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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098605copy number variation1nstd102humanUncertain significance GRCh37 chrX: 15,580,028-15,864,154 , GRCh38.p12 chrX: 15,561,905-15,846,031 ACE2, CA5BP1, 8 more genes
    nsv7098592copy number variation3nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 14,861,689-15,870,650 , GRCh38.p12 chrX: 14,843,567-15,852,527 VEGFD, CA5BP1-CA5B, 20 more genes
    nsv7085717copy number variation1nstd229human GRCh38 chrX: 15,782,749-15,782,876 , GRCh37.p13 chrX: 15,800,872-15,800,999 CA5B, CA5BP1-CA5B
    nsv7085716copy number variation1nstd229human GRCh38 chrX: 15,775,828-15,775,906 , GRCh37.p13 chrX: 15,793,951-15,794,029 CA5BP1-CA5B, CA5B
    nsv7085715copy number variation1nstd229human GRCh38 chrX: 15,758,347-15,763,894 , GRCh37.p13 chrX: 15,776,470-15,782,017 CA5BP1-CA5B, CA5B
    nsv7085714copy number variation1nstd229human GRCh38 chrX: 15,739,552-15,742,321 , GRCh37.p13 chrX: 15,757,675-15,760,444 CA5B, CA5BP1-CA5B
    nsv7085713copy number variation1nstd229human GRCh38 chrX: 15,691,663-16,185,760 , GRCh37.p13 chrX: 15,709,786-16,203,883 INE2, CA5BP1-CA5B, 8 more genes
    nsv7085711copy number variation1nstd229human GRCh38 chrX: 15,683,835-15,749,525 , GRCh37.p13 chrX: 15,701,958-15,767,648 CA5BP1-CA5B, CA5BP1, 1 more genes
    nsv7085709copy number variation1nstd229human GRCh38 chrX: 15,656,438-16,128,491 , GRCh37.p13 chrX: 15,674,561-16,146,614 CA5BP1, SETP15, 8 more genes
    nsv7085708copy number variation1nstd229human GRCh38 chrX: 15,639,401-15,863,200 , GRCh37.p13 chrX: 15,657,524-15,881,323 INE2, ZRSR2, 6 more genes
    nsv7085700copy number variation1nstd229human GRCh38 chrX: 15,599,210-15,766,074 , GRCh37.p13 chrX: 15,617,333-15,784,197 PTMAP14, CA5B, 5 more genes
    nsv7085699copy number variation1nstd229human GRCh38 chrX: 15,591,291-16,152,449 , GRCh37.p13 chrX: 15,609,414-16,170,572 CA5BP1-CA5B, ACE2-DT, 11 more genes
    nsv7085698copy number variation1nstd229human GRCh38 chrX: 15,586,273-15,772,407 , GRCh37.p13 chrX: 15,604,396-15,790,530 PTMAP14, CA5B, 5 more genes
    nsv7085696copy number variation1nstd229human GRCh38 chrX: 15,569,980-15,802,999 , GRCh37.p13 chrX: 15,588,103-15,821,122 CLTRN, INE2, 7 more genes
    nsv7085539copy number variation1nstd229human GRCh38 chrX: 15,461,305-24,177,792 , GRCh37.p13 chrX: 15,479,428-24,195,909 LOC105373146, PIR-FIGF, 104 more genes
    nsv7085473copy number variation1nstd229human GRCh38 chrX: 15,265,887-15,855,049 , GRCh37.p13 chrX: 15,284,009-15,873,172 CLTRN, ZRSR2, 16 more genes
    nsv7085463copy number variation1nstd229human GRCh38 chrX: 15,192,575-15,841,474 , GRCh37.p13 chrX: 15,210,697-15,859,597 CA5B, AP1S2, 16 more genes
    nsv7037021inversion1nstd229human GRCh38 chrX: 14,941,162-18,599,007 , GRCh37.p13 chrX: 14,959,284-18,617,127 TXLNG, MIR4768, 54 more genes
    nsv7032726inversion1nstd229human GRCh38 chrX: 14,932,558-15,874,827 , GRCh37.p13 chrX: 14,950,680-15,892,950 INE2, HNRNPDLP5, 18 more genes
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