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Items: 1 to 20 of 199

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7065616inversion1nstd229human GRCh38 chr11: 55,877,934-56,853,091 , GRCh37.p13 chr11: 55,645,410-56,620,567 OR5M5P, OR5G3, 74 more genes
    nsv7064532inversion1nstd229human GRCh38 chr11: 55,878,162-56,072,221 , GRCh37.p13 chr11: 55,645,638-55,839,697 OR7E5P, OR5I1, 12 more genes
    nsv6912549copy number variation1nstd229human GRCh38 chr11: 55,917,267-56,071,129 , GRCh37.p13 chr11: 55,684,743-55,838,605 OR7E5P, OR5I1, 8 more genes
    nsv6903817copy number variation1nstd229human GRCh38 chr11: 55,889,039-57,077,059 , GRCh37.p13 chr11: 55,656,515-56,844,534 OR5J1P, OR8H1, 83 more genes
    nsv6621249copy number variation1nstd224human GRCh37 chr11: 55,171,027-56,905,911 , GRCh38.p12 chr11: 55,403,551-57,138,437 OR5I1, OR8K2P, 113 more genes
    nsv6621189copy number variation1nstd224human GRCh37 chr11: 55,659,089-55,762,038 , GRCh38.p12 chr11: 55,891,613-55,994,562 OR5I1, OR5W1P, 7 more genes
    nsv6621186copy number variation2nstd224human GRCh37 chr11: 54,794,237-56,003,589 , GRCh38.p12 chr11: 55,026,761-56,236,113 OR5L2, OR9M1P, 65 more genes
    nsv6578868inversion1nstd223human GRCh38 chr11: 55,977,216-55,977,408 , GRCh37.p13 chr11: 55,744,692-55,744,884 OR7E5P
    nsv6474423copy number variation1nstd223human GRCh38 chr11: 55,874,701-55,980,800 , GRCh37.p13 chr11: 55,642,177-55,748,276 TRIM51, OR10AK1P, 8 more genes
    nsv6474230copy number variation1nstd223human GRCh38 chr11: 55,982,098-55,982,619 , GRCh37.p13 chr11: 55,749,574-55,750,095 OR7E5P
    nsv6459401copy number variation1nstd223human GRCh38 chr11: 55,917,273-56,059,152 , GRCh37.p13 chr11: 55,684,749-55,826,628 OR5I1, OR5F2P, 7 more genes
    nsv6457619copy number variation1nstd223human GRCh38 chr11: 55,985,601-55,991,800 , GRCh37.p13 chr11: 55,753,077-55,759,276 OR7E5P, OR5F1
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6227925insertion1nstd214human GRCh38 chr11: 55,981,722-55,981,722 , GRCh37.p13 chr11: 55,749,198-55,749,198 OR7E5P
    nsv6143732copy number variation1nstd206human GRCh38 chr11: 55,917,274-56,071,016 , GRCh37.p13 chr11: 55,684,750-55,838,492 OR10AF1P, OR5AQ1P, 8 more genes
    nsv6132110copy number variation1nstd213human GRCh37 chr11: 55,660,000-55,830,001 , GRCh38.p12 chr11: 55,892,524-56,062,525 OR5W1P, OR5AQ1P, 9 more genes
    nsv6131996copy number variation1nstd213human GRCh37 chr11: 55,349,448-55,758,508 , GRCh38.p12 chr11: 55,581,972-55,991,032 OR5D3P, OR5D2P, 25 more genes
    nsv6101017inversion1nstd212human GRCh38 chr11: 54,578,670-59,501,927 , GRCh37.p13 chr11: 54,711,406-59,269,400 , APLNR, 236 more genes
    nsv5914325copy number variation1nstd209human GRCh38 chr11: 55,273,256-58,053,631 , GRCh37.p13 chr11: 55,040,732-57,821,103 , LOC107984365, 161 more genes
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