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Items: 1 to 20 of 199

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5491842copy number variation1nstd206human GRCh38 chr8: 142,196,282-142,337,354 , GRCh37.p13 chr8: 143,277,643-143,418,715 , TSNARE1, 3 more genes
    nsv5307207copy number variation1nstd204human GRCh38.p13 chr8: 142,204,820-142,230,560 , GRCh37.p13 chr8: 143,286,181-143,311,921 , TSNARE1, 1 more genes
    nsv5254269copy number variation1nstd204human GRCh37.p13 chr8: 142,920,862-143,323,661 , GRCh38.p13 chr8: 141,839,501-142,242,300 , TSNARE1, 4 more genes
    nsv5249951copy number variation1nstd204human GRCh38.p13 chr8: 142,204,711-142,230,391 , GRCh37.p13 chr8: 143,286,072-143,311,752 , LINC00051, 1 more genes
    nsv4969145copy number variation1nstd200human GRCh38 chr8: 142,157,233-142,398,503 , GRCh37.p13 chr8: 143,238,594-143,479,864 , TSNARE1, 4 more genes
    nsv4829362copy number variation1nstd200human GRCh37 chr8: 143,286,190-143,311,913 , GRCh38.p12 chr8: 142,204,829-142,230,552 , LINC00051, 1 more genes
    nsv4675664copy number variation1nstd102humanPathogenic GRCh37 chr8: 128,877,995-146,295,771 , GRCh38.p12 chr8: 127,865,749-145,070,385 LOC105375789, LINC02990, 270 more genes
    nsv4675273copy number variation1nstd102humanPathogenic GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385 TOP1MT, SLA, 379 more genes
    nsv4675029copy number variation1nstd102humanPathogenic GRCh37 chr8: 142,132,678-145,569,441 , GRCh38.p12 chr8: 141,122,579-144,345,779 RHPN1-AS1, MIR6847, 117 more genes
    nsv4674996copy number variation1nstd102humanPathogenic GRCh37 chr8: 126,892,814-143,750,028 , GRCh38.p12 chr8: 125,880,570-142,668,610 POU5F1B, DNAJC8P3, 158 more genes
    nsv4457078copy number variation1nstd102humanPathogenic GRCh37 chr8: 139,188,797-146,295,771 , GRCh38.p12 chr8: 138,176,554-145,070,385 GSDMD, MROH1, 181 more genes
    nsv4456997copy number variation1nstd102humanPathogenic GRCh37 chr8: 125,496,223-146,295,771 , GRCh38.p12 chr8: 124,483,982-145,070,385 LOC107986906, GPIHBP1, 317 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4456783copy number variation1nstd102humanPathogenic GRCh37 chr8: 122,193,546-146,295,771 , GRCh38.p12 chr8: 121,181,306-145,070,385 HAS2, ZNF696, 369 more genes
    nsv4456083copy number variation1nstd102humanUncertain significance GRCh37 chr8: 142,988,974-144,218,537 , GRCh38.p12 chr8: 141,907,613-143,137,120 LY6E, CYP11B2, 32 more genes
    nsv4455524copy number variation1nstd102humanPathogenic GRCh37 chr8: 136,059,859-146,295,771 , GRCh38.p12 chr8: 135,047,616-145,070,385 LINC00051, LOC107986982, 197 more genes
    nsv4399968copy number variation1nstd174human GRCh37 chr8: 143,136,801-144,016,864 , GRCh38.p12 chr8: 142,055,440-142,935,448 , RN7SL260P, 24 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4331387inversion1nstd166human GRCh37.p13 chr8: 142,092,526-144,206,149 , GRCh38.p12 chr8: 141,082,427-143,124,732 , ADGRB1, 49 more genes
    nsv3966223insertion1nstd168human GRCh38 chr8: 142,145,323-142,292,758 , GRCh37.p13 chr8: 143,226,684-143,374,119 , TSNARE1, 4 more genes
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