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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv5345511translocation1nstd200human GRCh37 chr22: 24,237,508-24,237,508 , GRCh37 chr22: 24,238,827-24,238,827 , GRCh38.p12 chr22: 23,896,640-23,896,640 , GRCh38.p12 chr22|NT_187633.1: 131,683-131,683 , GRCh38.p12 chr22: 23,895,321-23,895,321 , GRCh38.p12 chr22|NT_187633.1: 133,002-133,002 MIF, MIF-AS1
    nsv5327787translocation1nstd204human GRCh37.p13 chr22: 24,238,827-24,238,827 , GRCh37.p13 chr22: 24,237,508-24,237,508 , GRCh38.p13 chr22: 23,896,640-23,896,640 , GRCh38.p13 chr22: 23,895,321-23,895,321 MIF, MIF-AS1
    nsv5294062copy number variation1nstd204human GRCh38.p13 chr22: 23,854,901-24,008,900 , GRCh37.p13 chr22: 24,197,088-24,298,219 , LOC100652871, 11 more genes
    nsv5282500copy number variation1nstd204human GRCh37.p13 chr22: 24,197,088-24,274,087 , GRCh38.p13 chr22: 23,854,901-23,931,900 , MIF, 4 more genes
    nsv5035841copy number variation1nstd200human GRCh38 chr22: 23,829,374-23,917,122 , GRCh37.p13 chr22: 24,171,561-24,259,309 , MIF, 5 more genes
    nsv5033688copy number variation1nstd200human GRCh38 chr22: 23,891,511-23,894,561 , GRCh37.p13 chr22: 24,233,698-24,236,748 MIF, MIF-AS1
    nsv4869374copy number variation1nstd200human GRCh37 chr22: 24,171,561-24,259,309 , GRCh38.p12 chr22: 23,829,374-23,917,122 , GRCh38.p12 chr22|NT_187633.1: 65,736-153,484 , SLC2A11, 5 more genes
    nsv4869192copy number variation1nstd200human GRCh37 chr22: 24,233,698-24,236,748 , GRCh38.p12 chr22|NT_187633.1: 127,873-130,923 , GRCh38.p12 chr22: 23,891,511-23,894,561 MIF-AS1, MIF
    nsv4768383copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-26,483,608 , GRCh38.p12 chr22: 16,408,173-26,087,642 KRT18P62, LOC101060852, 437 more genes
    nsv4729959copy number variation1nstd102humanPathogenic GRCh37 chr22: 23,650,873-25,043,046 , GRCh38.p12 chr22: 23,308,686-24,647,079 BCRP1, SNRPD3, 55 more genes
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4729872copy number variation1nstd102humanPathogenic GRCh37 chr22: 23,258,368-25,059,827 , GRCh38.p12 chr22: 22,916,198-24,663,860 LOC105372957, RAB36, 71 more genes
    nsv4729784copy number variation1nstd102humanUncertain significance GRCh37 chr22: 23,720,181-25,066,484 , GRCh38.p12 chr22: 23,377,994-24,670,517 POM121L10P, GGTLC4P, 51 more genes
    nsv4682137copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr22: 24,129,357-24,836,024 , GRCh38.p12 chr22: 23,787,170-24,440,056 MIF, DDTL, 24 more genes
    nsv4681014copy number variation1nstd189human GRCh37.p13 chr22: 23,685,680-25,034,432 , GRCh38.p12 chr22: 23,343,493-24,638,465 , ADORA2A, 51 more genes
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