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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
    nsv5979532inversion1nstd209human GRCh38 chr4: 4,147,913-9,493,295 , GRCh37.p13 chr4: 4,149,640-9,494,939 , CRMP1, 130 more genes
    nsv5974394inversion1nstd209human GRCh38 chr4: 4,005,086-9,639,734 , GRCh37.p13 chr4: 4,006,813-9,641,358 , CRMP1, 142 more genes
    nsv5973087inversion1nstd209human GRCh38 chr4: 3,883,398-8,956,544 , GRCh37.p13 chr4: 3,885,125-8,958,270 , CRMP1, 102 more genes
    nsv5951554insertion1nstd209human GRCh38 chr4: 6,977,077-6,977,077 , GRCh37.p13 chr4: 6,978,804-6,978,804 TBC1D14
    nsv5889583copy number variation1nstd209human GRCh38 chr4: 7,032,406-7,032,508 , GRCh37.p13 chr4: 7,034,133-7,034,235 LOC100129931, TBC1D14
    nsv5888887copy number variation1nstd209human GRCh38 chr4: 7,025,786-7,025,931 , GRCh37.p13 chr4: 7,027,513-7,027,658 TBC1D14
    nsv5681775mobile element insertion1nstd211human GRCh38 chr4: 6,978,912-6,978,912 , GRCh37.p13 chr4: 6,980,639-6,980,639 TBC1D14
    nsv5623517insertion1nstd207human GRCh38 chr4: 6,977,689-6,977,689 , GRCh37.p13 chr4: 6,979,416-6,979,416 TBC1D14
    nsv5611967insertion1nstd207human GRCh38 chr4: 7,019,724-7,019,724 , GRCh37.p13 chr4: 7,021,451-7,021,451 TBC1D14
    nsv5610081insertion1nstd207human GRCh38 chr4: 7,019,979-7,019,979 , GRCh37.p13 chr4: 7,021,706-7,021,706 TBC1D14
    nsv5608494insertion2nstd207human GRCh38 chr4: 6,977,077-6,977,077 , GRCh37.p13 chr4: 6,978,804-6,978,804 TBC1D14
    nsv5584406copy number variation1nstd207human GRCh38 chr4: 7,019,725-7,019,886 , GRCh37.p13 chr4: 7,021,452-7,021,613 TBC1D14
    nsv5579710copy number variation1nstd207human GRCh38 chr4: 6,977,649-6,977,728 , GRCh37.p13 chr4: 6,979,376-6,979,455 TBC1D14
    nsv5579100copy number variation1nstd207human GRCh38 chr4: 6,978,007-6,978,219 , GRCh37.p13 chr4: 6,979,734-6,979,946 TBC1D14
    nsv5566114copy number variation1nstd207human GRCh38 chr4: 7,019,749-7,019,802 , GRCh37.p13 chr4: 7,021,476-7,021,529 TBC1D14
    nsv5453796copy number variation1nstd206human GRCh38 chr4: 4,427,625-9,008,826 , GRCh37.p13 chr4: 4,429,352-9,010,552 , CPZ, 81 more genes
    nsv5434776copy number variation1nstd206human GRCh38 chr4: 6,974,944-6,980,808 , GRCh37.p13 chr4: 6,976,671-6,982,535 TBC1D14
    nsv5395080mobile element insertion1nstd206human GRCh38 chr4: 6,978,912-6,978,963 , GRCh37.p13 chr4: 6,980,639-6,980,690 TBC1D14
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