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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148100copy number variation1nstd102humanUncertain significance GRCh37 chr16: 21,858,865-22,361,170 , GRCh38.p12 chr16: 21,847,544-22,349,849 , GRCh38.p12 chr16|NW_017852933.1: 755,183-1,257,484 NPIPB13, EEF2K, 16 more genes
    nsv7143545copy number variation1nstd232human GRCh37.p13 chr16: 21,968,637-21,968,734 , GRCh38.p12 chr16: 21,957,316-21,957,413 , GRCh38.p12 chr16|NW_017852933.1: 1,147,625-1,147,722 UQCRC2, PDZD9
    nsv7142932insertion1nstd232human GRCh37.p13 chr16: 21,982,945-21,982,945 , GRCh38.p12 chr16: 21,971,624-21,971,624 , GRCh38.p12 chr16|NW_017852933.1: 1,133,412-1,133,412 UQCRC2, PDZD9
    nsv7137115copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,467,726-29,044,717 , GRCh38.p12 chr16: 21,456,405-29,033,396 OTOAP1, GGA2, 148 more genes
    nsv7098903copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 21,964,745-22,385,630 , GRCh38.p12 chr16: 21,953,424-22,374,309 , GRCh38.p12 chr16|NW_017852933.1: 730,730-1,151,615 CDR2, UQCRC2, 12 more genes
    nsv7093405copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 21,780,595-22,385,630 , GRCh38.p12 chr16: 21,769,274-22,374,309 , GRCh38.p12 chr16|NW_017852933.1: 730,730-1,335,506 CDR2, UQCRC2, 19 more genes
    nsv7093393copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 21,846,039-22,385,630 , GRCh38.p12 chr16: 21,834,718-22,374,309 , GRCh38.p12 chr16|NW_017852933.1: 730,730-1,270,057 CDR2, UQCRC2, 17 more genes
    nsv7076939inversion1nstd229human GRCh38 chr16: 15,569,413-22,730,334 , GRCh37.p13 chr16: 15,663,270-22,741,655 ACSM5P1, RNU6-213P, 154 more genes
    nsv7075153inversion1nstd229human GRCh38 chr16: 21,267,353-22,312,593 , GRCh37.p13 chr16: 21,278,674-22,323,914 LOC100420536, LOC646828, 32 more genes
    nsv7074804inversion1nstd229human GRCh38 chr16: 21,265,744-22,316,509 , GRCh37.p13 chr16: 21,277,065-22,327,830 SMG1P4, LOC646828, 32 more genes
    nsv7067843inversion1nstd229human GRCh38 chr16: 21,291,198-22,687,975 , GRCh37.p13 chr16: 21,302,519-22,699,296 SMG1P4, NPIPB5, 41 more genes
    nsv7066172inversion1nstd229human GRCh38 chr16: 21,576,182-22,802,537 , GRCh37.p13 chr16: 21,587,503-22,813,858 UQCRC2, VWA3A, 31 more genes
    nsv7062907inversion1nstd229human GRCh38 chr16: 21,501,792-22,437,451 , GRCh37.p13 chr16: 21,513,113-22,448,772 LOC100420536, RRN3P3, 31 more genes
    nsv7060613inversion1nstd229human GRCh38 chr16: 21,590,269-22,770,847 , GRCh37.p13 chr16: 21,601,590-22,782,168 LOC105371129, OTOAP1, 31 more genes
    nsv7058720inversion1nstd229human GRCh38 chr16: 21,529,628-23,453,946 , GRCh37.p13 chr16: 21,540,949-23,465,267 CDR2-DT, LOC105371131, 40 more genes
    nsv7058493inversion1nstd229human GRCh38 chr16: 21,334,980-22,395,842 , GRCh37.p13 chr16: 21,346,301-22,407,163 LOC101927814, METTL9, 32 more genes
    nsv6997551copy number variation1nstd229human GRCh38 chr16: 21,967,564-21,970,695 , GRCh37.p13 chr16: 21,978,885-21,982,016 PDZD9, UQCRC2
    nsv6994439copy number variation1nstd229human GRCh38 chr16: 21,988,240-21,992,709 , GRCh37.p13 chr16: 21,999,561-22,004,030 PDZD9
    nsv6992674copy number variation1nstd229human GRCh38 chr16: 22,000,601-22,013,900 , GRCh37.p13 chr16: 22,011,922-22,025,221 PDZD9, MOSMO
    nsv6990778copy number variation1nstd229human GRCh38 chr16: 21,970,476-21,973,549 , GRCh37.p13 chr16: 21,981,797-21,984,870 UQCRC2, PDZD9
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