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Items: 1 to 20 of 493

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6120995copy number variation1nstd186human GRCh37 chr9: 131,412,068-131,413,976 , GRCh38.p12 chr9: 128,649,789-128,651,697 DYNC2I2, VTI1BP4
    nsv5959614insertion1nstd209human GRCh38 chr9: 128,655,335-128,655,335 , GRCh37.p13 chr9: 131,417,614-131,417,614 DYNC2I2
    nsv5926273copy number variation1nstd209human GRCh38 chr9: 128,649,777-128,651,696 , GRCh37.p13 chr9: 131,412,056-131,413,975 VTI1BP4, DYNC2I2
    nsv5919922copy number variation1nstd209human GRCh38 chr9: 128,643,022-128,643,144 , GRCh37.p13 chr9: 131,405,301-131,405,423 DYNC2I2
    nsv5915833copy number variation1nstd209human GRCh38 chr9: 128,656,391-128,656,452 , GRCh37.p13 chr9: 131,418,670-131,418,731 DYNC2I2
    nsv5911208copy number variation1nstd209human GRCh38 chr9: 128,637,697-128,640,263 , GRCh37.p13 chr9: 131,399,976-131,402,542 DYNC2I2
    nsv5909836copy number variation1nstd209human GRCh38 chr9: 128,649,753-128,653,718 , GRCh37.p13 chr9: 131,412,032-131,415,997 VTI1BP4, DYNC2I2
    nsv5862674copy number variation1nstd209human GRCh38 chr9: 128,637,693-128,640,292 , GRCh37.p13 chr9: 131,399,972-131,402,571 DYNC2I2
    nsv5856223copy number variation1nstd209human GRCh38 chr9: 128,649,969-128,651,703 , GRCh37.p13 chr9: 131,412,248-131,413,982 DYNC2I2, VTI1BP4
    nsv5854256copy number variation1nstd209human GRCh38 chr9: 128,647,138-128,648,337 , GRCh37.p13 chr9: 131,409,417-131,410,616 DYNC2I2
    nsv5848537copy number variation1nstd209human GRCh38 chr9: 128,651,604-128,653,803 , GRCh37.p13 chr9: 131,413,883-131,416,082 VTI1BP4, DYNC2I2
    nsv5673819copy number variation1nstd102humanLikely benign GRCh37 chr9: 131,386,597-131,399,316 , GRCh38.p12 chr9: 128,624,318-128,637,037 SPTAN1, DYNC2I2
    nsv5601898copy number variation1nstd207human GRCh38 chr9: 128,649,777-128,651,696 , GRCh37.p13 chr9: 131,412,056-131,413,975 DYNC2I2, VTI1BP4
    nsv5596709copy number variation1nstd207human GRCh38 chr9: 128,649,709-128,653,708 , GRCh37.p13 chr9: 131,411,988-131,415,987 VTI1BP4, DYNC2I2
    nsv5490585copy number variation1nstd206human GRCh38 chr9: 128,643,022-128,643,148 , GRCh37.p13 chr9: 131,405,301-131,405,427 DYNC2I2
    nsv5489197copy number variation1nstd206human GRCh38 chr9: 128,649,789-128,651,697 , GRCh37.p13 chr9: 131,412,068-131,413,976 VTI1BP4, DYNC2I2
    nsv5474848copy number variation1nstd206human GRCh38 chr9: 128,649,709-128,653,778 , GRCh37.p13 chr9: 131,411,988-131,416,057 DYNC2I2, VTI1BP4
    nsv5386717copy number variation1nstd186human GRCh37 chr9: 131,412,131-131,413,703 , GRCh38.p12 chr9: 128,649,852-128,651,424 DYNC2I2, VTI1BP4
    nsv5385501copy number variation1nstd186human GRCh37 chr9: 131,412,121-131,413,919 , GRCh38.p12 chr9: 128,649,842-128,651,640 DYNC2I2, VTI1BP4
    nsv5305401copy number variation1nstd204human GRCh38.p13 chr9: 128,642,099-128,642,512 , GRCh37.p13 chr9: 131,404,378-131,404,791 DYNC2I2
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