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Items: 1 to 20 of 1632

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131326insertion1nstd186human GRCh37 chr21: 17,937,056-17,937,105 , GRCh38.p12 chr21: 16,564,736-16,564,785 MIR99AHG
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv6130519insertion1nstd186human GRCh37 chr21: 17,559,676-17,559,676 , GRCh38.p12 chr21: 16,187,356-16,187,356 MIR99AHG
    nsv6127105copy number variation1nstd186human GRCh37 chr21: 17,774,979-17,775,175 , GRCh38.p12 chr21: 16,402,659-16,402,855 MIR99AHG
    nsv6125661copy number variation1nstd186human GRCh37 chr21: 17,522,223-17,522,540 , GRCh38.p12 chr21: 16,149,903-16,150,220 MIR99AHG
    nsv5979325insertion1nstd209human GRCh38 chr21: 16,154,962-16,154,962 , GRCh37.p13 chr21: 17,527,282-17,527,282 MIR99AHG
    nsv5977030insertion1nstd209human GRCh38 chr21: 16,223,723-16,223,723 , GRCh37.p13 chr21: 17,596,043-17,596,043 MIR99AHG
    nsv5969132insertion1nstd209human GRCh38 chr21: 16,480,284-16,480,284 , GRCh37.p13 chr21: 17,852,604-17,852,604 MIR99AHG
    nsv5968218insertion1nstd209human GRCh38 chr21: 16,187,357-16,187,357 , GRCh37.p13 chr21: 17,559,677-17,559,677 MIR99AHG
    nsv5965857copy number variation1nstd209human GRCh38 chr21: 14,377,888-22,678,896 , GRCh37.p13 chr21: 15,750,209-24,051,216 , LOC107985508, 80 more genes
    nsv5964022copy number variation1nstd209human GRCh38 chr21: 16,398,700-16,403,032 , GRCh37.p13 chr21: 17,771,020-17,775,352 MIR99AHG
    nsv5961540copy number variation1nstd209human GRCh38 chr21: 16,332,660-16,332,748 , GRCh37.p13 chr21: 17,704,981-17,705,069 MIR99AHG
    nsv5961342copy number variation1nstd209human GRCh38 chr21: 16,532,248-16,532,340 , GRCh37.p13 chr21: 17,904,568-17,904,660 MIR99AHG
    nsv5959128copy number variation1nstd209human GRCh38 chr21: 16,404,635-16,416,854 , GRCh37.p13 chr21: 17,776,955-17,789,174 MIR99AHG
    nsv5957776copy number variation1nstd209human GRCh38 chr21: 16,290,425-16,296,222 , GRCh37.p13 chr21: 17,662,746-17,668,543 MIR99AHG
    nsv5957428copy number variation1nstd209human GRCh38 chr21: 16,571,317-16,572,281 , GRCh37.p13 chr21: 17,943,637-17,944,601 MIR99AHG
    nsv5957306copy number variation1nstd209human GRCh38 chr21: 16,593,728-16,596,318 , GRCh37.p13 chr21: 17,966,048-17,968,638 MIR99AHG
    nsv5956152copy number variation1nstd209human GRCh38 chr21: 16,149,891-16,150,219 , GRCh37.p13 chr21: 17,522,211-17,522,539 MIR99AHG
    nsv5954300copy number variation1nstd209human GRCh38 chr21: 16,503,761-16,503,986 , GRCh37.p13 chr21: 17,876,081-17,876,306 MIR99AHG
    nsv5951640copy number variation1nstd209human GRCh38 chr21: 16,402,659-16,402,854 , GRCh37.p13 chr21: 17,774,979-17,775,174 MIR99AHG
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