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Items: 1 to 20 of 452

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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
    nsv5878376copy number variation1nstd209human GRCh38 chrX: 24,470,806-24,595,189 , GRCh37.p13 chrX: 24,488,923-24,613,306 PCYT1B, SNRPEP9, 1 more genes
    nsv5877436copy number variation1nstd209human GRCh38 chrX: 24,593,374-24,593,470 , GRCh37.p13 chrX: 24,611,491-24,611,587 PCYT1B
    nsv5868082copy number variation1nstd209human GRCh38 chrX: 24,630,434-24,631,060 , GRCh37.p13 chrX: 24,648,551-24,649,177 H2BP7, PCYT1B
    nsv5723799mobile element insertion1nstd211human GRCh38 chrX: 24,593,484-24,593,484 , GRCh37.p13 chrX: 24,611,601-24,611,601 PCYT1B
    nsv5717546mobile element insertion1nstd211human GRCh38 chrX: 24,665,779-24,665,779 , GRCh37.p13 chrX: 24,683,896-24,683,896 PCYT1B
    nsv5611854insertion1nstd207human GRCh38 chrX: 24,611,105-24,611,105 , GRCh37.p13 chrX: 24,629,222-24,629,222 PCYT1B
    nsv5433029copy number variation1nstd206human GRCh38 chrX: 24,632,998-24,634,603 , GRCh37.p13 chrX: 24,651,115-24,652,720 H2BP7, PCYT1B
    nsv5429798copy number variation1nstd206human GRCh38 chrX: 24,580,706-24,582,103 , GRCh37.p13 chrX: 24,598,823-24,600,220 PCYT1B
    nsv5424202copy number variation1nstd206human GRCh38 chrX: 24,569,939-24,571,139 , GRCh37.p13 chrX: 24,588,056-24,589,256 PCYT1B
    nsv5416704copy number variation1nstd206human GRCh38 chrX: 24,630,434-24,631,061 , GRCh37.p13 chrX: 24,648,551-24,649,178 PCYT1B, H2BP7
    nsv5375968translocation1nstd200human GRCh38 chrX: 24,582,103-24,582,103 , GRCh38 chrX: 24,580,706-24,580,706 , GRCh37.p13 chrX: 24,598,823-24,598,823 , GRCh37.p13 chrX: 24,600,220-24,600,220 PCYT1B
    nsv5343327translocation1nstd200human GRCh37 chrX: 70,685,057-70,685,057 , GRCh37 chrX: 24,690,367-24,690,367 , GRCh38.p12 chrX: 24,672,250-24,672,250 , GRCh38.p12 chrX: 71,465,207-71,465,207 PCYT1B, TAF1
    nsv5195846mobile element insertion1nstd203human GRCh38 chrX: 24,646,422-24,646,435 , GRCh37.p13 chrX: 24,664,539-24,664,552 PCYT1B
    nsv5192082mobile element insertion1nstd203human GRCh38 chrX: 24,665,764-24,665,779 , GRCh37.p13 chrX: 24,683,881-24,683,896 PCYT1B
    nsv5190414mobile element insertion1nstd203human GRCh38 chrX: 24,665,769-24,665,779 , GRCh37.p13 chrX: 24,683,886-24,683,896 PCYT1B
    nsv5188807mobile element insertion1nstd203human GRCh38 chrX: 24,665,771-24,665,779 , GRCh37.p13 chrX: 24,683,888-24,683,896 PCYT1B
    nsv5181177mobile element insertion1nstd203human GRCh38 chrX: 24,609,612-24,609,631 , GRCh37.p13 chrX: 24,627,729-24,627,748 PCYT1B
    nsv5180415mobile element insertion1nstd203human GRCh38 chrX: 24,665,763-24,665,779 , GRCh37.p13 chrX: 24,683,880-24,683,896 PCYT1B
    nsv5178291mobile element insertion1nstd203human GRCh38 chrX: 24,601,609-24,601,624 , GRCh37.p13 chrX: 24,619,726-24,619,741 PCYT1B
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