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Items: 1 to 20 of 293

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5913433copy number variation1nstd209human GRCh38 chr10: 120,898,928-120,898,988 , GRCh37.p13 chr10: 122,658,440-122,658,500 WDR11
    nsv5861340copy number variation1nstd209human GRCh38 chr10: 120,848,381-120,850,145 , GRCh37.p13 chr10: 122,607,893-122,609,657 WDR11-DT, WDR11
    nsv5725073mobile element insertion2nstd211human GRCh38 chr10: 120,902,679-120,902,679 , GRCh37.p13 chr10: 122,662,191-122,662,191 WDR11, LOC105378519
    nsv5721715mobile element insertion1nstd211human GRCh38 chr10: 120,892,711-120,892,711 , GRCh37.p13 chr10: 122,652,223-122,652,223 WDR11
    nsv5711316mobile element insertion1nstd211human GRCh38 chr10: 120,872,628-120,872,628 , GRCh37.p13 chr10: 122,632,140-122,632,140 WDR11
    nsv5672603copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 119,302,758-124,813,305 , GRCh38.p12 chr10: 117,543,247-123,053,789 ACADSB, DMBT1, 84 more genes
    nsv5628171insertion1nstd207human GRCh38 chr10: 120,902,665-120,902,665 , GRCh37.p13 chr10: 122,662,177-122,662,177 WDR11, LOC105378519
    nsv5555829sequence alteration1nstd206human GRCh38 chr10: 120,861,989-120,864,166 , GRCh37.p13 chr10: 122,621,501-122,623,678 WDR11
    nsv5555773mobile element insertion1nstd206human GRCh38 chr10: 120,892,711-120,892,762 , GRCh37.p13 chr10: 122,652,223-122,652,274 WDR11
    nsv5554904mobile element insertion1nstd206human GRCh38 chr10: 120,902,679-120,902,730 , GRCh37.p13 chr10: 122,662,191-122,662,242 LOC105378519, WDR11
    nsv5541000insertion1nstd206human GRCh38 chr10: 120,864,157-120,864,157 , GRCh37.p13 chr10: 122,623,669-122,623,669 WDR11
    nsv5508501copy number variation1nstd206human GRCh38 chr10: 120,728,000-121,028,734 , GRCh37.p13 chr10: 122,487,512-122,788,247 , WDR11, 5 more genes
    nsv5504034copy number variation1nstd206human GRCh38 chr10: 120,852,992-120,853,125 , GRCh37.p13 chr10: 122,612,504-122,612,637 WDR11
    nsv5401077mobile element insertion1nstd206human GRCh38 chr10: 120,872,628-120,872,679 , GRCh37.p13 chr10: 122,632,140-122,632,191 WDR11
    nsv5373307translocation1nstd200human GRCh38 chr10: 120,877,680-120,877,680 , GRCh38 chr10: 120,875,881-120,875,881 , GRCh37.p13 chr10: 122,635,393-122,635,393 , GRCh37.p13 chr10: 122,637,192-122,637,192 WDR11
    nsv5373306translocation1nstd200human GRCh38 chr10: 120,864,157-120,864,157 , GRCh38 chr10: 120,862,291-120,862,291 , GRCh37.p13 chr10: 122,621,803-122,621,803 , GRCh37.p13 chr10: 122,623,669-122,623,669 WDR11
    nsv5373305translocation1nstd200human GRCh38 chr10: 120,861,990-120,861,990 , GRCh38 chr10: 120,864,167-120,864,167 , GRCh37.p13 chr10: 122,623,679-122,623,679 , GRCh37.p13 chr10: 122,621,502-122,621,502 WDR11
    nsv5333232translocation1nstd200human GRCh37 chr10: 122,623,679-122,623,679 , GRCh37 chr10: 122,621,503-122,621,503 , GRCh38.p12 chr10: 120,864,167-120,864,167 , GRCh38.p12 chr10: 120,861,991-120,861,991 WDR11
    nsv5303429copy number variation1nstd204human GRCh38.p13 chr10: 120,875,866-120,877,689 , GRCh37.p13 chr10: 122,635,378-122,637,201 WDR11
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