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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959712insertion1nstd209human GRCh38 chr9: 132,174,376-132,174,376 , GRCh37.p13 chr9: 135,049,763-135,049,763 NTNG2
    nsv5951776insertion1nstd209human GRCh38 chr9: 132,189,062-132,189,062 , GRCh37.p13 chr9: 135,064,449-135,064,449 NTNG2
    nsv5925564copy number variation1nstd209human GRCh38 chr9: 132,239,793-132,239,928 , GRCh37.p13 chr9: 135,115,180-135,115,315 NTNG2
    nsv5922264copy number variation1nstd209human GRCh38 chr9: 132,195,996-132,196,182 , GRCh37.p13 chr9: 135,071,383-135,071,569 NTNG2
    nsv5913913copy number variation1nstd209human GRCh38 chr9: 132,206,159-132,214,457 , GRCh37.p13 chr9: 135,081,546-135,089,844 NTNG2
    nsv5913519copy number variation1nstd209human GRCh38 chr9: 132,224,953-132,225,300 , GRCh37.p13 chr9: 135,100,340-135,100,687 NTNG2
    nsv5907861copy number variation1nstd209human GRCh38 chr9: 132,174,272-132,174,375 , GRCh37.p13 chr9: 135,049,659-135,049,762 NTNG2
    nsv5859920copy number variation1nstd209human GRCh38 chr9: 132,208,543-132,211,442 , GRCh37.p13 chr9: 135,083,930-135,086,829 NTNG2
    nsv5848422copy number variation1nstd209human GRCh38 chr9: 132,206,143-132,214,088 , GRCh37.p13 chr9: 135,081,530-135,089,475 NTNG2
    nsv5635887insertion1nstd207human GRCh38 chr9: 132,173,939-132,173,939 , GRCh37.p13 chr9: 135,049,326-135,049,326 NTNG2
    nsv5592511copy number variation1nstd207human GRCh38 chr9: 132,174,294-132,174,343 , GRCh37.p13 chr9: 135,049,681-135,049,730 NTNG2
    nsv5489519copy number variation1nstd206human GRCh38 chr9: 132,195,996-132,196,185 , GRCh37.p13 chr9: 135,071,383-135,071,572 NTNG2
    nsv5484166copy number variation1nstd206human GRCh38 chr9: 132,173,919-132,174,326 , GRCh37.p13 chr9: 135,049,306-135,049,713 NTNG2
    nsv5478144copy number variation1nstd206human GRCh38 chr9: 132,174,143-132,174,338 , GRCh37.p13 chr9: 135,049,530-135,049,725 NTNG2
    nsv5474789copy number variation1nstd206human GRCh38 chr9: 132,214,330-132,214,483 , GRCh37.p13 chr9: 135,089,717-135,089,870 NTNG2
    nsv5474641copy number variation1nstd206human GRCh38 chr9: 132,190,337-132,198,238 , GRCh37.p13 chr9: 135,065,724-135,073,625 NTNG2
    nsv5385881copy number variation1nstd186human GRCh37 chr9: 135,049,326-135,049,453 , GRCh38.p12 chr9: 132,173,939-132,174,066 NTNG2
    nsv5339551translocation1nstd200human GRCh37 chr9: 135,054,367-135,054,367 , GRCh37 chr9: 135,054,245-135,054,245 , GRCh38.p12 chr9: 132,178,980-132,178,980 , GRCh38.p12 chr9: 132,178,858-132,178,858 NTNG2
    nsv5333469translocation1nstd200human GRCh37 chr9: 135,100,373-135,100,373 , GRCh37 chr9: 135,100,682-135,100,682 , GRCh38.p12 chr9: 132,225,295-132,225,295 , GRCh38.p12 chr9: 132,224,986-132,224,986 NTNG2
    nsv5301524copy number variation1nstd204human GRCh38.p13 chr9: 132,195,991-132,196,189 , GRCh37.p13 chr9: 135,071,378-135,071,576 NTNG2
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