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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076777inversion1nstd229human GRCh38 chr11: 114,180,972-114,778,739 , GRCh37.p13 chr11: 114,051,694-114,649,461 NNMT, NXPE4, 12 more genes
    nsv7069281inversion1nstd229human GRCh38 chr11: 107,936,485-114,400,629 , GRCh37.p13 chr11: 107,807,211-114,271,351 LRRC37A13P, POU2AF3, 121 more genes
    nsv7060444inversion1nstd229human GRCh38 chr11: 114,035,283-115,207,618 , GRCh37.p13 chr11: 113,906,005-115,078,338 CADM1, LOC105369506, 13 more genes
    nsv6914687copy number variation1nstd229human GRCh38 chr11: 114,397,627-114,416,953 , GRCh37.p13 chr11: 114,268,349-114,287,675 RBM7, C11orf71
    nsv6909591copy number variation1nstd229human GRCh38 chr11: 114,394,813-114,396,253 , GRCh37.p13 chr11: 114,265,535-114,266,975 C11orf71
    nsv6637811copy number variation1nstd102humanPathogenic GRCh37 chr11: 109,328,787-116,414,966 , GRCh38.p12 chr11: 109,458,061-116,544,249 LOC102723966, NXPE4, 129 more genes
    nsv6594188inversion1nstd223human GRCh38 chr11: 114,389,533-114,391,017 , GRCh37.p13 chr11: 114,260,255-114,261,739 C11orf71
    nsv6586218inversion1nstd223human GRCh38 chr11: 107,936,497-114,408,912 , GRCh37.p13 chr11: 107,807,223-114,279,634 LOC107984390, ATF4P4, 121 more genes
    nsv6579484inversion1nstd223human GRCh38 chr11: 114,039,971-117,481,220 , GRCh37.p13 chr11: 113,910,693-117,351,935 RNF214, LOC107984372, 52 more genes
    nsv6471311copy number variation1nstd223human GRCh38 chr11: 114,397,627-114,416,948 , GRCh37.p13 chr11: 114,268,349-114,287,670 RBM7, C11orf71
    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
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 more genes
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 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
    nsv6132343copy number variation1nstd213human GRCh37 chr11: 113,810,000-115,080,001 , GRCh38.p12 chr11: 113,939,278-115,209,281 HTR3B, RBM7, 15 more genes
    nsv6097455insertion1nstd212human GRCh38 chr11: 114,394,250-114,394,250 , GRCh37.p13 chr11: 114,264,972-114,264,972 C11orf71
    nsv6039458copy number variation1nstd212human GRCh38 chr11: 114,389,599-114,389,684 , GRCh37.p13 chr11: 114,260,321-114,260,406 C11orf71
    nsv5977858insertion1nstd209human GRCh38 chr11: 114,394,228-114,394,228 , GRCh37.p13 chr11: 114,264,950-114,264,950 C11orf71
    nsv5652858insertion1nstd207human GRCh38 chr11: 114,394,174-114,394,174 , GRCh37.p13 chr11: 114,264,896-114,264,896 C11orf71
    nsv5588704copy number variation1nstd207human GRCh38 chr11: 114,394,178-114,394,228 , GRCh37.p13 chr11: 114,264,900-114,264,950 C11orf71
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