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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130537insertion1nstd186human GRCh37 chr15: 98,628,078-98,628,078 , GRCh38.p12 chr15: 98,084,849-98,084,849 LINC01582
    nsv6112780copy number variation1nstd102humanPathogenic GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538 LOC105371009, ST8SIA2, 149 more genes
    nsv5973246inversion1nstd209human GRCh38 chr15: 97,535,582-101,746,493 , GRCh37.p13 chr15: 98,078,812-102,286,696 , ALDH1A3, 71 more genes
    nsv5970442insertion1nstd209human GRCh38 chr15: 98,084,855-98,084,855 , GRCh37.p13 chr15: 98,628,084-98,628,084 LINC01582
    nsv5944101copy number variation1nstd209human GRCh38 chr15: 98,082,612-98,084,863 , GRCh37.p13 chr15: 98,625,841-98,628,092 LINC01582
    nsv5939025copy number variation1nstd209human GRCh38 chr15: 98,082,528-98,082,639 , GRCh37.p13 chr15: 98,625,757-98,625,868 LINC01582
    nsv5884419copy number variation1nstd209human GRCh38 chr15: 98,082,835-98,085,438 , GRCh37.p13 chr15: 98,626,064-98,628,667 LINC01582
    nsv5871826copy number variation1nstd209human GRCh38 chr15: 98,086,286-98,087,749 , GRCh37.p13 chr15: 98,629,515-98,630,978 LINC01582
    nsv5657280insertion1nstd207human GRCh38 chr15: 98,084,849-98,084,849 , GRCh37.p13 chr15: 98,628,078-98,628,078 LINC01582
    nsv5546431insertion1nstd206human GRCh38 chr15: 98,084,849-98,084,849 , GRCh37.p13 chr15: 98,628,078-98,628,078 LINC01582
    nsv5527619copy number variation1nstd206human GRCh38 chr15: 98,086,312-98,100,229 , GRCh37.p13 chr15: 98,629,541-98,643,458 LINC01582
    nsv5009237copy number variation1nstd200human GRCh38 chr15: 98,086,312-98,100,229 , GRCh37.p13 chr15: 98,629,541-98,643,458 LINC01582
    nsv5002653copy number variation1nstd200human GRCh38 chr15: 97,992,912-98,170,283 , GRCh37.p13 chr15: 98,536,142-98,713,512 LINC01582, LINC02251, 3 more genes
    nsv4854263copy number variation1nstd200human GRCh37 chr15: 98,629,541-98,643,458 , GRCh38.p12 chr15: 98,086,312-98,100,229 LINC01582
    nsv4750652insertion1nstd199human GRCh37 chr15: 98,628,052-98,628,052 , GRCh38.p12 chr15: 98,084,823-98,084,823 LINC01582
    nsv4729102copy number variation1nstd102humanPathogenic GRCh37 chr15: 98,275,761-102,358,202 , GRCh38.p12 chr15: 97,732,531-101,817,999 LOC105371009, ALDH1A3-AS1, 71 more genes
    nsv4729097copy number variation1nstd102humanUncertain significance GRCh37 chr15: 97,967,733-98,665,757 , GRCh38.p12 chr15: 97,424,503-98,122,528 LOC105371010, ARRDC4, 10 more genes
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4675839copy number variation1nstd102humanUncertain significance GRCh37 chr15: 97,242,441-98,823,437 , GRCh38.p12 chr15: 96,699,211-98,280,208 SPATA8-AS1, LOC105371002, 19 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
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