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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137725copy number variation1nstd102humanUncertain significance GRCh38 chr22: 23,774,226-23,859,697 , GRCh37.p13 chr22: 24,116,413-24,201,884 SMARCB1, MMP11, 2 more genes
    nsv6123913copy number variation1nstd186human GRCh37 chr22: 24,195,941-24,198,505 , GRCh38.p12 chr22: 23,853,754-23,856,318 , GRCh38.p12 chr22|NT_187633.1: 90,116-92,680 SLC2A11
    nsv6113380mobile element insertion1nstd186human GRCh37 chr22: 24,198,551-24,198,556 , GRCh38.p12 chr22: 23,856,364-23,856,369 , GRCh38.p12 chr22|NT_187633.1: 92,726-92,731 SLC2A11
    nsv5972009insertion1nstd209human GRCh38 chr22: 23,856,318-23,856,318 , GRCh37.p13 chr22: 24,198,505-24,198,505 SLC2A11
    nsv5968000inversion1nstd209human GRCh38 chr22: 23,676,272-24,601,321 , GRCh37.p13 chr22: 24,018,459-24,997,288 , ADORA2A, 38 more genes
    nsv5958899copy number variation1nstd209human GRCh38 chr22: 22,653,852-24,634,860 , GRCh37.p13 chr22: 22,996,322-25,030,827 , LOC105372957, 122 more genes
    nsv5956621copy number variation1nstd209human GRCh38 chr22: 22,621,614-24,637,144 , GRCh37.p13 chr22: 22,964,084-25,033,111 , IGLV2-5, 125 more genes
    nsv5730910mobile element insertion2nstd211human GRCh38 chr22: 23,856,318-23,856,318 , GRCh37.p13 chr22: 24,198,505-24,198,505 SLC2A11
    nsv5703556mobile element insertion2nstd211human GRCh38 chr22: 23,856,318-23,856,318 , GRCh37.p13 chr22: 24,198,505-24,198,505 SLC2A11
    nsv5703491mobile element insertion1nstd211human GRCh38 chr22: 23,861,315-23,861,315 , GRCh37.p13 chr22: 24,203,502-24,203,502 SLC2A11
    nsv5664781insertion1nstd207human GRCh38 chr22: 23,855,202-23,855,202 , GRCh37.p13 chr22: 24,197,389-24,197,389 SLC2A11
    nsv5602115copy number variation1nstd207human GRCh38 chr22: 23,853,746-23,856,317 , GRCh37.p13 chr22: 24,195,933-24,198,504 SLC2A11
    nsv5599440copy number variation1nstd207human GRCh38 chr22: 23,881,890-23,881,956 , GRCh37.p13 chr22: 24,224,077-24,224,143 SLC2A11
    nsv5540631copy number variation1nstd206human GRCh38 chr22: 23,853,734-23,856,338 , GRCh37.p13 chr22: 24,195,921-24,198,525 SLC2A11
    nsv5535523copy number variation1nstd206human GRCh38 chr22: 23,865,046-23,865,190 , GRCh37.p13 chr22: 24,207,233-24,207,377 SLC2A11
    nsv5418824mobile element insertion1nstd206human GRCh38 chr22: 23,856,364-23,856,369 , GRCh37.p13 chr22: 24,198,551-24,198,556 SLC2A11
    nsv5393850mobile element deletion2nstd186human GRCh37 chr22: 24,195,941-24,198,505 , GRCh38.p12 chr22|NT_187633.1: 90,116-92,680 , GRCh38.p12 chr22: 23,853,754-23,856,318 SLC2A11
    nsv5381153copy number variation1nstd102humanUncertain significance GRCh37 chr22: 23,915,453-24,921,762 , GRCh38.p12 chr22: 23,573,266-24,525,794 GSTT2B, SUSD2, 37 more genes
    nsv5381087copy number variation1nstd102humanPathogenic GRCh37 chr22: 23,699,269-24,992,266 , GRCh38.p12 chr22: 23,357,082-24,596,299 LOC100129358, VPREB3, 49 more genes
    nsv5380306translocation1nstd200human GRCh38 chr19: 52,679,765-52,679,765 , GRCh38 chr22: 23,856,551-23,856,551 , GRCh37.p13 chr22: 24,198,738-24,198,738 , GRCh37.p13 chr19: 53,183,018-53,183,018 ZNF83, SLC2A11
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