRCh37 chr3: 127,330,530-127,330,843 , GRCh38.p12 chr3: 127,611,687-127,612,000 MCM2
    nsv5312912copy number variation1nstd204human GRCh37.p13 chr3: 127,310,233-127,320,569 , GRCh38.p13 chr3: 127,591,390-127,601,726 TPRA1, MCM2
    nsv5237601copy number variation1nstd204human GRCh38.p13 chr3: 127,591,670-127,601,591 , GRCh37.p13 chr3: 127,310,513-127,320,434 MCM2, TPRA1
    nsv5219678mobile element deletion1nstd204human GRCh38.p13 chr3: 127,611,684-127,612,002 , GRCh37.p13 chr3: 127,330,527-127,330,845 MCM2
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4919985copy number variation1nstd200human GRCh38 chr3: 127,596,222-127,597,876 , GRCh37.p13 chr3: 127,315,065-127,316,719 MCM2, TPRA1
    nsv4876312mobile element deletion1nstd200human GRCh38 chr3: 127,611,687-127,612,000 , GRCh37.p13 chr3: 127,330,530-127,330,843 MCM2
    nsv4807090copy number variation1nstd200human GRCh37 chr3: 127,315,065-127,316,719 , GRCh38.p12 chr3: 127,596,222-127,597,876 MCM2, TPRA1
    nsv4777882mobile element deletion1nstd200human GRCh37 chr3: 127,330,530-127,330,843 , GRCh38.p12 chr3: 127,611,687-127,612,000 MCM2
    nsv4709088copy number variation2nstd195human GRCh37 chr3: 127,330,517-127,330,518 , GRCh38.p12 chr3: 127,611,674-127,611,675 MCM2
    nsv4648156copy number variation1nstd186human GRCh37 chr3: 127,330,453-127,330,843 , GRCh38.p12 chr3: 127,611,610-127,612,000 MCM2
    nsv4638182mobile element deletion1nstd186human GRCh37 chr3: 127,330,518-127,330,843 , GRCh38.p12 chr3: 127,611,675-127,612,000 MCM2
    nsv4521714copy number variation1nstd166human GRCh37.p13 chr3: 127,330,469-127,330,562 , GRCh38.p12 chr3: 127,611,626-127,611,719 MCM2
    nsv4520290copy number variation1nstd166human GRCh37.p13 chr3: 127,330,453-127,330,843 , GRCh38.p12 chr3: 127,611,610-127,612,000 MCM2
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4110837copy number variation1nstd166human GRCh37.p13 chr3: 127,331,578-127,333,069 , GRCh38.p12 chr3: 127,612,735-127,614,226 MCM2
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