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Items: 1 to 20 of 264

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097655copy number variation1nstd102humanPathogenic GRCh37 chr8: 145,741,748-145,958,266 , GRCh38.p12 chr8: 144,516,364-144,732,881 RECQL4, LRRC14, 5 more genes
    nsv7072209inversion1nstd229human GRCh38 chr8: 144,433,363-144,843,412 , GRCh37.p13 chr8: 145,659,902-146,068,797 ZNF517, RN7SL395P, 26 more genes
    nsv6877856copy number variation1nstd229human GRCh38 chr8: 144,746,601-144,754,500 , GRCh37.p13 chr8: 145,971,986-145,979,885 ZNF251, LOC107986986
    nsv6876437copy number variation1nstd229human GRCh38 chr8: 144,730,697-144,734,160 , GRCh37.p13 chr8: 145,956,082-145,959,545 ZNF251, LOC107986986
    nsv6876337copy number variation1nstd229human GRCh38 chr8: 144,732,590-144,733,035 , GRCh37.p13 chr8: 145,957,975-145,958,420 ZNF251
    nsv6875883copy number variation1nstd229human GRCh38 chr8: 144,225,852-144,741,098 , GRCh37.p13 chr8: 145,280,755-145,966,483 FBXL6, MIR6848, 36 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
    nsv6873489copy number variation1nstd229human GRCh38 chr8: 144,750,804-144,757,275 , GRCh37.p13 chr8: 145,976,189-145,982,660 LOC107986986, ZNF251
    nsv6873244copy number variation1nstd229human GRCh38 chr8: 144,743,095-144,744,177 , GRCh37.p13 chr8: 145,968,480-145,969,562 LOC107986986, ZNF251
    nsv6871086copy number variation1nstd229human GRCh38 chr8: 144,722,942-144,726,068 , GRCh37.p13 chr8: 145,948,327-145,951,453 ZNF251
    nsv6866053copy number variation1nstd229human GRCh38 chr8: 144,714,266-144,720,871 , GRCh37.p13 chr8: 145,939,651-145,946,256 ZNF251, LOC100996662
    nsv6864548copy number variation1nstd229human GRCh38 chr8: 144,742,692-144,745,346 , GRCh37.p13 chr8: 145,968,077-145,970,731 LOC107986986, ZNF251
    nsv6860618copy number variation1nstd229human GRCh38 chr8: 144,695,039-144,737,011 , GRCh37.p13 chr8: 145,920,424-145,962,396 ARHGAP39, ZNF251, 2 more genes
    nsv6858944copy number variation1nstd229human GRCh38 chr8: 144,734,101-144,737,200 , GRCh37.p13 chr8: 145,959,486-145,962,585 LOC107986986, ZNF251
    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
    nsv6569976inversion1nstd223human GRCh38 chr8: 144,748,632-144,749,023 , GRCh37.p13 chr8: 145,974,017-145,974,408 LOC107986986, ZNF251
    nsv6565393inversion1nstd223human GRCh38 chr8: 144,748,369-144,749,047 , GRCh37.p13 chr8: 145,973,754-145,974,432 ZNF251, LOC107986986
    nsv6562756inversion1nstd223human GRCh38 chr8: 144,731,949-144,732,837 , GRCh37.p13 chr8: 145,957,334-145,958,222 ZNF251
    nsv6558782inversion1nstd223human GRCh38 chr8: 143,001,224-145,028,420 , GRCh37.p13 chr8: 144,082,641-146,253,806 ZFP41, LY6H, 118 more genes
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