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Items: 1 to 20 of 229

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918291copy number variation1nstd209human GRCh38 chr11: 44,608,367-44,611,181 , GRCh37.p13 chr11: 44,629,917-44,632,731 CD82
    nsv5912175copy number variation1nstd209human GRCh38 chr11: 44,607,997-44,610,788 , GRCh37.p13 chr11: 44,629,547-44,632,338 CD82
    nsv5909463copy number variation1nstd209human GRCh38 chr11: 44,590,642-44,590,787 , GRCh37.p13 chr11: 44,612,192-44,612,337 CD82
    nsv5853345copy number variation1nstd209human GRCh38 chr11: 44,608,131-44,611,430 , GRCh37.p13 chr11: 44,629,681-44,632,980 CD82
    nsv5511765copy number variation1nstd206human GRCh38 chr11: 44,595,188-44,595,848 , GRCh37.p13 chr11: 44,616,738-44,617,398 CD82
    nsv5505612copy number variation1nstd206human GRCh38 chr11: 44,619,344-44,619,398 , GRCh37.p13 chr11: 44,640,894-44,640,948 CD82
    nsv5503555copy number variation1nstd206human GRCh38 chr11: 44,590,642-44,590,788 , GRCh37.p13 chr11: 44,612,192-44,612,338 CD82
    nsv5495038copy number variation1nstd206human GRCh38 chr11: 44,608,000-44,610,789 , GRCh37.p13 chr11: 44,629,550-44,632,339 CD82
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5355043translocation1nstd200human GRCh38 chr11: 44,595,188-44,595,188 , GRCh38 chr11: 44,595,848-44,595,848 , GRCh37.p13 chr11: 44,616,738-44,616,738 , GRCh37.p13 chr11: 44,617,398-44,617,398 CD82
    nsv5355042translocation1nstd200human GRCh38 chr11: 44,567,534-44,567,534 , GRCh38 chr11: 46,753,331-46,753,331 , GRCh37.p13 chr11: 44,589,084-44,589,084 , GRCh37.p13 chr11: 46,774,881-46,774,881 CD82, CKAP5, 1 more genes
    nsv5341021translocation1nstd200human GRCh37 chr11: 44,591,839-44,591,839 , GRCh37 chr11: 44,593,632-44,593,632 , GRCh38.p12 chr11: 44,570,289-44,570,289 , GRCh38.p12 chr11: 44,572,082-44,572,082 CD82
    nsv5338063translocation1nstd200human GRCh37 chr11: 44,617,398-44,617,398 , GRCh37 chr11: 44,616,738-44,616,738 , GRCh38.p12 chr11: 44,595,848-44,595,848 , GRCh38.p12 chr11: 44,595,188-44,595,188 CD82
    nsv5335836translocation1nstd200human GRCh37 chr11: 46,774,881-46,774,881 , GRCh37 chr11: 44,589,084-44,589,084 , GRCh38.p12 chr11: 44,567,534-44,567,534 , GRCh38.p12 chr11: 46,753,331-46,753,331 CD82, CKAP5, 1 more genes
    nsv5322374translocation1nstd204human GRCh37.p13 chr11: 44,589,084-44,589,084 , GRCh37.p13 chr11: 46,774,881-46,774,881 , GRCh38.p13 chr11: 44,567,534-44,567,534 , GRCh38.p13 chr11: 46,753,331-46,753,331 CD82, CKAP5, 1 more genes
    nsv4970897copy number variation1nstd200human GRCh38 chr11: 44,558,707-44,571,135 , GRCh37.p13 chr11: 44,580,257-44,592,685 CD82
    nsv4840137copy number variation1nstd200human GRCh37 chr11: 44,638,902-44,642,371 , GRCh38.p12 chr11: 44,617,352-44,620,821 CD82
    nsv4835051copy number variation1nstd200human GRCh37 chr11: 44,629,550-44,632,339 , GRCh38.p12 chr11: 44,608,000-44,610,789 CD82
    nsv4832536copy number variation1nstd200human GRCh37 chr11: 44,612,192-44,612,338 , GRCh38.p12 chr11: 44,590,642-44,590,788 CD82
    nsv4789392mobile element deletion1nstd200human GRCh37 chr11: 44,611,386-44,611,681 , GRCh38.p12 chr11: 44,589,836-44,590,131 CD82
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