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Items: 1 to 20 of 138

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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
    nsv5905274copy number variation1nstd209human GRCh38 chr3: 127,546,452-127,548,296 , GRCh37.p13 chr3: 127,265,295-127,267,139 LINC02034
    nsv5834892copy number variation1nstd209human GRCh38 chr3: 127,546,454-127,548,338 , GRCh37.p13 chr3: 127,265,297-127,267,181 LINC02034
    nsv5683357mobile element insertion1nstd211human GRCh38 chr3: 127,555,276-127,555,276 , GRCh37.p13 chr3: 127,274,119-127,274,119 LINC02034
    nsv5449132copy number variation1nstd206human GRCh38 chr3: 127,537,459-127,552,228 , GRCh37.p13 chr3: 127,256,302-127,271,071 LINC01471, LINC02034
    nsv5440459copy number variation1nstd206human GRCh38 chr3: 127,550,487-127,554,431 , GRCh37.p13 chr3: 127,269,330-127,273,274 LINC02034
    nsv5434493copy number variation1nstd206human GRCh38 chr3: 127,528,768-127,537,337 , GRCh37.p13 chr3: 127,247,611-127,256,180 LINC02034, LINC01471
    nsv5409971mobile element insertion1nstd206human GRCh38 chr3: 127,555,276-127,555,280 , GRCh37.p13 chr3: 127,274,119-127,274,123 LINC02034
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4919982copy number variation1nstd200human GRCh38 chr3: 127,550,487-127,554,431 , GRCh37.p13 chr3: 127,269,330-127,273,274 LINC02034
    nsv4807088copy number variation1nstd200human GRCh37 chr3: 127,269,330-127,273,274 , GRCh38.p12 chr3: 127,550,487-127,554,431 LINC02034
    nsv4807087copy number variation1nstd200human GRCh37 chr3: 127,266,669-127,266,960 , GRCh38.p12 chr3: 127,547,826-127,548,117 LINC02034
    nsv4585113copy number variation1nstd183human GRCh37 chr3: 127,269,325-127,273,274 , GRCh38.p12 chr3: 127,550,482-127,554,431 LINC02034
    nsv4468353mobile element insertion1nstd166human GRCh37.p13 chr3: 127,274,106-127,274,106 , GRCh38.p12 chr3: 127,555,263-127,555,263 LINC02034
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4107853copy number variation1nstd166human GRCh37.p13 chr3: 127,269,330-127,273,274 , GRCh38.p12 chr3: 127,550,487-127,554,431 LINC02034
    nsv4100195copy number variation1nstd166human GRCh37.p13 chr3: 127,268,988-127,280,769 , GRCh38.p12 chr3: 127,550,145-127,561,926 LINC02034
    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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