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Items: 1 to 20 of 736

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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
    nsv6131714mobile element insertion1nstd186human GRCh37 chrX: 111,557,758-111,557,809 , GRCh38.p12 chrX: 112,314,530-112,314,581 RTL4
    nsv6125198insertion1nstd186human GRCh37 chrX: 111,374,208-111,374,246 , GRCh38.p12 chrX: 112,130,980-112,131,018 RTL4
    nsv6125188insertion1nstd186human GRCh37 chrX: 111,662,822-111,662,822 , GRCh38.p12 chrX: 112,419,594-112,419,594 RTL4
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5972806inversion1nstd209human GRCh38 chrX: 112,447,795-112,447,885 , GRCh37.p13 chrX: 111,691,023-111,691,113 RTL4
    nsv5959405insertion1nstd209human GRCh38 chrX: 112,419,611-112,419,611 , GRCh37.p13 chrX: 111,662,839-111,662,839 RTL4
    nsv5954029insertion1nstd209human GRCh38 chrX: 112,314,521-112,314,521 , GRCh37.p13 chrX: 111,557,749-111,557,749 RTL4
    nsv5949769insertion1nstd209human GRCh38 chrX: 112,130,967-112,130,967 , GRCh37.p13 chrX: 111,374,195-111,374,195 RTL4
    nsv5882130copy number variation1nstd209human GRCh38 chrX: 112,376,740-112,378,550 , GRCh37.p13 chrX: 111,619,968-111,621,778 RTL4
    nsv5874855copy number variation1nstd209human GRCh38 chrX: 112,160,837-112,160,891 , GRCh37.p13 chrX: 111,404,065-111,404,119 RTL4
    nsv5730967mobile element insertion2nstd211human GRCh38 chrX: 112,446,090-112,446,090 , GRCh37.p13 chrX: 111,689,318-111,689,318 RTL4
    nsv5729032mobile element insertion1nstd211human GRCh38 chrX: 112,388,038-112,388,038 , GRCh37.p13 chrX: 111,631,266-111,631,266 RTL4
    nsv5723293mobile element insertion1nstd211human GRCh38 chrX: 112,098,844-112,098,844 , GRCh37.p13 chrX: 111,342,072-111,342,072 RTL4
    nsv5723087mobile element insertion1nstd211human GRCh38 chrX: 112,371,397-112,371,397 , GRCh37.p13 chrX: 111,614,625-111,614,625 RTL4
    nsv5719719mobile element insertion1nstd211human GRCh38 chrX: 112,304,033-112,304,033 , GRCh37.p13 chrX: 111,547,261-111,547,261 RTL4
    nsv5715627mobile element insertion1nstd211human GRCh38 chrX: 112,177,784-112,177,784 , GRCh37.p13 chrX: 111,421,012-111,421,012 RTL4
    nsv5715386mobile element insertion2nstd211human GRCh38 chrX: 112,314,530-112,314,530 , GRCh37.p13 chrX: 111,557,758-111,557,758 RTL4
    nsv5715182mobile element insertion1nstd211human GRCh38 chrX: 112,236,462-112,236,462 , GRCh37.p13 chrX: 111,479,690-111,479,690 RTL4
    nsv5670227copy number variation1nstd207human GRCh38 chrX: 112,236,398-112,236,469 , GRCh37.p13 chrX: 111,479,626-111,479,697 RTL4
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