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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 more genes
    nsv6123760insertion1nstd186human GRCh37 chrX: 109,948,668-109,948,710 , GRCh38.p12 chrX: 110,705,440-110,705,482 CHRDL1
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5874902copy number variation1nstd209human GRCh38 chrX: 110,689,398-110,689,798 , GRCh37.p13 chrX: 109,932,626-109,933,026 CHRDL1
    nsv5874779copy number variation1nstd209human GRCh38 chrX: 110,695,373-110,698,910 , GRCh37.p13 chrX: 109,938,601-109,942,138 CHRDL1
    nsv5730551mobile element insertion1nstd211human GRCh38 chrX: 110,689,949-110,689,949 , GRCh37.p13 chrX: 109,933,177-109,933,177 CHRDL1
    nsv5726004mobile element insertion1nstd211human GRCh38 chrX: 110,689,905-110,689,905 , GRCh37.p13 chrX: 109,933,133-109,933,133 CHRDL1
    nsv5718505mobile element insertion1nstd211human GRCh38 chrX: 110,712,523-110,712,523 , GRCh37.p13 chrX: 109,955,751-109,955,751 CHRDL1
    nsv5665422copy number variation1nstd207human GRCh38 chrX: 110,689,456-110,689,515 , GRCh37.p13 chrX: 109,932,684-109,932,743 CHRDL1
    nsv5621432insertion1nstd207human GRCh38 chrX: 110,689,057-110,689,057 , GRCh37.p13 chrX: 109,932,285-109,932,285 CHRDL1
    nsv5617270insertion1nstd207human GRCh38 chrX: 110,705,431-110,705,431 , GRCh37.p13 chrX: 109,948,659-109,948,659 CHRDL1
    nsv5611742insertion1nstd207human GRCh38 chrX: 110,689,572-110,689,572 , GRCh37.p13 chrX: 109,932,800-109,932,800 CHRDL1
    nsv5611639insertion1nstd207human GRCh38 chrX: 110,689,951-110,689,951 , GRCh37.p13 chrX: 109,933,179-109,933,179 CHRDL1
    nsv5545368insertion1nstd206human GRCh38 chrX: 110,741,228-110,741,228 , GRCh37.p13 chrX: 109,984,456-109,984,456 CHRDL1
    nsv5543270insertion1nstd206human GRCh38 chrX: 110,705,440-110,705,482 , GRCh37.p13 chrX: 109,948,668-109,948,710 CHRDL1
    nsv5431269copy number variation1nstd206human GRCh38 chrX: 110,695,374-110,698,911 , GRCh37.p13 chrX: 109,938,602-109,942,139 CHRDL1
    nsv5419709copy number variation1nstd206human GRCh38 chrX: 110,711,977-110,713,049 , GRCh37.p13 chrX: 109,955,205-109,956,277 CHRDL1
    nsv5383104copy number variation1nstd186human GRCh37 chrX: 109,938,602-109,942,139 , GRCh38.p12 chrX: 110,695,374-110,698,911 CHRDL1
    nsv5376872translocation1nstd200human GRCh38 chrX: 110,738,638-110,738,638 , GRCh38 chrX: 110,741,236-110,741,236 , GRCh37.p13 chrX: 109,984,464-109,984,464 , GRCh37.p13 chrX: 109,981,866-109,981,866 CHRDL1
    nsv5376871translocation1nstd200human GRCh38 chrX: 110,741,228-110,741,228 , GRCh38 chrX: 110,738,210-110,738,210 , GRCh37.p13 chrX: 109,984,456-109,984,456 , GRCh37.p13 chrX: 109,981,438-109,981,438 CHRDL1
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