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Items: 1 to 20 of 535

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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
    nsv5887525copy number variation1nstd209human GRCh38 chrX: 14,775,881-14,776,108 , GRCh37.p13 chrX: 14,794,003-14,794,230 FANCB
    nsv5884656copy number variation1nstd209human GRCh38 chrX: 14,779,641-14,781,285 , GRCh37.p13 chrX: 14,797,763-14,799,407 FANCB
    nsv5882073copy number variation1nstd209human GRCh38 chrX: 14,801,912-14,802,743 , GRCh37.p13 chrX: 14,820,034-14,820,865 FANCB
    nsv5873462copy number variation1nstd209human GRCh38 chrX: 14,699,820-14,699,869 , GRCh37.p13 chrX: 14,717,942-14,717,991 FANCB, GLRA2
    nsv5729104mobile element insertion2nstd211human GRCh38 chrX: 14,775,188-14,775,188 , GRCh37.p13 chrX: 14,793,310-14,793,310 FANCB
    nsv5717678mobile element insertion1nstd211human GRCh38 chrX: 14,693,062-14,693,062 , GRCh37.p13 chrX: 14,711,184-14,711,184 GLRA2, FANCB
    nsv5716989mobile element insertion1nstd211human GRCh38 chrX: 14,818,213-14,818,213 , GRCh37.p13 chrX: 14,836,335-14,836,335 FANCB
    nsv5672088copy number variation1nstd207human GRCh38 chrX: 14,779,641-14,781,285 , GRCh37.p13 chrX: 14,797,763-14,799,407 FANCB
    nsv5668337copy number variation1nstd207human GRCh38 chrX: 14,711,419-14,713,135 , GRCh37.p13 chrX: 14,729,541-14,731,257 GLRA2, FANCB
    nsv5665298inversion1nstd207human GRCh37.p13 chrX: 14,729,540-14,731,319 , GRCh38 chrX: 14,711,418-14,713,197 FANCB, GLRA2
    nsv5610395insertion1nstd207human GRCh38 chrX: 14,713,195-14,713,195 , GRCh37.p13 chrX: 14,731,317-14,731,317 GLRA2, FANCB
    nsv5559278mobile element insertion1nstd206human GRCh38 chrX: 14,818,213-14,818,262 , GRCh37.p13 chrX: 14,836,335-14,836,384 FANCB
    nsv5553786inversion1nstd206human GRCh38 chrX: 14,711,416-14,713,197 , GRCh37.p13 chrX: 14,729,538-14,731,319 FANCB, GLRA2
    nsv5431534copy number variation1nstd206human GRCh38 chrX: 14,869,700-14,869,781 , GRCh37.p13 chrX: 14,887,822-14,887,903 FANCB
    nsv5424874copy number variation1nstd206human GRCh38 chrX: 14,779,643-14,781,286 , GRCh37.p13 chrX: 14,797,765-14,799,408 FANCB
    nsv5424731copy number variation1nstd206human GRCh38 chrX: 14,775,889-14,776,109 , GRCh37.p13 chrX: 14,794,011-14,794,231 FANCB
    nsv5420174copy number variation1nstd206human GRCh38 chrX: 14,703,523-14,703,787 , GRCh37.p13 chrX: 14,721,645-14,721,909 GLRA2, FANCB
    nsv5415181copy number variation1nstd206human GRCh38 chrX: 14,831,837-14,838,078 , GRCh37.p13 chrX: 14,849,959-14,856,200 NPM1P9, FANCB
    nsv5366436translocation1nstd200human GRCh38 chrX: 14,869,781-14,869,781 , GRCh38 chrX: 14,869,700-14,869,700 , GRCh37.p13 chrX: 14,887,822-14,887,822 , GRCh37.p13 chrX: 14,887,903-14,887,903 FANCB
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