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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076836inversion1nstd229human GRCh38 chr8: 144,824,592-144,907,471 , GRCh37.p13 chr8: 146,049,977-146,132,856 ZNF7, ZNF250, 2 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
    nsv6875656copy number variation1nstd229human GRCh38 chr8: 144,844,535-144,907,912 , GRCh37.p13 chr8: 146,069,920-146,133,297 ZNF250, COMMD5, 1 more genes
    nsv6875594copy number variation1nstd229human GRCh38 chr8: 144,848,881-144,854,213 , GRCh37.p13 chr8: 146,074,266-146,079,598 COMMD5
    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
    nsv6872608copy number variation1nstd229human GRCh38 chr8: 144,845,225-144,845,265 , GRCh37.p13 chr8: 146,070,610-146,070,650 COMMD5, ZNF7
    nsv6872421copy number variation1nstd229human GRCh38 chr8: 144,850,594-144,862,011 , GRCh37.p13 chr8: 146,075,979-146,087,396 COMMD5
    nsv6872037copy number variation1nstd229human GRCh38 chr8: 144,818,638-144,843,649 , GRCh37.p13 chr8: 146,044,023-146,069,034 ZNF7, COMMD5, 1 more genes
    nsv6871695copy number variation1nstd229human GRCh38 chr8: 144,842,535-144,843,085 , GRCh37.p13 chr8: 146,067,920-146,068,470 ZNF7, COMMD5
    nsv6870398copy number variation1nstd229human GRCh38 chr8: 144,852,524-144,852,553 , GRCh37.p13 chr8: 146,077,909-146,077,938 COMMD5
    nsv6868731copy number variation1nstd229human GRCh38 chr8: 144,794,757-144,852,914 , GRCh37.p13 chr8: 146,020,142-146,078,299 COMMD5, LOC100130027, 2 more genes
    nsv6865637copy number variation1nstd229human GRCh38 chr8: 144,806,544-144,839,995 , GRCh37.p13 chr8: 146,031,929-146,065,380 COMMD5, LOC100130027, 2 more genes
    nsv6865630copy number variation1nstd229human GRCh38 chr8: 144,800,681-144,905,297 , GRCh37.p13 chr8: 146,026,066-146,130,682 ZNF250, COMMD5, 3 more genes
    nsv6864479copy number variation1nstd229human GRCh38 chr8: 144,849,773-144,849,858 , GRCh37.p13 chr8: 146,075,158-146,075,243 COMMD5
    nsv6860159copy number variation1nstd229human GRCh38 chr8: 144,847,343-144,847,674 , GRCh37.p13 chr8: 146,072,728-146,073,059 COMMD5, ZNF7
    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
    nsv6632764copy number variation1nstd224human GRCh37 chr8: 146,045,868-146,068,429 , GRCh38.p12 chr8: 144,820,483-144,843,044 ZNF7, LOC100130027, 1 more genes
    nsv6632576copy number variation1nstd224human GRCh37 chr8: 146,063,854-146,174,584 , GRCh38.p12 chr8: 144,838,469-144,949,198 ZNF16, ZNF250, 2 more genes
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