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Items: 1 to 20 of 375

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5882744copy number variation1nstd209human GRCh38 chrX: 132,375,240-132,375,591 , GRCh37.p13 chrX: 131,509,268-131,509,619 MBNL3, RAP2C-AS1
    nsv5876868copy number variation1nstd209human GRCh38 chrX: 132,391,626-132,392,916 , GRCh37.p13 chrX: 131,525,654-131,526,944 RAP2C-AS1, MBNL3
    nsv5716834mobile element insertion1nstd211human GRCh38 chrX: 132,384,402-132,384,402 , GRCh37.p13 chrX: 131,518,430-131,518,430 RAP2C-AS1, MBNL3
    nsv5614532insertion1nstd207human GRCh38 chrX: 132,396,715-132,396,715 , GRCh37.p13 chrX: 131,530,743-131,530,743 RAP2C-AS1, MBNL3
    nsv5607306insertion1nstd207human GRCh38 chrX: 132,396,558-132,396,558 , GRCh37.p13 chrX: 131,530,586-131,530,586 MBNL3, RAP2C-AS1
    nsv5607129insertion1nstd207human GRCh38 chrX: 132,396,500-132,396,500 , GRCh37.p13 chrX: 131,530,528-131,530,528 RAP2C-AS1, MBNL3
    nsv5604671insertion1nstd207human GRCh38 chrX: 132,396,744-132,396,744 , GRCh37.p13 chrX: 131,530,772-131,530,772 MBNL3, RAP2C-AS1
    nsv5424501copy number variation1nstd206human GRCh38 chrX: 132,375,241-132,375,592 , GRCh37.p13 chrX: 131,509,269-131,509,620 MBNL3, RAP2C-AS1
    nsv5377072translocation1nstd200human GRCh38 chrX: 132,376,273-132,376,273 , GRCh38 chrX: 132,375,729-132,375,729 , GRCh37.p13 chrX: 131,509,757-131,509,757 , GRCh37.p13 chrX: 131,510,301-131,510,301 RAP2C-AS1, MBNL3
    nsv5196022mobile element insertion1nstd203human GRCh38 chrX: 132,384,385-132,384,402 , GRCh37.p13 chrX: 131,518,413-131,518,430 MBNL3, RAP2C-AS1
    nsv5195731mobile element insertion1nstd203human GRCh38 chrX: 132,449,487-132,449,487 , GRCh37.p13 chrX: 131,583,515-131,583,515 MBNL3
    nsv5168487mobile element insertion1nstd203human GRCh38 chrX: 132,464,537-132,464,552 , GRCh37.p13 chrX: 131,598,565-131,598,580 MBNL3
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv4909150copy number variation1nstd200human GRCh38 chrX: 131,985,692-132,852,923 , GRCh37.p13 chrX: 131,119,720-131,986,951 STK26, RAP2C, 7 more genes
    nsv4782347copy number variation1nstd200human GRCh37 chrX: 131,119,720-131,986,951 , GRCh38.p12 chrX: 131,985,692-132,852,923 RAP2C, AGKP2, 7 more genes
    nsv4780451copy number variation1nstd200human GRCh37 chrX: 131,556,937-131,557,147 , GRCh38.p12 chrX: 132,422,909-132,423,119 RAP2C-AS1, MBNL3
    nsv4780450copy number variation1nstd200human GRCh37 chrX: 131,509,757-131,510,301 , GRCh38.p12 chrX: 132,375,729-132,376,273 RAP2C-AS1, MBNL3
    nsv4780449copy number variation1nstd200human GRCh37 chrX: 131,509,269-131,509,620 , GRCh38.p12 chrX: 132,375,241-132,375,592 RAP2C-AS1, MBNL3
    nsv4769250copy number variation1nstd201human GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579 , AGTR2, 959 more genes
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