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Items: 1 to 20 of 114

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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
    nsv5437023copy number variation1nstd206human GRCh38 chr3: 127,574,657-127,575,045 , GRCh37.p13 chr3: 127,293,500-127,293,888 TPRA1, MIR6825
    nsv5346505translocation1nstd200human GRCh38 chr3: 127,578,104-127,578,104 , GRCh38 chr3: 127,576,809-127,576,809 , GRCh37.p13 chr3: 127,295,652-127,295,652 , GRCh37.p13 chr3: 127,296,947-127,296,947 TPRA1
    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
    nsv5096568mobile element insertion1nstd203human GRCh38 chr3: 127,593,711-127,593,728 , GRCh37.p13 chr3: 127,312,554-127,312,571 TPRA1
    nsv5095332mobile element insertion1nstd203human GRCh38 chr3: 127,582,654-127,582,731 , GRCh37.p13 chr3: 127,301,497-127,301,574 TPRA1
    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
    nsv4919984copy number variation1nstd200human GRCh38 chr3: 127,594,142-127,595,195 , GRCh37.p13 chr3: 127,312,985-127,314,038 TPRA1
    nsv4919983copy number variation1nstd200human GRCh38 chr3: 127,581,417-127,581,476 , GRCh37.p13 chr3: 127,300,260-127,300,319 TPRA1
    nsv4807090copy number variation1nstd200human GRCh37 chr3: 127,315,065-127,316,719 , GRCh38.p12 chr3: 127,596,222-127,597,876 MCM2, TPRA1
    nsv4807089copy number variation1nstd200human GRCh37 chr3: 127,295,652-127,296,947 , GRCh38.p12 chr3: 127,576,809-127,578,104 TPRA1
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4104533copy number variation1nstd166human GRCh37.p13 chr3: 127,295,652-127,296,947 , GRCh38.p12 chr3: 127,576,809-127,578,104 TPRA1
    nsv4098444copy number variation1nstd166human GRCh37.p13 chr3: 127,293,500-127,293,888 , GRCh38.p12 chr3: 127,574,657-127,575,045 MIR6825, TPRA1
    nsv3971060insertion1nstd168human GRCh38 chr3: 127,594,938-127,631,017 , GRCh37.p13 chr3: 127,313,781-127,349,860 MCM2, PODXL2, 2 more genes
    nsv3923961copy number variation1nstd102humanPathogenic GRCh38 chr3: 126,797,420-128,946,623 , GRCh37 chr3: 126,516,263-128,665,466 , NCBI36 chr3: 127,998,953-130,148,156 RUVBL1-AS1, LOC105374096, 49 more genes
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
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