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Items: 1 to 20 of 141

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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
    nsv5449132copy number variation1nstd206human GRCh38 chr3: 127,537,459-127,552,228 , GRCh37.p13 chr3: 127,256,302-127,271,071 LINC01471, LINC02034
    nsv5434493copy number variation1nstd206human GRCh38 chr3: 127,528,768-127,537,337 , GRCh37.p13 chr3: 127,247,611-127,256,180 LINC02034, LINC01471
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4919981copy number variation1nstd200human GRCh38 chr3: 127,532,526-127,533,367 , GRCh37.p13 chr3: 127,251,369-127,252,210 LINC01471
    nsv4584791copy number variation1nstd183human GRCh37 chr3: 127,058,811-127,231,663 , GRCh38.p12 chr3: 127,339,968-127,512,820 LOC105374094, LINC02016, 1 more genes
    nsv4564593mobile element insertion1nstd166human GRCh37.p13 chr3: 127,220,365-127,220,365 , GRCh38.p12 chr3: 127,501,522-127,501,522 LINC01471
    nsv4521282copy number variation1nstd166human GRCh37.p13 chr3: 127,251,370-127,252,210 , GRCh38.p12 chr3: 127,532,527-127,533,367 LINC01471
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 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
    nsv3920834copy number variation1nstd102humanUncertain significance NCBI36 chr3: 127,308,312-142,119,621 , GRCh38 chr3: 126,106,779-140,918,089 , GRCh37 chr3: 125,825,622-140,636,931 NCK1-DT, LOC107986126, 271 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 more genes
    nsv3918094copy number variation1nstd102humanPathogenic NCBI36 chr3: 113,822,514-129,935,667 , GRCh38 chr3: 112,620,977-128,734,134 , GRCh37 chr3: 112,339,824-128,452,977 QTRT2, MIR544B, 284 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 RPL23AP49, DLEC1, 2875 more genes
    esv4011097complex chromosomal rearrangement6estd236human GRCh37 chr3: 125,695,543-174,724,062 , GRCh38.p12 chr3: 125,976,700-175,006,272 , AADAC, 733 more genes
    nsv3168810inversion1nstd158human GRCh37 chr3: 115,360,357-196,043,925 , GRCh38.p12 chr3: 115,641,510-196,317,054 , AADAC, 1298 more genes
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