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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5904805copy number variation1nstd209human GRCh38 chr4: 790,124-790,396 , GRCh37.p13 chr4: 783,912-784,184 CPLX1, LOC105374339
    nsv5900064copy number variation1nstd209human GRCh38 chr4: 789,911-790,064 , GRCh37.p13 chr4: 783,699-783,852 CPLX1, LOC105374339
    nsv5898808copy number variation1nstd209human GRCh38 chr4: 803,548-803,664 , GRCh37.p13 chr4: 797,336-797,452 CPLX1
    nsv5894993copy number variation1nstd209human GRCh38 chr4: 820,746-820,819 , GRCh37.p13 chr4: 814,534-814,607 CPLX1
    nsv5839489copy number variation1nstd209human GRCh38 chr4: 790,082-791,147 , GRCh37.p13 chr4: 783,870-784,935 LOC105374339, CPLX1
    nsv5673651copy number variation1nstd102humanPathogenic GRCh37 chr4: 493,125-998,181 , GRCh38.p12 chr4: 499,336-1,004,393 ATP5ME, PDE6B, 19 more genes
    nsv5623378insertion1nstd207human GRCh38 chr4: 825,979-825,979 , GRCh37.p13 chr4: 819,767-819,767 CPLX1
    nsv5577349copy number variation1nstd207human GRCh38 chr4: 789,911-790,064 , GRCh37.p13 chr4: 783,699-783,852 LOC105374339, CPLX1
    nsv5577252copy number variation1nstd207human GRCh38 chr4: 826,358-826,476 , GRCh37.p13 chr4: 820,146-820,264 CPLX1
    nsv5575755copy number variation1nstd207human GRCh38 chr4: 826,319-826,374 , GRCh37.p13 chr4: 820,107-820,162 CPLX1
    nsv5450533copy number variation1nstd206human GRCh38 chr4: 825,668-825,746 , GRCh37.p13 chr4: 819,456-819,534 CPLX1
    nsv5450324copy number variation1nstd206human GRCh38 chr4: 754,136-838,398 , GRCh37.p13 chr4: 747,924-832,186 PCGF3, LOC105374339, 2 more genes
    nsv5381775copy number variation1nstd102humanPathogenic GRCh37 chr4: 388,344-3,872,380 , GRCh38.p12 chr4: 394,555-3,870,653 RN7SL671P, HTT-AS, 96 more genes
    nsv5377600translocation1nstd200human GRCh38 chr4: 789,290-789,290 , GRCh38 chr4: 763,979-763,979 , GRCh37.p13 chr4: 757,767-757,767 , GRCh37.p13 chr4: 783,078-783,078 PCGF3, CPLX1, 1 more genes
    nsv5342321translocation1nstd200human GRCh37 chr4: 757,767-757,767 , GRCh37 chr4: 783,078-783,078 , GRCh38.p12 chr4: 763,979-763,979 , GRCh38.p12 chr4: 789,290-789,290 PCGF3, CPLX1, 1 more genes
    nsv5306437copy number variation1nstd204human GRCh38.p13 chr4: 763,976-789,292 , GRCh37.p13 chr4: 757,764-783,080 CPLX1, PCGF3, 2 more genes
    nsv5239977copy number variation1nstd204human GRCh38.p13 chr4: 789,901-790,100 , GRCh37.p13 chr4: 783,689-783,888 CPLX1, LOC105374339
    nsv5224150copy number variation1nstd204human GRCh38.p13 chr4: 826,001-826,500 , GRCh37.p13 chr4: 819,789-820,288 CPLX1
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