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Items: 1 to 20 of 413

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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
    nsv5691227mobile element insertion2nstd211human GRCh38 chr4: 4,422,833-4,422,833 , GRCh37.p13 chr4: 4,424,560-4,424,560 STX18
    nsv5689514mobile element insertion2nstd211human GRCh38 chr4: 4,516,026-4,516,026 , GRCh37.p13 chr4: 4,517,753-4,517,753 STX18
    nsv5684671mobile element insertion2nstd211human GRCh38 chr4: 4,532,993-4,532,993 , GRCh37.p13 chr4: 4,534,720-4,534,720 STX18
    nsv5681948mobile element insertion2nstd211human GRCh38 chr4: 4,525,308-4,525,308 , GRCh37.p13 chr4: 4,527,035-4,527,035 LOC107986254, STX18
    nsv5675578mobile element insertion1nstd211human GRCh38 chr4: 4,526,893-4,526,893 , GRCh37.p13 chr4: 4,528,620-4,528,620 STX18, LOC107986254
    nsv5673743copy number variation1nstd102humanPathogenic GRCh37 chr4: 2,200,251-5,710,240 , GRCh38.p12 chr4: 2,198,524-5,708,513 ZFYVE28, LINC01587, 81 more genes
    nsv5453796copy number variation1nstd206human GRCh38 chr4: 4,427,625-9,008,826 , GRCh37.p13 chr4: 4,429,352-9,010,552 , CPZ, 81 more genes
    nsv5409292mobile element insertion1nstd206human GRCh38 chr4: 4,422,833-4,422,884 , GRCh37.p13 chr4: 4,424,560-4,424,611 STX18
    nsv5404009mobile element insertion1nstd206human GRCh38 chr4: 4,516,026-4,516,077 , GRCh37.p13 chr4: 4,517,753-4,517,804 STX18
    nsv5399671mobile element insertion1nstd206human GRCh38 chr4: 4,532,993-4,533,044 , GRCh37.p13 chr4: 4,534,720-4,534,771 STX18
    nsv5395941mobile element insertion1nstd206human GRCh38 chr4: 4,525,308-4,525,359 , GRCh37.p13 chr4: 4,527,035-4,527,086 LOC107986254, STX18
    nsv5395382mobile element insertion1nstd206human GRCh38 chr4: 4,526,893-4,526,944 , GRCh37.p13 chr4: 4,528,620-4,528,671 LOC107986254, STX18
    nsv5367340translocation1nstd200human GRCh38 chr4: 4,585,838-4,585,838 , GRCh38 chr4: 4,510,522-4,510,522 , GRCh37.p13 chr4: 4,512,249-4,512,249 , GRCh37.p13 chr4: 4,587,565-4,587,565 STX18-AS1, STX18
    nsv5367339translocation1nstd200human GRCh38 chr4: 4,507,343-4,507,343 , GRCh38 chr4: 4,587,921-4,587,921 , GRCh37.p13 chr4: 4,509,070-4,509,070 , GRCh37.p13 chr4: 4,589,648-4,589,648 STX18, RPS7P15, 1 more genes
    nsv5192129mobile element insertion1nstd203human GRCh38 chr4: 4,450,220-4,450,235 , GRCh37.p13 chr4: 4,451,947-4,451,962 STX18
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