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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094183copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,421-75,283,128 , GRCh38.p12 chr11: 71,435,375-75,572,083 LOC112268078, LRTOMT, 142 more genes
    nsv7076487inversion1nstd229human GRCh38 chr11: 73,984,249-73,989,663 , GRCh37.p13 chr11: 73,695,294-73,700,708 DPPA4P3
    nsv7073567inversion1nstd229human GRCh38 chr11: 73,812,649-75,298,624 , GRCh37.p13 chr11: 73,523,694-75,009,668 LIPT2, RNF169, 51 more genes
    nsv7072150inversion1nstd229human GRCh38 chr11: 73,682,578-73,990,508 , GRCh37.p13 chr11: 73,393,623-73,701,553 ARPC3P4, RN7SKP243, 9 more genes
    nsv7064187inversion1nstd229human GRCh38 chr11: 73,989,817-73,994,881 , GRCh37.p13 chr11: 73,700,862-73,705,926 LOC100421622, DPPA4P3
    nsv6899578copy number variation1nstd229human GRCh38 chr11: 73,891,401-74,051,200 , GRCh37.p13 chr11: 73,602,446-73,762,245 LOC100421622, UCP2, 6 more genes
    nsv6472363copy number variation1nstd223human GRCh38 chr11: 73,982,015-73,989,618 , GRCh37.p13 chr11: 73,693,060-73,700,663 UCP2, DPPA4P3
    nsv6457711copy number variation1nstd223human GRCh38 chr11: 73,967,136-73,989,707 , GRCh37.p13 chr11: 73,678,181-73,700,752 UCP2, DNAJB13, 1 more genes
    nsv6456980copy number variation1nstd223human GRCh38 chr11: 73,992,599-73,993,276 , GRCh37.p13 chr11: 73,703,644-73,704,321 LOC100421622, DPPA4P3
    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
    nsv6301353copy number variation1nstd186human GRCh37 chr11: 73,693,017-73,700,707 , GRCh38.p12 chr11: 73,981,972-73,989,662 DPPA4P3, UCP2
    nsv6110903inversion1nstd212human GRCh38 chr11: 73,984,249-73,989,663 , GRCh37.p13 chr11: 73,695,294-73,700,708 DPPA4P3
    nsv5863447copy number variation1nstd209human GRCh38 chr11: 73,981,939-73,989,451 , GRCh37.p13 chr11: 73,692,984-73,700,496 UCP2, DPPA4P3
    nsv5511514copy number variation1nstd206human GRCh38 chr11: 73,981,972-73,989,662 , GRCh37.p13 chr11: 73,693,017-73,700,707 DPPA4P3, UCP2
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5332835translocation1nstd200human GRCh37 chr11: 73,695,294-73,695,294 , GRCh37 chr11: 73,700,708-73,700,708 , GRCh38.p12 chr11: 73,984,249-73,984,249 , GRCh38.p12 chr11: 73,989,663-73,989,663 DPPA4P3
    nsv5190296mobile element insertion1nstd203human GRCh38 chr11: 73,988,720-73,988,729 , GRCh37.p13 chr11: 73,699,765-73,699,774 DPPA4P3
    nsv4577548mobile element insertion1nstd166human GRCh37.p13 chr11: 73,699,764-73,699,764 , GRCh38.p12 chr11: 73,988,719-73,988,719 DPPA4P3
    nsv4456614copy number variation1nstd102humanUncertain significance GRCh37 chr11: 73,395,712-73,788,461 , GRCh38.p12 chr11: 73,684,667-74,077,416 PAAF1, DNAJB13, 12 more genes
    nsv4455639copy number variation1nstd102humanUncertain significance GRCh37 chr11: 73,128,157-73,788,461 , GRCh38.p12 chr11: 73,417,112-74,077,416 RAB6A, UCP2, 16 more genes
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