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Items: 1 to 20 of 278

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 VSIG10L2, OR8B6P, 268 more genes
    nsv7077728inversion1nstd229human GRCh38 chr11: 124,239,803-134,089,458 , GRCh37.p13 chr11: 124,110,545-133,959,353 LOC283172, PPP1R10P1, 175 more genes
    nsv6915552copy number variation1nstd229human GRCh38 chr11: 129,850,264-129,862,166 , GRCh37.p13 chr11: 129,720,159-129,732,061 TMEM45B, NFRKB
    nsv6913836copy number variation1nstd229human GRCh38 chr11: 129,868,637-129,869,579 , GRCh37.p13 chr11: 129,738,532-129,739,474 NFRKB
    nsv6912521copy number variation1nstd229human GRCh38 chr11: 129,883,758-129,883,776 , GRCh37.p13 chr11: 129,753,653-129,753,671 NFRKB
    nsv6904596copy number variation1nstd229human GRCh38 chr11: 129,891,263-129,912,688 , GRCh37.p13 chr11: 129,761,158-129,782,583 PRDM10, NFRKB
    nsv6898516copy number variation1nstd229human GRCh38 chr11: 129,835,330-129,885,593 , GRCh37.p13 chr11: 129,705,225-129,755,488 NFRKB, TMEM45B
    nsv6637558copy number variation1nstd102humanPathogenic GRCh37 chr11: 122,975,824-134,938,470 , GRCh38.p12 chr11: 123,105,116-135,068,576 OR8B8, LOC107984373, 234 more genes
    nsv6634467copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 127,074,235-135,006,516 , GRCh38.p12 chr11: 127,204,340-135,076,622 APLP2, BAK1P2, 98 more genes
    nsv6620700copy number variation1nstd224human GRCh37 chr11: 129,719,900-129,743,891 , GRCh38.p12 chr11: 129,850,005-129,873,996 TMEM45B, NFRKB
    nsv6474031copy number variation1nstd223human GRCh38 chr11: 129,850,264-129,862,163 , GRCh37.p13 chr11: 129,720,159-129,732,058 TMEM45B, NFRKB
    nsv6473700copy number variation1nstd223human GRCh38 chr11: 129,868,637-129,869,579 , GRCh37.p13 chr11: 129,738,532-129,739,474 NFRKB
    nsv6469719copy number variation1nstd223human GRCh38 chr11: 129,878,865-129,879,329 , GRCh37.p13 chr11: 129,748,760-129,749,224 NFRKB
    nsv6468076copy number variation1nstd223human GRCh38 chr11: 129,893,588-129,894,321 , GRCh37.p13 chr11: 129,763,483-129,764,216 NFRKB
    nsv6463924copy number variation1nstd223human GRCh38 chr11: 129,893,001-129,898,300 , GRCh37.p13 chr11: 129,762,896-129,768,195 PRDM10, NFRKB
    nsv6456803copy number variation1nstd223human GRCh38 chr11: 129,870,441-129,872,825 , GRCh37.p13 chr11: 129,740,336-129,742,720 NFRKB
    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
    nsv6315090copy number variation1nstd102humanPathogenic GRCh37 chr11: 128,634,685-134,257,741 , GRCh38.p12 chr11: 128,764,790-134,387,847 BAK1P2, RN7SL167P, 73 more genes
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv6258491mobile element insertion1nstd215human GRCh38 chr11: 129,889,661-129,889,661 , GRCh37.p13 chr11: 129,759,556-129,759,556 NFRKB
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