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Items: 1 to 20 of 175

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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
    nsv7074892inversion1nstd229human GRCh38 chr11: 114,204,315-114,261,358 , GRCh37.p13 chr11: 114,075,037-114,132,080 NNMT, ZBTB16
    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
    nsv6915250copy number variation1nstd229human GRCh38 chr11: 114,271,891-114,275,669 , GRCh37.p13 chr11: 114,142,613-114,146,391 NNMT
    nsv6905397copy number variation1nstd229human GRCh38 chr11: 114,294,846-114,321,438 , GRCh37.p13 chr11: 114,165,568-114,192,160 NNMT
    nsv6902077copy number variation1nstd229human GRCh38 chr11: 114,271,889-114,275,686 , GRCh37.p13 chr11: 114,142,611-114,146,408 NNMT
    nsv6900588copy number variation1nstd229human GRCh38 chr11: 114,308,403-114,312,448 , GRCh37.p13 chr11: 114,179,125-114,183,170 NNMT
    nsv6900045copy number variation1nstd229human GRCh38 chr11: 114,288,302-114,292,940 , GRCh37.p13 chr11: 114,159,024-114,163,662 NNMT
    nsv6898790copy number variation1nstd229human GRCh38 chr11: 114,293,901-114,302,600 , GRCh37.p13 chr11: 114,164,623-114,173,322 NNMT
    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
    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
    nsv6473459copy number variation1nstd223human GRCh38 chr11: 114,271,889-114,275,668 , GRCh37.p13 chr11: 114,142,611-114,146,390 NNMT
    nsv6455601copy number variation1nstd223human GRCh38 chr11: 114,260,504-114,261,309 , GRCh37.p13 chr11: 114,131,226-114,132,031 NNMT
    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
    nsv6258357mobile element insertion1nstd215human GRCh38 chr11: 114,269,952-114,269,952 , GRCh37.p13 chr11: 114,140,674-114,140,674 NNMT
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