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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv5956993insertion1nstd209human GRCh38 chr1: 19,175,319-19,175,319 , GRCh37.p13 chr1: 19,501,813-19,501,813 UBR4
    nsv5951839insertion1nstd209human GRCh38 chr1: 19,118,592-19,118,592 , GRCh37.p13 chr1: 19,445,086-19,445,086 UBR4
    nsv5951290insertion1nstd209human GRCh38 chr1: 19,190,312-19,190,312 , GRCh37.p13 chr1: 19,516,806-19,516,806 UBR4
    nsv5949126insertion1nstd209human GRCh38 chr1: 19,159,895-19,159,895 , GRCh37.p13 chr1: 19,486,389-19,486,389 UBR4
    nsv5877582copy number variation1nstd209human GRCh38 chr1: 19,212,768-19,276,163 , GRCh37.p13 chr1: 19,539,262-19,602,657 AKR7A3, EMC1, 4 more genes
    nsv5874151copy number variation1nstd209human GRCh38 chr1: 13,714,112-20,623,728 , GRCh37.p13 chr1: 14,040,607-20,950,221 , TRV-CAC11-1, 171 more genes
    nsv5869137copy number variation1nstd209human GRCh38 chr1: 19,189,137-19,189,241 , GRCh37.p13 chr1: 19,515,631-19,515,735 UBR4
    nsv5828796copy number variation1nstd209human GRCh38 chr1: 19,212,588-19,234,758 , GRCh37.p13 chr1: 19,539,082-19,561,252 EMC1, EMC1-AS1, 1 more genes
    nsv5693177mobile element insertion2nstd211human GRCh38 chr1: 19,159,911-19,159,911 , GRCh37.p13 chr1: 19,486,405-19,486,405 UBR4
    nsv5677588mobile element insertion2nstd211human GRCh38 chr1: 19,132,625-19,132,625 , GRCh37.p13 chr1: 19,459,119-19,459,119 UBR4
    nsv5543007insertion1nstd206human GRCh38 chr1: 19,118,606-19,118,643 , GRCh37.p13 chr1: 19,445,100-19,445,137 UBR4
    nsv5430373copy number variation1nstd206human GRCh38 chr1: 19,092,425-19,092,489 , GRCh37.p13 chr1: 19,418,919-19,418,983 UBR4
    nsv5429799copy number variation1nstd206human GRCh38 chr1: 19,079,159-19,079,238 , GRCh37.p13 chr1: 19,405,653-19,405,732 UBR4
    nsv5420517copy number variation1nstd206human GRCh38 chr1: 19,189,137-19,189,242 , GRCh37.p13 chr1: 19,515,631-19,515,736 UBR4
    nsv5401711mobile element insertion1nstd206human GRCh38 chr1: 19,159,911-19,159,962 , GRCh37.p13 chr1: 19,486,405-19,486,456 UBR4
    nsv5381289copy number variation1nstd102humanUncertain significance GRCh37 chr1: 19,433,063-19,547,342 , GRCh38.p12 chr1: 19,106,569-19,220,848 EMC1-AS1, EMC1, 1 more genes
    nsv5356557translocation1nstd200human GRCh38 chr9: 113,042,497-113,042,497 , GRCh38 chr1: 19,175,321-19,175,321 , GRCh37.p13 chr1: 19,501,815-19,501,815 , GRCh37.p13 chr9: 115,804,777-115,804,777 ZFP37, UBR4
    nsv5334599translocation1nstd200human GRCh37 chr1: 19,405,732-19,405,732 , GRCh37 chr1: 19,405,653-19,405,653 , GRCh38.p12 chr1: 19,079,238-19,079,238 , GRCh38.p12 chr1: 19,079,159-19,079,159 UBR4
    nsv5330660translocation1nstd200human GRCh37 chr9: 115,804,777-115,804,777 , GRCh37 chr1: 19,501,815-19,501,815 , GRCh38.p12 chr1: 19,175,321-19,175,321 , GRCh38.p12 chr9: 113,042,497-113,042,497 ZFP37, UBR4
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