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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129069copy number variation1nstd186human GRCh37 chr17: 4,640,607-4,641,461 , GRCh38.p12 chr17: 4,737,312-4,738,166 ZMYND15, CXCL16
    nsv5938892copy number variation1nstd209human GRCh38 chr17: 4,737,398-4,737,930 , GRCh37.p13 chr17: 4,640,693-4,641,225 CXCL16, ZMYND15
    nsv5928622copy number variation1nstd209human GRCh38 chr17: 4,737,312-4,738,039 , GRCh37.p13 chr17: 4,640,607-4,641,334 ZMYND15, CXCL16
    nsv5880945copy number variation1nstd209human GRCh38 chr17: 4,735,876-4,737,075 , GRCh37.p13 chr17: 4,639,171-4,640,370 CXCL16
    nsv5585319copy number variation1nstd207human GRCh38 chr17: 4,737,312-4,738,039 , GRCh37.p13 chr17: 4,640,607-4,641,334 CXCL16, ZMYND15
    nsv5514507copy number variation1nstd206human GRCh38 chr17: 4,737,312-4,738,166 , GRCh37.p13 chr17: 4,640,607-4,641,461 CXCL16, ZMYND15
    nsv5391685copy number variation2nstd186human GRCh37 chr17: 4,640,607-4,641,336 , GRCh38.p12 chr17: 4,737,312-4,738,041 ZMYND15, CXCL16
    nsv5389605copy number variation1nstd186human GRCh37 chr17: 4,640,740-4,641,210 , GRCh38.p12 chr17: 4,737,445-4,737,915 ZMYND15, CXCL16
    nsv5382380mobile element deletion1nstd186human GRCh37 chr17: 4,640,590-4,640,894 , GRCh38.p12 chr17: 4,737,295-4,737,599 CXCL16
    nsv5325509translocation1nstd204human GRCh37.p13 chr17: 4,641,221-4,641,221 , GRCh37.p13 chr17: 4,640,741-4,640,741 , GRCh38.p13 chr17: 4,737,926-4,737,926 , GRCh38.p13 chr17: 4,737,446-4,737,446 CXCL16, ZMYND15
    nsv5323959translocation1nstd204human GRCh37.p13 chr17: 4,640,607-4,640,607 , GRCh37.p13 chr17: 4,641,336-4,641,336 , GRCh38.p13 chr17: 4,737,312-4,737,312 , GRCh38.p13 chr17: 4,738,041-4,738,041 CXCL16, ZMYND15
    nsv5299082copy number variation1nstd204human GRCh37.p13 chr17: 4,627,696-4,727,995 , GRCh38.p13 chr17: 4,724,401-4,824,700 PLD2, PSMB6, 6 more genes
    nsv5015593copy number variation1nstd200human GRCh38 chr17: 4,737,312-4,738,041 , GRCh37.p13 chr17: 4,640,607-4,641,336 CXCL16, ZMYND15
    nsv4907306mobile element deletion1nstd200human GRCh38 chr17: 4,737,260-4,737,602 , GRCh37.p13 chr17: 4,640,555-4,640,897 CXCL16
    nsv4857825copy number variation1nstd200human GRCh37 chr17: 4,640,738-4,641,211 , GRCh38.p12 chr17: 4,737,443-4,737,916 CXCL16, ZMYND15
    nsv4857824copy number variation1nstd200human GRCh37 chr17: 4,640,607-4,641,336 , GRCh38.p12 chr17: 4,737,312-4,738,041 CXCL16, ZMYND15
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4744878copy number variation1nstd199human GRCh37 chr17: 4,640,713-4,641,264 , GRCh38.p12 chr17: 4,737,418-4,737,969 CXCL16, ZMYND15
    nsv4674912copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088 SRR, DBIL5P, 196 more genes
    nsv4670077copy number variation1nstd186human GRCh37 chr17: 4,643,297-4,643,341 , GRCh38.p12 chr17: 4,740,002-4,740,046 ZMYND15, CXCL16
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