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Items: 1 to 20 of 551

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926354copy number variation1nstd209human GRCh38 chr9: 137,102,660-137,103,171 , GRCh37.p13 chr9: 139,997,112-139,997,623 MAN1B1
    nsv5923771copy number variation1nstd209human GRCh38 chr9: 137,104,728-137,104,861 , GRCh37.p13 chr9: 139,999,180-139,999,313 MAN1B1
    nsv5643481insertion1nstd207human GRCh38 chr9: 137,102,243-137,102,243 , GRCh37.p13 chr9: 139,996,695-139,996,695 MAN1B1
    nsv5642083insertion1nstd207human GRCh38 chr9: 137,102,011-137,102,011 , GRCh37.p13 chr9: 139,996,463-139,996,463 MAN1B1
    nsv5630070insertion3nstd207human GRCh38 chr9: 137,102,262-137,102,262 , GRCh37.p13 chr9: 139,996,714-139,996,714 MAN1B1
    nsv5627488insertion1nstd207human GRCh38 chr9: 137,102,825-137,102,825 , GRCh37.p13 chr9: 139,997,277-139,997,277 MAN1B1
    nsv5534707insertion1nstd206human GRCh38 chr9: 137,104,867-137,104,867 , GRCh37.p13 chr9: 139,999,319-139,999,319 MAN1B1
    nsv5492946copy number variation1nstd206human GRCh38 chr9: 137,092,135-137,093,102 , GRCh37.p13 chr9: 139,986,587-139,987,554 MAN1B1
    nsv5479244copy number variation1nstd206human GRCh38 chr9: 137,102,321-137,102,722 , GRCh37.p13 chr9: 139,996,773-139,997,174 MAN1B1
    nsv5476786copy number variation1nstd206human GRCh38 chr9: 137,089,520-137,089,635 , GRCh37.p13 chr9: 139,983,972-139,984,087 MAN1B1
    nsv5475406copy number variation1nstd206human GRCh38 chr9: 137,105,077-137,105,290 , GRCh37.p13 chr9: 139,999,529-139,999,742 MAN1B1
    nsv5381762copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,284,464-141,018,984 , GRCh38.p12 chr9: 136,390,012-138,124,532 ARRDC1, SETP5, 101 more genes
    nsv5381736copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,764,148-141,066,491 , GRCh38.p12 chr9: 136,869,696-138,172,039 PTGDS, LCN12, 63 more genes
    nsv5381735copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,984,917-139,991,370 , GRCh38 chr9: 137,090,465-137,096,918 MAN1B1
    nsv5379568translocation1nstd200human GRCh38 chr9: 137,103,766-137,103,766 , GRCh38 chr9: 137,102,437-137,102,437 , GRCh37.p13 chr9: 139,996,889-139,996,889 , GRCh37.p13 chr9: 139,998,218-139,998,218 MAN1B1
    nsv5315013copy number variation1nstd204human GRCh38.p13 chr9: 137,101,653-137,122,925 , GRCh37.p13 chr9: 139,996,105-140,017,377 DPP7, MAN1B1
    nsv5314554copy number variation1nstd204human GRCh38.p13 chr9: 137,101,628-137,104,318 , GRCh37.p13 chr9: 139,996,080-139,998,770 MAN1B1
    nsv5258661copy number variation1nstd204human GRCh38.p13 chr9: 137,101,801-137,104,000 , GRCh37.p13 chr9: 139,996,253-139,998,452 MAN1B1
    nsv5257399copy number variation1nstd204human GRCh38.p13 chr9: 137,087,836-137,088,935 , GRCh37.p13 chr9: 139,982,288-139,983,387 MAN1B1
    nsv5257294copy number variation1nstd204human GRCh38.p13 chr9: 137,091,336-137,094,453 , GRCh37.p13 chr9: 139,985,788-139,988,905 MAN1B1
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