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Items: 1 to 20 of 436

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5946026copy number variation1nstd209human GRCh38 chr17: 4,458,456-4,458,525 , GRCh37.p13 chr17: 4,361,751-4,361,820 SPNS3
    nsv5941777copy number variation1nstd209human GRCh38 chr17: 4,430,762-4,432,625 , GRCh37.p13 chr17: 4,334,057-4,335,920 SPNS3
    nsv5932994copy number variation1nstd209human GRCh38 chr17: 4,430,174-4,432,429 , GRCh37.p13 chr17: 4,333,469-4,335,724 SPNS3
    nsv5883602copy number variation1nstd209human GRCh38 chr17: 4,459,972-4,462,012 , GRCh37.p13 chr17: 4,363,267-4,365,307 SPNS3
    nsv5880497copy number variation1nstd209human GRCh38 chr17: 4,478,102-4,483,701 , GRCh37.p13 chr17: 4,381,397-4,386,996 SPNS3
    nsv5874802copy number variation2nstd209human GRCh38 chr17: 4,430,558-4,432,557 , GRCh37.p13 chr17: 4,333,853-4,335,852 SPNS3
    nsv5874086copy number variation1nstd209human GRCh38 chr17: 4,431,758-4,444,361 , GRCh37.p13 chr17: 4,335,053-4,347,656 SPNS3
    nsv5718751mobile element insertion1nstd211human GRCh38 chr17: 4,437,968-4,437,968 , GRCh37.p13 chr17: 4,341,263-4,341,263 SPNS3
    nsv5652778insertion1nstd207human GRCh38 chr17: 4,462,338-4,462,338 , GRCh37.p13 chr17: 4,365,633-4,365,633 SPNS3
    nsv5648980insertion1nstd207human GRCh38 chr17: 4,480,741-4,480,741 , GRCh37.p13 chr17: 4,384,036-4,384,036 SPNS3
    nsv5599616copy number variation1nstd207human GRCh38 chr17: 4,458,460-4,458,521 , GRCh37.p13 chr17: 4,361,755-4,361,816 SPNS3
    nsv5558072sequence alteration1nstd206human GRCh38 chr17: 4,304,122-4,485,497 , GRCh37.p13 chr17: 4,207,417-4,388,792 UBE2G1, SPNS3, 1 more genes
    nsv5532831copy number variation1nstd206human GRCh38 chr17: 4,437,558-4,437,643 , GRCh37.p13 chr17: 4,340,853-4,340,938 SPNS3
    nsv5529026copy number variation1nstd206human GRCh38 chr17: 4,434,598-4,437,919 , GRCh37.p13 chr17: 4,337,893-4,341,214 SPNS3
    nsv5528490copy number variation1nstd206human GRCh38 chr17: 4,432,536-4,439,220 , GRCh37.p13 chr17: 4,335,831-4,342,515 SPNS3
    nsv5527922copy number variation1nstd206human GRCh38 chr17: 4,450,656-4,451,704 , GRCh37.p13 chr17: 4,353,951-4,354,999 SPNS3
    nsv5524278copy number variation1nstd206human GRCh38 chr17: 4,479,831-4,482,866 , GRCh37.p13 chr17: 4,383,126-4,386,161 SPNS3
    nsv5520338copy number variation1nstd206human GRCh38 chr17: 4,412,815-4,481,920 , GRCh37.p13 chr17: 4,316,110-4,385,215 SPNS3
    nsv5391501copy number variation1nstd186human GRCh37 chr17: 4,361,738-4,361,792 , GRCh38.p12 chr17: 4,458,443-4,458,497 SPNS3
    nsv5358581translocation1nstd200human GRCh38 chr17: 4,437,248-4,437,248 , GRCh38 chr17: 4,436,994-4,436,994 , GRCh37.p13 chr17: 4,340,543-4,340,543 , GRCh37.p13 chr17: 4,340,289-4,340,289 SPNS3
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