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Items: 1 to 20 of 88

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5700328mobile element insertion2nstd211human GRCh38 chr11: 16,742,727-16,742,727 , GRCh37.p13 chr11: 16,764,274-16,764,274 C11orf58
    nsv5507673copy number variation1nstd206human GRCh38 chr11: 16,359,999-20,627,000 , GRCh37.p13 chr11: 16,381,545-20,648,546 , CSRP3, 102 more genes
    nsv5503168copy number variation1nstd206human GRCh38 chr11: 16,758,051-16,758,151 , GRCh37.p13 chr11: 16,779,598-16,779,698 C11orf58
    nsv5404744mobile element insertion1nstd206human GRCh38 chr11: 16,742,727-16,742,778 , GRCh37.p13 chr11: 16,764,274-16,764,325 C11orf58
    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
    nsv5192427mobile element insertion1nstd203human GRCh38 chr11: 16,756,587-16,756,605 , GRCh37.p13 chr11: 16,778,134-16,778,152 C11orf58
    nsv5136517mobile element insertion1nstd203human GRCh38 chr11: 16,742,712-16,742,727 , GRCh37.p13 chr11: 16,764,259-16,764,274 C11orf58
    nsv5136508mobile element insertion1nstd203human GRCh38 chr11: 16,754,547-16,754,585 , GRCh37.p13 chr11: 16,776,094-16,776,132 C11orf58
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4675502copy number variation1nstd102humanPathogenic GRCh37 chr11: 13,970,757-27,565,888 , GRCh38.p12 chr11: 13,949,210-27,544,341 MRGPRX5P, LDHC, 171 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
    nsv4602194copy number variation1nstd183human GRCh37 chr11: 16,760,318-16,761,128 , GRCh38.p12 chr11: 16,738,771-16,739,581 SOX6, C11orf58
    nsv4570723sequence alteration1nstd166human GRCh37.p13 chr11: 16,763,405-16,763,406 , GRCh38.p12 chr11: 16,741,858-16,741,859 C11orf58
    nsv4496962mobile element insertion1nstd166human GRCh37.p13 chr11: 16,767,858-16,767,858 , GRCh38.p12 chr11: 16,746,311-16,746,311 C11orf58
    nsv4491078mobile element insertion1nstd166human GRCh37.p13 chr11: 16,764,259-16,764,259 , GRCh38.p12 chr11: 16,742,712-16,742,712 C11orf58
    nsv4456716copy number variation1nstd102humanUncertain significance GRCh37 chr11: 16,775,884-18,418,719 , GRCh38.p12 chr11: 16,754,337-18,397,172 RNU6-593P, SNORD14A, 47 more genes
    nsv4455290copy number variation1nstd102humanUncertain significance GRCh37 chr11: 16,436,272-18,064,677 , GRCh38.p12 chr11: 16,414,726-18,043,130 LOC105376571, PIK3C2A, 30 more genes
    nsv4198253copy number variation1nstd166human GRCh37.p13 chr11: 16,779,598-16,779,698 , GRCh38.p12 chr11: 16,758,051-16,758,151 C11orf58
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