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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072209inversion1nstd229human GRCh38 chr8: 144,433,363-144,843,412 , GRCh37.p13 chr8: 145,659,902-146,068,797 ZNF517, RN7SL395P, 26 more genes
    nsv6874383copy number variation1nstd229human GRCh38 chr8: 144,779,691-144,785,807 , GRCh37.p13 chr8: 146,005,076-146,011,192 RN7SL395P, ZNF34
    nsv6873736copy number variation1nstd229human GRCh38 chr8: 144,766,717-145,025,810 , GRCh37.p13 chr8: 145,992,102-146,251,196 RPL8, LOC105375805, 12 more genes
    nsv6873542copy number variation1nstd229human GRCh38 chr8: 144,315,680-144,852,644 , GRCh37.p13 chr8: 145,659,902-146,078,029 FBXL6, MIR6848, 40 more genes
    nsv6873432copy number variation1nstd229human GRCh38 chr8: 144,780,114-144,783,155 , GRCh37.p13 chr8: 146,005,499-146,008,540 ZNF34
    nsv6860894copy number variation1nstd229human GRCh38 chr8: 144,765,623-144,777,368 , GRCh37.p13 chr8: 145,991,008-146,002,753 ZNF34, LOC105375805
    nsv6637599copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,899,733-146,107,871 , GRCh38.p12 chr8: 144,674,348-144,882,486 LOC107986986, LOC100130027, 12 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6558782inversion1nstd223human GRCh38 chr8: 143,001,224-145,028,420 , GRCh37.p13 chr8: 144,082,641-146,253,806 ZFP41, LY6H, 118 more genes
    nsv6557281inversion1nstd223human GRCh38 chr8: 144,781,098-144,781,419 , GRCh37.p13 chr8: 146,006,483-146,006,804 ZNF34
    nsv6429650copy number variation1nstd223human GRCh38 chr8: 144,687,575-144,884,662 , GRCh37.p13 chr8: 145,912,960-146,110,047 MIR6850, ZNF7, 12 more genes
    nsv6428290copy number variation1nstd223human GRCh38 chr8: 144,784,954-144,786,737 , GRCh37.p13 chr8: 146,010,339-146,012,122 RN7SL395P, ZNF34
    nsv6426730copy number variation1nstd223human GRCh38 chr8: 144,765,622-144,777,367 , GRCh37.p13 chr8: 145,991,007-146,002,752 LOC105375805, ZNF34
    nsv6426641copy number variation1nstd223human GRCh38 chr8: 144,780,113-144,783,154 , GRCh37.p13 chr8: 146,005,498-146,008,539 ZNF34
    nsv6416302copy number variation1nstd223human GRCh38 chr8: 144,782,700-144,784,005 , GRCh37.p13 chr8: 146,008,085-146,009,390 RN7SL395P, ZNF34
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6313487copy number variation1nstd102humanPathogenic GRCh37 chr8: 130,863,093-146,295,771 , GRCh38.p12 chr8: 129,850,847-145,070,385 LOC105375784, CYP11B2, 253 more genes
    nsv6291044copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,921,005-146,295,771 , GRCh38.p12 chr8: 144,695,620-145,070,385 LOC100996662, ZNF34, 18 more genes
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