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Items: 1 to 20 of 239

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926960copy number variation1nstd209human GRCh38 chr11: 74,237,006-74,237,167 , GRCh37.p13 chr11: 73,948,051-73,948,212 PPME1
    nsv5720408mobile element insertion2nstd211human GRCh38 chr11: 74,240,116-74,240,116 , GRCh37.p13 chr11: 73,951,161-73,951,161 PPME1
    nsv5713120mobile element insertion2nstd211human GRCh38 chr11: 74,229,492-74,229,492 , GRCh37.p13 chr11: 73,940,537-73,940,537 PPME1
    nsv5711746mobile element insertion1nstd211human GRCh38 chr11: 74,196,073-74,196,073 , GRCh37.p13 chr11: 73,907,118-73,907,118 PPME1
    nsv5709131mobile element insertion1nstd211human GRCh38 chr11: 74,196,084-74,196,084 , GRCh37.p13 chr11: 73,907,129-73,907,129 PPME1
    nsv5645879insertion1nstd207human GRCh38 chr11: 74,229,477-74,229,477 , GRCh37.p13 chr11: 73,940,522-73,940,522 PPME1
    nsv5558719mobile element insertion1nstd206human GRCh38 chr11: 74,240,116-74,240,167 , GRCh37.p13 chr11: 73,951,161-73,951,212 PPME1
    nsv5511249copy number variation1nstd206human GRCh38 chr11: 74,247,818-74,247,900 , GRCh37.p13 chr11: 73,958,863-73,958,945 PPME1
    nsv5510375copy number variation1nstd206human GRCh38 chr11: 74,170,227-74,170,670 , GRCh37.p13 chr11: 73,881,272-73,881,715 PPME1, C2CD3
    nsv5501333copy number variation1nstd206human GRCh38 chr11: 74,181,284-74,182,526 , GRCh37.p13 chr11: 73,892,329-73,893,571 PPME1
    nsv5498419copy number variation1nstd206human GRCh38 chr11: 74,195,696-74,201,000 , GRCh37.p13 chr11: 73,906,741-73,912,045 PPME1, RNA5SP343
    nsv5497882copy number variation1nstd206human GRCh38 chr11: 74,237,009-74,237,168 , GRCh37.p13 chr11: 73,948,054-73,948,213 PPME1
    nsv5494028copy number variation1nstd206human GRCh38 chr11: 74,225,600-74,828,943 , GRCh37.p13 chr11: 73,936,645-74,539,988 RNF169, MIR4696, 19 more genes
    nsv5410260mobile element insertion1nstd206human GRCh38 chr11: 74,229,492-74,229,543 , GRCh37.p13 chr11: 73,940,537-73,940,588 PPME1
    nsv5396979mobile element insertion1nstd206human GRCh38 chr11: 74,196,084-74,196,132 , GRCh37.p13 chr11: 73,907,129-73,907,177 PPME1
    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
    nsv5373716translocation1nstd200human GRCh38 chr11: 74,169,754-74,169,754 , GRCh38 chr11: 74,175,261-74,175,261 , GRCh37.p13 chr11: 73,880,799-73,880,799 , GRCh37.p13 chr11: 73,886,306-73,886,306 C2CD3, PPME1
    nsv5355369translocation1nstd200human GRCh38 chr11: 74,237,168-74,237,168 , GRCh38 chr11: 74,237,009-74,237,009 , GRCh37.p13 chr11: 73,948,213-73,948,213 , GRCh37.p13 chr11: 73,948,054-73,948,054 PPME1
    nsv5355368translocation1nstd200human GRCh38 chr11: 74,170,670-74,170,670 , GRCh38 chr11: 74,170,227-74,170,227 , GRCh37.p13 chr11: 73,881,715-73,881,715 , GRCh37.p13 chr11: 73,881,272-73,881,272 C2CD3, PPME1
    nsv5338944translocation1nstd200human GRCh37 chr11: 73,881,272-73,881,272 , GRCh37 chr11: 73,881,715-73,881,715 , GRCh38.p12 chr11: 74,170,227-74,170,227 , GRCh38.p12 chr11: 74,170,670-74,170,670 C2CD3, PPME1
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