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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5885845copy number variation1nstd209human GRCh38 chr1: 107,354,197-107,356,728 , GRCh37.p13 chr1: 107,896,819-107,899,350 NTNG1
    nsv5882692copy number variation1nstd209human GRCh38 chr1: 107,466,079-107,466,136 , GRCh37.p13 chr1: 108,008,701-108,008,758 NTNG1
    nsv5827787copy number variation1nstd209human GRCh38 chr1: 107,360,966-107,363,256 , GRCh37.p13 chr1: 107,903,588-107,905,878 NTNG1
    nsv5827786copy number variation1nstd209human GRCh38 chr1: 107,249,836-107,255,472 , GRCh37.p13 chr1: 107,792,458-107,798,094 NTNG1
    nsv5827590copy number variation1nstd209human GRCh38 chr1: 107,354,236-107,356,765 , GRCh37.p13 chr1: 107,896,858-107,899,387 NTNG1
    nsv5827589copy number variation1nstd209human GRCh38 chr1: 107,314,369-107,315,418 , GRCh37.p13 chr1: 107,856,991-107,858,040 NTNG1
    nsv5726652mobile element insertion1nstd211human GRCh38 chr1: 107,175,814-107,175,814 , GRCh37.p13 chr1: 107,718,436-107,718,436 NTNG1
    nsv5719505mobile element insertion1nstd211human GRCh38 chr1: 107,382,278-107,382,278 , GRCh37.p13 chr1: 107,924,900-107,924,900 NTNG1
    nsv5692320mobile element insertion2nstd211human GRCh38 chr1: 107,414,264-107,414,264 , GRCh37.p13 chr1: 107,956,886-107,956,886 NTNG1
    nsv5682769mobile element insertion1nstd211human GRCh38 chr1: 107,407,236-107,407,236 , GRCh37.p13 chr1: 107,949,858-107,949,858 NTNG1
    nsv5679968mobile element insertion1nstd211human GRCh38 chr1: 107,378,109-107,378,109 , GRCh37.p13 chr1: 107,920,731-107,920,731 NTNG1
    nsv5621030insertion1nstd207human GRCh38 chr1: 107,459,282-107,459,282 , GRCh37.p13 chr1: 108,001,904-108,001,904 NTNG1
    nsv5618179insertion1nstd207human GRCh38 chr1: 107,290,968-107,290,968 , GRCh37.p13 chr1: 107,833,590-107,833,590 NTNG1
    nsv5616416insertion1nstd207human GRCh38 chr1: 107,244,776-107,244,776 , GRCh37.p13 chr1: 107,787,398-107,787,398 NTNG1
    nsv5605509insertion1nstd207human GRCh38 chr1: 107,155,157-107,155,157 , GRCh37.p13 chr1: 107,697,779-107,697,779 NTNG1
    nsv5559044sequence alteration1nstd206human GRCh38 chr1: 107,230,760-107,230,778 , GRCh37.p13 chr1: 107,773,382-107,773,400 NTNG1
    nsv5545023insertion1nstd206human GRCh38 chr1: 107,230,760-107,230,760 , GRCh37.p13 chr1: 107,773,382-107,773,382 NTNG1
    nsv5542895insertion1nstd206human GRCh38 chr1: 107,290,945-107,290,945 , GRCh37.p13 chr1: 107,833,567-107,833,567 NTNG1
    nsv5432546copy number variation1nstd206human GRCh38 chr1: 107,459,282-107,465,666 , GRCh37.p13 chr1: 108,001,904-108,008,288 NTNG1
    nsv5425762copy number variation1nstd206human GRCh38 chr1: 107,354,210-107,356,754 , GRCh37.p13 chr1: 107,896,832-107,899,376 NTNG1
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