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Items: 1 to 20 of 772

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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
    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
    nsv7073943inversion1nstd229human GRCh38 chr18: 73,206,000-73,214,622 , GRCh37.p13 chr18: 70,873,235-70,881,857 LINC02864
    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
    nsv7070589inversion1nstd229human GRCh38 chr18: 72,525,979-73,914,311 , GRCh37.p13 chr18: 70,193,214-71,581,546 RNA5SP460, MIR548AV, 9 more genes
    nsv7068944inversion1nstd229human GRCh38 chr18: 73,214,018-73,219,085 , GRCh37.p13 chr18: 70,881,253-70,886,320 LINC02864
    nsv7017603copy number variation1nstd229human GRCh38 chr18: 72,958,001-73,291,800 , GRCh37.p13 chr18: 70,625,236-70,959,035 LINC02864
    nsv7017086copy number variation1nstd229human GRCh38 chr18: 73,257,328-73,260,648 , GRCh37.p13 chr18: 70,924,563-70,927,883 LINC02864
    nsv7015421copy number variation1nstd229human GRCh38 chr18: 73,245,901-73,287,000 , GRCh37.p13 chr18: 70,913,136-70,954,235 LINC02864
    nsv7013343copy number variation1nstd229human GRCh38 chr18: 73,165,301-73,168,900 , GRCh37.p13 chr18: 70,832,536-70,836,135 LINC02864
    nsv7012679copy number variation1nstd229human GRCh38 chr18: 73,045,809-73,601,745 , GRCh37.p13 chr18: 70,713,044-71,268,980 LINC02864, LINC02582
    nsv7012121copy number variation1nstd229human GRCh38 chr18: 73,245,051-73,323,291 , GRCh37.p13 chr18: 70,912,286-70,990,526 LINC02864, LINC02582
    nsv7011895copy number variation1nstd229human GRCh38 chr18: 73,236,638-73,388,800 , GRCh37.p13 chr18: 70,903,873-71,056,035 LINC02864, LINC02582
    nsv7011429copy number variation1nstd229human GRCh38 chr18: 73,254,297-73,259,945 , GRCh37.p13 chr18: 70,921,532-70,927,180 LINC02864
    nsv7011112copy number variation1nstd229human GRCh38 chr18: 73,239,328-73,239,360 , GRCh37.p13 chr18: 70,906,563-70,906,595 LINC02864
    nsv7010901copy number variation1nstd229human GRCh38 chr18: 73,189,401-73,198,700 , GRCh37.p13 chr18: 70,856,636-70,865,935 LINC02864
    nsv7008168copy number variation1nstd229human GRCh38 chr18: 73,197,431-73,266,256 , GRCh37.p13 chr18: 70,864,666-70,933,491 LINC02864
    nsv7005830copy number variation1nstd229human GRCh38 chr18: 73,179,020-73,179,090 , GRCh37.p13 chr18: 70,846,255-70,846,325 LINC02864
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