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Items: 1 to 20 of 373

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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
    nsv5979686copy number variation1nstd209human GRCh38 chrX: 16,757,899-16,772,991 , GRCh37.p13 chrX: 16,776,022-16,791,114 RNU7-56P, SYAP1
    nsv5878717copy number variation1nstd209human GRCh38 chrX: 16,721,263-16,721,558 , GRCh37.p13 chrX: 16,739,386-16,739,681 SYAP1
    nsv5872627copy number variation1nstd209human GRCh38 chrX: 16,757,558-16,779,381 , GRCh37.p13 chrX: 16,775,681-16,797,504 SYAP1, RNU7-56P
    nsv5728676mobile element insertion1nstd211human GRCh38 chrX: 16,761,601-16,761,601 , GRCh37.p13 chrX: 16,779,724-16,779,724 SYAP1
    nsv5723391mobile element insertion1nstd211human GRCh38 chrX: 16,762,312-16,762,312 , GRCh37.p13 chrX: 16,780,435-16,780,435 SYAP1
    nsv5717033mobile element insertion1nstd211human GRCh38 chrX: 16,763,022-16,763,022 , GRCh37.p13 chrX: 16,781,145-16,781,145 SYAP1
    nsv5716256mobile element insertion1nstd211human GRCh38 chrX: 16,718,524-16,718,524 , GRCh37.p13 chrX: 16,736,647-16,736,647 SYAP1
    nsv5563293mobile element insertion1nstd206human GRCh38 chrX: 16,761,551-16,761,601 , GRCh37.p13 chrX: 16,779,674-16,779,724 SYAP1
    nsv5428189copy number variation1nstd206human GRCh38 chrX: 16,739,323-16,739,534 , GRCh37.p13 chrX: 16,757,446-16,757,657 SYAP1
    nsv5420882copy number variation1nstd206human GRCh38 chrX: 16,757,558-16,779,385 , GRCh37.p13 chrX: 16,775,681-16,797,508 SYAP1, RNU7-56P
    nsv5419062copy number variation1nstd206human GRCh38 chrX: 16,764,077-16,773,501 , GRCh37.p13 chrX: 16,782,200-16,791,624 SYAP1, RNU7-56P
    nsv5366439translocation1nstd200human GRCh38 chrX: 16,757,558-16,757,558 , GRCh38 chrX: 16,779,385-16,779,385 , GRCh37.p13 chrX: 16,797,508-16,797,508 , GRCh37.p13 chrX: 16,775,681-16,775,681 SYAP1
    nsv5195424mobile element insertion1nstd203human GRCh38 chrX: 16,763,337-16,763,366 , GRCh37.p13 chrX: 16,781,460-16,781,489 SYAP1
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv4905224copy number variation1nstd200human GRCh38 chrX: 16,722,332-16,729,044 , GRCh37.p13 chrX: 16,740,455-16,747,167 SYAP1
    nsv4781869copy number variation1nstd200human GRCh37 chrX: 16,775,681-16,797,508 , GRCh38.p12 chrX: 16,757,558-16,779,385 RNU7-56P, SYAP1
    nsv4779181copy number variation1nstd200human GRCh37 chrX: 16,769,495-16,771,247 , GRCh38.p12 chrX: 16,751,372-16,753,124 SYAP1
    nsv4769248copy number variation1nstd201human GRCh37 chrX: 168,546-21,870,371 , GRCh38.p12 chrX: 251,879-21,852,253 , AMELX, 248 more genes
    nsv4728486copy number variation1nstd102humanPathogenic GRCh37 chrX: 219,609-55,466,476 , GRCh38.p12 chrX: 302,942-55,440,043 CDK16, WASF4P, 772 more genes
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