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Items: 1 to 20 of 301

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096932copy number variation1nstd102humanUncertain significance GRCh37 chr3: 129,150,344-129,159,234 , GRCh38.p12 chr3: 129,431,501-129,440,391 MBD4, IFT122
    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
    nsv6734657copy number variation1nstd229human GRCh38 chr3: 129,409,401-129,470,800 , GRCh37.p13 chr3: 129,128,244-129,189,643 IFT122, EFCAB12, 1 more genes
    nsv6731670copy number variation1nstd229human GRCh38 chr3: 129,440,849-129,518,444 , GRCh37.p13 chr3: 129,159,692-129,237,287 IFT122
    nsv6725920copy number variation1nstd229human GRCh38 chr3: 129,470,132-129,479,037 , GRCh37.p13 chr3: 129,188,975-129,197,880 IFT122
    nsv6724192copy number variation1nstd229human GRCh38 chr3: 129,463,105-129,470,714 , GRCh37.p13 chr3: 129,181,948-129,189,557 IFT122
    nsv6722931copy number variation1nstd229human GRCh38 chr3: 129,444,364-129,448,324 , GRCh37.p13 chr3: 129,163,207-129,167,167 IFT122
    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
    nsv6721478copy number variation1nstd229human GRCh38 chr3: 129,463,448-129,473,480 , GRCh37.p13 chr3: 129,182,291-129,192,323 IFT122
    nsv6720764copy number variation1nstd229human GRCh38 chr3: 129,470,428-129,479,910 , GRCh37.p13 chr3: 129,189,271-129,198,753 IFT122
    nsv6720481copy number variation1nstd229human GRCh38 chr3: 129,473,245-129,475,760 , GRCh37.p13 chr3: 129,192,088-129,194,603 IFT122
    nsv6720167copy number variation1nstd229human GRCh38 chr3: 129,460,435-129,460,618 , GRCh37.p13 chr3: 129,179,278-129,179,461 IFT122
    nsv6719941copy number variation1nstd229human GRCh38 chr3: 129,511,637-129,514,656 , GRCh37.p13 chr3: 129,230,480-129,233,499 IFT122
    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
    nsv6628640copy number variation1nstd224human GRCh37 chr3: 129,123,129-129,211,038 , GRCh38.p12 chr3: 129,404,286-129,492,195 EFCAB12, IFT122, 1 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
    nsv6564884inversion1nstd223human GRCh38 chr3: 129,444,580-129,445,209 , GRCh37.p13 chr3: 129,163,423-129,164,052 IFT122
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