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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096931copy number variation2nstd102humanUncertain significance GRCh37 chr3: 126,707,437-130,720,194 , GRCh38.p12 chr3: 126,988,594-131,001,350 JMJD4P1, MARK2P19, 104 more genes
    nsv7043614inversion1nstd229human GRCh38 chr3: 126,481,308-130,612,264 , GRCh37.p13 chr3: 126,200,151-130,331,108 SNRPCP8, CNBP, 106 more genes
    nsv7041415inversion1nstd229human GRCh38 chr3: 128,855,871-129,481,105 , GRCh37.p13 chr3: 128,574,714-129,199,948 CFAP92, H1-10, 24 more genes
    nsv7038944inversion1nstd229human GRCh38 chr3: 125,715,935-130,031,043 , GRCh37.p13 chr3: 125,434,863-129,749,886 H1-8, FBRSL1P1, 123 more genes
    nsv6721691copy number variation1nstd229human GRCh38 chr3: 129,376,917-129,464,454 , GRCh37.p13 chr3: 129,095,760-129,183,297 RPL32P3, IFT122, 3 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6566785inversion1nstd223human GRCh38 chr3: 125,931,297-130,096,571 , GRCh37.p13 chr3: 125,650,140-129,815,414 MIR6826, RN7SL698P, 114 more genes
    nsv6563554inversion1nstd223human GRCh38 chr3: 126,481,307-130,612,263 , GRCh37.p13 chr3: 126,200,150-130,331,107 METTL5P2, EFCC1, 106 more genes
    nsv6311770copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,365,818-133,465,047 , GRCh38.p12 chr3: 120,646,971-133,746,203 HNRNPA1P23, MIX23, 278 more genes
    nsv6134783copy number variation1nstd213human GRCh37 chr3: 128,240,000-130,600,001 , GRCh38.p12 chr3: 128,521,157-130,881,157 FTH1P4, GP9, 68 more genes
    nsv6134575copy number variation1nstd213human GRCh37 chr3: 116,870,000-132,100,001 , GRCh38.p12 chr3: 117,151,153-132,381,157 ACP3, ADCY5, 308 more genes
    nsv6134399copy number variation1nstd213human GRCh37 chr3: 128,260,000-129,620,001 , GRCh38.p12 chr3: 128,541,157-129,901,158 FTH1P4, GP9, 43 more genes
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 RNU6-789P, FAM86HP, 169 more genes
    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
    nsv5451171copy number variation1nstd206human GRCh38 chr3: 129,380,519-129,487,453 , GRCh37.p13 chr3: 129,099,362-129,206,296 IFT122, EFCAB12, 3 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4914756copy number variation1nstd200human GRCh38 chr3: 129,384,416-129,491,454 , GRCh37.p13 chr3: 129,103,259-129,210,297 IFT122, EFCAB12, 3 more genes
    nsv4682966copy number variation1nstd102humanUncertain significance GRCh37 chr3: 128,889,296-129,270,183 , GRCh38.p12 chr3: 129,170,453-129,551,340 RPL32P3, NUP210P3, 17 more genes
    nsv4403535copy number variation1nstd174human GRCh37 chr3: 129,099,664-129,213,583 , GRCh38.p12 chr3: 129,380,821-129,494,740 MBD4, SNORA7B, 3 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
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