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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147944copy number variation1nstd232human GRCh37.p13 chr16: 8,754,665-8,754,733 , GRCh38.p12 chr16: 8,660,808-8,660,876 METTL22
    nsv7140812insertion1nstd232human GRCh37.p13 chr16: 8,739,843-8,739,843 , GRCh38.p12 chr16: 8,645,986-8,645,986 METTL22
    nsv7098957copy number variation1nstd102humanPathogenic GRCh37 chr16: 8,160,554-9,074,348 , GRCh38.p12 chr16: 8,110,552-8,980,491 ABAT, RN7SL743P, 14 more genes
    nsv7074237inversion1nstd229human GRCh38 chr16: 8,669,770-8,701,326 , GRCh37.p13 chr16: 8,763,627-8,795,183 METTL22, ABAT, 1 more genes
    nsv7072404inversion1nstd229human GRCh38 chr16: 8,651,745-8,899,782 , GRCh37.p13 chr16: 8,745,602-8,993,639 CARHSP1, USP7, 9 more genes
    nsv7063865inversion1nstd229human GRCh38 chr16: 8,212,649-8,933,109 , GRCh37.p13 chr16: 8,262,651-9,026,966 ABAT, TMEM186, 13 more genes
    nsv6976948copy number variation1nstd229human GRCh38 chr16: 8,551,898-8,622,498 , GRCh37.p13 chr16: 8,601,900-8,716,355 TMEM114, METTL22
    nsv6975922copy number variation1nstd229human GRCh38 chr16: 8,636,201-8,727,600 , GRCh37.p13 chr16: 8,730,058-8,821,457 RN7SL743P, ABAT, 2 more genes
    nsv6975808copy number variation1nstd229human GRCh38 chr16: 8,598,735-8,816,964 , GRCh37.p13 chr16: 8,692,592-8,910,821 RN7SL743P, TMEM186, 5 more genes
    nsv6974245copy number variation1nstd229human GRCh38 chr16: 8,664,101-8,710,500 , GRCh37.p13 chr16: 8,757,958-8,804,357 ABAT, METTL22, 2 more genes
    nsv6973898copy number variation1nstd229human GRCh38 chr16: 8,382,470-8,746,540 , GRCh37.p13 chr16: 8,432,472-8,840,397 LOC100131080, TMEM114, 6 more genes
    nsv6973370copy number variation1nstd229human GRCh38 chr16: 8,616,903-8,646,855 , GRCh37.p13 chr16: 8,710,760-8,740,712 METTL22
    nsv6972610copy number variation1nstd229human GRCh38 chr16: 8,626,357-8,821,538 , GRCh37.p13 chr16: 8,720,214-8,915,395 RNU7-63P, PMM2, 5 more genes
    nsv6972233copy number variation1nstd229human GRCh38 chr16: 8,600,201-8,738,100 , GRCh37.p13 chr16: 8,694,058-8,831,957 RN7SL743P, ABAT, 3 more genes
    nsv6969417copy number variation1nstd229human GRCh38 chr16: 8,665,506-9,177,685 , GRCh37.p13 chr16: 8,759,363-9,271,542 RN7SL743P, CARHSP1, 12 more genes
    nsv6969002copy number variation1nstd229human GRCh38 chr16: 8,616,178-8,711,906 , GRCh37.p13 chr16: 8,710,035-8,805,763 RNU7-63P, RN7SL743P, 2 more genes
    nsv6968672copy number variation1nstd229human GRCh38 chr16: 8,544,120-8,801,965 , GRCh37.p13 chr16: 8,594,122-8,895,822 TMEM186, PMM2, 6 more genes
    nsv6967887copy number variation1nstd229human GRCh38 chr16: 8,604,678-8,621,269 , GRCh37.p13 chr16: 8,698,535-8,715,126 METTL22
    nsv6967233copy number variation1nstd229human GRCh38 chr16: 8,631,301-8,643,996 , GRCh37.p13 chr16: 8,725,158-8,737,853 METTL22
    nsv6965370copy number variation1nstd229human GRCh38 chr16: 8,654,147-8,656,829 , GRCh37.p13 chr16: 8,748,004-8,750,686 METTL22
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