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Items: 1 to 20 of 95

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5915570copy number variation1nstd209human GRCh38 chr11: 61,477,122-61,488,222 , GRCh37.p13 chr11: 61,244,594-61,255,694 SAXO4
    nsv5852932copy number variation1nstd209human GRCh38 chr11: 61,482,102-61,483,293 , GRCh37.p13 chr11: 61,249,574-61,250,765 SAXO4
    nsv5851459copy number variation1nstd209human GRCh38 chr11: 61,477,056-61,488,090 , GRCh37.p13 chr11: 61,244,528-61,255,562 SAXO4
    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
    nsv5325627inversion1nstd204human GRCh37.p13 chr11: 58,669,453-61,321,541 , GRCh38.p13 chr11: 58,901,980-61,554,069 , CD5, 118 more genes
    nsv4885672inversion1nstd200human GRCh37 chr11: 58,669,461-61,321,541 , GRCh38.p12 chr11: 58,901,988-61,554,069 , MS4A2, 118 more genes
    nsv4841352copy number variation1nstd200human GRCh37 chr11: 61,244,564-61,255,644 , GRCh38.p12 chr11: 61,477,092-61,488,172 SAXO4
    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
    nsv4675148copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,385,382-62,456,278 , GRCh38.p12 chr11: 60,617,909-62,688,806 LOC105369326, MS4A18, 91 more genes
    nsv4672173copy number variation1nstd186human GRCh37 chr11: 61,253,822-61,253,866 , GRCh38.p12 chr11: 61,486,350-61,486,394 SAXO4
    nsv4611445copy number variation1nstd183human GRCh37 chr11: 61,253,822-61,253,866 , GRCh38.p12 chr11: 61,486,350-61,486,394 SAXO4
    nsv4603350copy number variation1nstd183human GRCh37 chr11: 61,238,220-61,262,732 , GRCh38.p12 chr11: 61,470,748-61,495,260 SAXO4
    nsv4457060copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,499,486-61,529,578 , GRCh38.p12 chr11: 60,732,013-61,762,106 TMEM109, LOC101927495, 41 more genes
    nsv4211377copy number variation1nstd166human GRCh37.p13 chr11: 61,244,850-61,255,500 , GRCh38.p12 chr11: 61,477,378-61,488,028 SAXO4
    nsv4208305copy number variation1nstd166human GRCh37.p13 chr11: 61,252,325-61,258,906 , GRCh38.p12 chr11: 61,484,853-61,491,434 SAXO4
    nsv4201996copy number variation1nstd166human GRCh37.p13 chr11: 61,249,863-61,250,206 , GRCh38.p12 chr11: 61,482,391-61,482,734 SAXO4
    nsv3915850copy number variation1nstd102humanLikely benign GRCh37 chr11: 61,177,001-61,588,631 , GRCh38 chr11: 61,409,529-61,821,159 , NCBI36 chr11: 60,933,577-61,345,207 TMEM258, RN7SL23P, 18 more genes
    nsv3912748copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,948,809-61,284,302 , NCBI36 chr11: 60,705,385-61,040,878 , GRCh38 chr11: 61,181,337-61,516,830 DDB1, LOC105369329, 15 more genes
    nsv3912126copy number variation1nstd102humanUncertain significance NCBI36 chr11: 60,798,467-61,166,648 , GRCh37.p13 chr11: 61,041,891-61,410,072 , GRCh38.p12 chr11: 61,274,419-61,642,600 DDB1, LOC105369329, 15 more genes
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