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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5910560copy number variation1nstd209human GRCh38 chr10: 88,998,748-88,998,866 , GRCh37.p13 chr10: 90,758,505-90,758,623 FAS
    nsv5853829copy number variation1nstd209human GRCh38 chr10: 88,990,222-88,992,321 , GRCh37.p13 chr10: 90,749,979-90,752,078 ACTA2, FAS, 1 more genes
    nsv5727156mobile element insertion1nstd211human GRCh38 chr10: 89,005,196-89,005,196 , GRCh37.p13 chr10: 90,764,953-90,764,953 FAS
    nsv5711407mobile element insertion1nstd211human GRCh38 chr10: 88,999,197-88,999,197 , GRCh37.p13 chr10: 90,758,954-90,758,954 FAS
    nsv5698277mobile element insertion2nstd211human GRCh38 chr10: 88,980,189-88,980,189 , GRCh37.p13 chr10: 90,739,946-90,739,946 FAS, ACTA2
    nsv5553242insertion1nstd206human GRCh38 chr10: 88,999,873-88,999,877 , GRCh37.p13 chr10: 90,759,630-90,759,634 FAS
    nsv5484654copy number variation1nstd206human GRCh38 chr10: 88,357,217-89,008,458 , GRCh37.p13 chr10: 90,116,974-90,768,215 , RCBTB2P1, 17 more genes
    nsv5411510mobile element insertion1nstd206human GRCh38 chr10: 88,980,189-88,980,240 , GRCh37.p13 chr10: 90,739,946-90,739,997 FAS, ACTA2
    nsv5199794mobile element insertion1nstd203human GRCh38 chr10: 88,972,523-88,972,523 , GRCh37.p13 chr10: 90,732,280-90,732,280 ACTA2, FAS
    nsv5138119mobile element insertion1nstd203human GRCh38 chr10: 88,976,013-88,976,026 , GRCh37.p13 chr10: 90,735,770-90,735,783 ACTA2, FAS
    nsv5133876mobile element insertion1nstd203human GRCh38 chr10: 88,982,323-88,982,336 , GRCh37.p13 chr10: 90,742,080-90,742,093 FAS, ACTA2
    nsv5133377mobile element insertion1nstd203human GRCh38 chr10: 88,980,172-88,980,189 , GRCh37.p13 chr10: 90,739,929-90,739,946 ACTA2, FAS
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4986557copy number variation1nstd200human GRCh38 chr10: 88,982,741-88,984,047 , GRCh37.p13 chr10: 90,742,498-90,743,804 FAS, ACTA2
    nsv4838940copy number variation1nstd200human GRCh37 chr10: 90,116,974-90,768,215 , GRCh38.p12 chr10: 88,357,217-89,008,458 , RNLS, 17 more genes
    nsv4764591insertion1nstd199human GRCh37 chr10: 90,739,936-90,739,936 , GRCh38.p12 chr10: 88,980,179-88,980,179 ACTA2, FAS
    nsv4729624copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,685,387-92,144,296 , GRCh38.p12 chr10: 86,925,630-90,384,539 LOC105378414, RN7SL78P, 84 more genes
    nsv4728982copy number variation1nstd102humanUncertain significance GRCh37 chr10: 90,122,675-90,771,228 , GRCh38.p12 chr10: 88,362,918-89,011,471 LIPJ, PTCD2P2, 16 more genes
    nsv4682162copy number variation1nstd102humanPathogenic GRCh37 chr10: 90,530,602-91,087,835 , GRCh38.p12 chr10: 88,770,845-89,328,078 MIR4679-2, ACTA2-AS1, 17 more genes
    nsv4681215copy number variation1nstd102humanPathogenic GRCh37 chr10: 90,749,256-91,007,425 , GRCh38.p12 chr10: 88,989,499-89,247,668 ACTA2, FAS, 7 more genes
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