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Items: 1 to 20 of 485

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148195copy number variation1nstd102humanPathogenic GRCh37 chr18: 63,476,940-77,960,815 , GRCh38.p12 chr18: 65,809,704-80,202,932 LOC105372202, LINC01896, 149 more genes
    nsv7137214copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,057,406-78,014,123 , GRCh38.p12 chr18: 68,390,169-80,256,240 LOC105372228, MIR548AV, 132 more genes
    nsv7137137copy number variation1nstd102humanPathogenic GRCh37 chr18: 71,740,696-78,005,231 , GRCh38.p12 chr18: 74,073,461-80,247,348 LOC339298, LOC105372201, 84 more genes
    nsv7099035copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,434,850-78,075,000 , GRCh38.p12 chr18: 68,767,613-80,259,271 LOC107985151, CD226, 129 more genes
    nsv7076595inversion1nstd229human GRCh38 chr18: 74,137,137-74,137,204 , GRCh37.p13 chr18: 71,804,372-71,804,439 FBXO15
    nsv7073685inversion1nstd229human GRCh38 chr18: 72,645,988-74,615,511 , GRCh37.p13 chr18: 70,313,223-72,282,747 LOC105372191, RN7SL551P, 19 more genes
    nsv7072261inversion1nstd229human GRCh38 chr18: 73,069,849-74,783,659 , GRCh37.p13 chr18: 70,737,084-72,495,615 TIMM21, CNDP2, 15 more genes
    nsv7016688copy number variation1nstd229human GRCh38 chr18: 74,146,233-74,146,337 , GRCh37.p13 chr18: 71,813,468-71,813,572 FBXO15
    nsv7015859copy number variation1nstd229human GRCh38 chr18: 74,123,893-74,131,872 , GRCh37.p13 chr18: 71,791,128-71,799,107 FBXO15
    nsv7014248copy number variation1nstd229human GRCh38 chr18: 74,082,801-74,086,800 , GRCh37.p13 chr18: 71,750,036-71,754,035 FBXO15
    nsv7013969copy number variation1nstd229human GRCh38 chr18: 74,079,801-74,209,600 , GRCh37.p13 chr18: 71,747,036-71,876,835 TIMM21, FBXO15
    nsv7012156copy number variation1nstd229human GRCh38 chr18: 73,615,032-74,455,029 , GRCh37.p13 chr18: 71,282,267-72,122,264 LINC01922, TIMM21, 9 more genes
    nsv7012145copy number variation1nstd229human GRCh38 chr18: 74,143,187-74,157,299 , GRCh37.p13 chr18: 71,810,422-71,824,534 FBXO15, TIMM21
    nsv7005298copy number variation1nstd229human GRCh38 chr18: 74,126,001-74,141,300 , GRCh37.p13 chr18: 71,793,236-71,808,535 FBXO15
    nsv7004892copy number variation1nstd229human GRCh38 chr18: 74,118,211-74,122,206 , GRCh37.p13 chr18: 71,785,446-71,789,441 FBXO15
    nsv7004366copy number variation1nstd229human GRCh38 chr18: 73,961,992-74,117,677 , GRCh37.p13 chr18: 71,629,227-71,784,912 FBXO15
    nsv7002981copy number variation1nstd229human GRCh38 chr18: 71,069,035-74,330,763 , GRCh37.p13 chr18: 68,736,271-71,997,998 MIR548AV, C18orf63, 24 more genes
    nsv7000270copy number variation1nstd229human GRCh38 chr18: 74,087,568-74,101,231 , GRCh37.p13 chr18: 71,754,803-71,768,466 FBXO15
    nsv7000104copy number variation1nstd229human GRCh38 chr18: 74,022,609-74,184,692 , GRCh37.p13 chr18: 71,689,844-71,851,927 TIMM21, FBXO15
    nsv6999456copy number variation1nstd229human GRCh38 chr18: 74,105,691-74,115,999 , GRCh37.p13 chr18: 71,772,926-71,783,234 FBXO15
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