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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112661copy number variation1nstd102humanPathogenic GRCh37 chr1: 231,407,943-237,289,859 , GRCh38.p12 chr1: 231,272,197-237,126,559 LOC105373207, LOC105373210, 113 more genes
    nsv5956882insertion1nstd209human GRCh38 chr1: 235,635,572-235,635,572 , GRCh37.p13 chr1: 235,798,872-235,798,872 GNG4
    nsv5954433insertion1nstd209human GRCh38 chr1: 235,587,634-235,587,634 , GRCh37.p13 chr1: 235,750,934-235,750,934 GNG4
    nsv5875781copy number variation1nstd209human GRCh38 chr1: 235,621,938-235,627,481 , GRCh37.p13 chr1: 235,785,238-235,790,781 GNG4
    nsv5870537copy number variation1nstd209human GRCh38 chr1: 235,572,490-235,572,789 , GRCh37.p13 chr1: 235,735,790-235,736,089 GNG4
    nsv5829554copy number variation2nstd209human GRCh38 chr1: 235,625,919-235,627,527 , GRCh37.p13 chr1: 235,789,219-235,790,827 GNG4
    nsv5829553copy number variation1nstd209human GRCh38 chr1: 235,621,919-235,627,627 , GRCh37.p13 chr1: 235,785,219-235,790,927 GNG4
    nsv5714864mobile element insertion1nstd211human GRCh38 chr1: 235,546,819-235,546,819 , GRCh37.p13 chr1: 235,710,119-235,710,119 GNG4
    nsv5686567mobile element insertion1nstd211human GRCh38 chr1: 235,619,157-235,619,157 , GRCh37.p13 chr1: 235,782,457-235,782,457 GNG4
    nsv5681216mobile element insertion2nstd211human GRCh38 chr1: 235,558,563-235,558,563 , GRCh37.p13 chr1: 235,721,863-235,721,863 GNG4
    nsv5623413insertion1nstd207human GRCh38 chr1: 235,587,623-235,587,623 , GRCh37.p13 chr1: 235,750,923-235,750,923 GNG4
    nsv5614406insertion1nstd207human GRCh38 chr1: 235,635,572-235,635,572 , GRCh37.p13 chr1: 235,798,872-235,798,872 GNG4
    nsv5558330mobile element insertion1nstd206human GRCh38 chr1: 235,546,781-235,546,804 , GRCh37.p13 chr1: 235,710,081-235,710,104 GNG4
    nsv5543432insertion1nstd206human GRCh38 chr1: 235,635,572-235,635,572 , GRCh37.p13 chr1: 235,798,872-235,798,872 GNG4
    nsv5444069copy number variation1nstd206human GRCh38 chr1: 235,621,976-235,627,468 , GRCh37.p13 chr1: 235,785,276-235,790,768 GNG4
    nsv5436929copy number variation1nstd206human GRCh38 chr1: 235,556,920-235,565,264 , GRCh37.p13 chr1: 235,720,220-235,728,564 GNG4
    nsv5400138mobile element insertion1nstd206human GRCh38 chr1: 235,558,563-235,558,567 , GRCh37.p13 chr1: 235,721,863-235,721,867 GNG4
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5381130copy number variation1nstd102humanUncertain significance GRCh37 chr1: 235,613,501-235,827,941 , GRCh38.p12 chr1|NW_014040927.1: 93,778-212,205 , GRCh38.p12 chr1: 235,450,186-235,664,641 MTCYBP14, MTND3P8, 10 more genes
    nsv5363318translocation1nstd200human GRCh38 chr1: 112,903,112-112,903,112 , GRCh38 chr1: 235,617,328-235,617,328 , GRCh37.p13 chr1: 113,445,734-113,445,734 , GRCh37.p13 chr1: 235,780,628-235,780,628 GNG4
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