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Items: 1 to 20 of 261

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066313inversion1nstd229human GRCh38 chr11: 6,624,146-15,294,249 , GRCh37.p13 chr11: 6,645,377-15,315,795 RNA5SP332, TMEM41B, 163 more genes
    nsv6917769copy number variation1nstd229human GRCh38 chr11: 10,664,635-10,677,420 , GRCh37.p13 chr11: 10,686,182-10,698,967 IRAG1
    nsv6917151copy number variation1nstd229human GRCh38 chr11: 9,940,109-18,580,574 , GRCh37.p13 chr11: 9,961,656-18,602,121 MYOD1, MIR8070, 139 more genes
    nsv6915956copy number variation1nstd229human GRCh38 chr11: 10,667,401-10,672,700 , GRCh37.p13 chr11: 10,688,948-10,694,247 IRAG1
    nsv6910589copy number variation1nstd229human GRCh38 chr11: 10,598,193-10,611,741 , GRCh37.p13 chr11: 10,619,740-10,633,288 IRAG1-AS1, IRAG1
    nsv6908628copy number variation1nstd229human GRCh38 chr11: 10,678,813-10,678,891 , GRCh37.p13 chr11: 10,700,360-10,700,438 IRAG1
    nsv6907871copy number variation1nstd229human GRCh38 chr11: 10,642,934-10,648,134 , GRCh37.p13 chr11: 10,664,481-10,669,681 IRAG1
    nsv6904095copy number variation1nstd229human GRCh38 chr11: 10,674,783-10,675,003 , GRCh37.p13 chr11: 10,696,330-10,696,550 IRAG1
    nsv6900807copy number variation1nstd229human GRCh38 chr11: 10,673,520-10,678,073 , GRCh37.p13 chr11: 10,695,067-10,699,620 IRAG1
    nsv6898661copy number variation1nstd229human GRCh38 chr11: 10,617,909-10,617,939 , GRCh37.p13 chr11: 10,639,456-10,639,486 IRAG1
    nsv6584475inversion1nstd223human GRCh38 chr11: 10,616,686-10,617,315 , GRCh37.p13 chr11: 10,638,233-10,638,862 IRAG1
    nsv6578417inversion1nstd223human GRCh38 chr11: 7,263,807-16,565,752 , GRCh37.p13 chr11: 7,285,038-16,587,299 TEAD1, IRAG1, 151 more genes
    nsv6439816copy number variation1nstd223human GRCh38 chr11: 10,586,782-10,586,793 , GRCh37.p13 chr11: 10,608,329-10,608,340 IRAG1-AS1, IRAG1
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6247766mobile element insertion1nstd215human GRCh38 chr11: 10,615,946-10,615,946 , GRCh37.p13 chr11: 10,637,493-10,637,493 IRAG1
    nsv6204870copy number variation1nstd214human GRCh38 chr11: 10,680,348-10,680,403 , GRCh37.p13 chr11: 10,701,895-10,701,950 IRAG1
    nsv6190999copy number variation1nstd214human GRCh38 chr11: 10,680,329-10,680,523 , GRCh37.p13 chr11: 10,701,876-10,702,070 IRAG1
    nsv6094369insertion1nstd212human GRCh38 chr11: 10,680,370-10,680,370 , GRCh37.p13 chr11: 10,701,917-10,701,917 IRAG1
    nsv6088436insertion1nstd212human GRCh38 chr11: 10,615,935-10,615,935 , GRCh37.p13 chr11: 10,637,482-10,637,482 IRAG1
    nsv6032741copy number variation1nstd212human GRCh38 chr11: 10,615,948-10,616,023 , GRCh37.p13 chr11: 10,637,495-10,637,570 IRAG1
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