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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969981insertion1nstd209human GRCh38 chr16: 23,584,255-23,584,255 , GRCh37.p13 chr16: 23,595,576-23,595,576 NDUFAB1
    nsv5932535copy number variation1nstd209human GRCh38 chr16: 23,583,606-23,583,705 , GRCh37.p13 chr16: 23,594,927-23,595,026 NDUFAB1
    nsv5929833copy number variation1nstd209human GRCh38 chr16: 23,582,711-23,582,796 , GRCh37.p13 chr16: 23,594,032-23,594,117 NDUFAB1
    nsv5929387copy number variation1nstd209human GRCh38 chr16: 20,698,055-24,692,430 , GRCh37.p13 chr16: 20,709,377-24,703,751 , ACSM1, 87 more genes
    nsv5599112copy number variation1nstd207human GRCh38 chr16: 23,583,603-23,583,662 , GRCh37.p13 chr16: 23,594,924-23,594,983 NDUFAB1
    nsv5523642copy number variation1nstd206human GRCh38 chr16: 23,593,963-23,594,037 , GRCh37.p13 chr16: 23,605,284-23,605,358 NDUFAB1
    nsv5521755copy number variation1nstd206human GRCh38 chr16: 23,594,015-23,607,423 , GRCh37.p13 chr16: 23,605,336-23,618,744 NDUFAB1, PALB2
    nsv5390246copy number variation1nstd186human GRCh37 chr16: 23,594,927-23,595,028 , GRCh38.p12 chr16: 23,583,606-23,583,707 NDUFAB1
    nsv5368161translocation1nstd200human GRCh38 chr16: 23,596,316-23,596,316 , GRCh38 chr5: 37,387,909-37,387,909 , GRCh37.p13 chr16: 23,607,637-23,607,637 , GRCh37.p13 chr5: 37,388,011-37,388,011 WDR70, NDUFAB1
    nsv5333523translocation1nstd200human GRCh37 chr16: 23,607,637-23,607,637 , GRCh37 chr5: 37,388,011-37,388,011 , GRCh38.p12 chr16: 23,596,316-23,596,316 , GRCh38.p12 chr5: 37,387,909-37,387,909 NDUFAB1, WDR70
    nsv5325436translocation1nstd204human GRCh37.p13 chr16: 23,607,637-23,607,637 , GRCh37.p13 chr5: 37,388,011-37,388,011 , GRCh38.p13 chr16: 23,596,316-23,596,316 , GRCh38.p13 chr5: 37,387,909-37,387,909 NDUFAB1, WDR70
    nsv5311286copy number variation1nstd204human GRCh37.p13 chr16: 23,607,269-23,613,486 , GRCh38.p13 chr16: 23,595,948-23,602,165 PALB2, NDUFAB1
    nsv5272971copy number variation1nstd204human GRCh38.p13 chr16: 23,596,001-23,602,100 , GRCh37.p13 chr16: 23,607,322-23,613,421 NDUFAB1, PALB2
    nsv5265052copy number variation1nstd204human GRCh38.p13 chr16: 23,595,875-23,602,038 , GRCh37.p13 chr16: 23,607,196-23,613,359 PALB2, NDUFAB1
    nsv5264295copy number variation1nstd204human GRCh38.p13 chr16: 23,595,975-23,601,388 , GRCh37.p13 chr16: 23,607,296-23,612,709 NDUFAB1, PALB2
    nsv5200265copy number variation1nstd205human GRCh37.p13 chr16: 23,605,337-23,618,744 , GRCh38.p12 chr16: 23,594,016-23,607,423 NDUFAB1, PALB2
    nsv5184133mobile element insertion1nstd203human GRCh38 chr16: 23,584,255-23,584,255 , GRCh37.p13 chr16: 23,595,576-23,595,576 NDUFAB1
    nsv5003203copy number variation1nstd200human GRCh38 chr16: 23,595,972-23,602,136 , GRCh37.p13 chr16: 23,607,293-23,613,457 NDUFAB1, PALB2
    nsv5003202copy number variation1nstd200human GRCh38 chr16: 23,589,754-23,593,321 , GRCh37.p13 chr16: 23,601,075-23,604,642 NDUFAB1
    nsv4850743copy number variation1nstd200human GRCh37 chr16: 23,607,293-23,613,457 , GRCh38.p12 chr16: 23,595,972-23,602,136 PALB2, NDUFAB1
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