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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148264copy number variation1nstd102humanPathogenic GRCh37 chr22: 23,658,260-25,114,888 , GRCh38.p12 chr22: 23,316,073-24,718,921 LOC100421614, ZNF70, 60 more genes
    nsv7137145copy number variation1nstd102humanPathogenic GRCh37 chr22: 22,893,189-24,177,119 , GRCh38.p12 chr22: 22,550,767-23,834,932 CCDC188BP, DERL3, 99 more genes
    nsv7096341copy number variation1nstd102humanUncertain significance GRCh37 chr22: 24,108,194-24,108,482 , GRCh38.p12 chr22|NT_187633.1: 2,369-2,657 , GRCh38.p12 chr22: 23,766,007-23,766,295 CHCHD10, LOC107985577, 1 more genes
    nsv7074576inversion1nstd229human GRCh38 chr22: 22,627,224-24,221,759 , GRCh37.p13 chr22: 22,969,695-24,617,727 IGLJ1, IGLV3-25, 107 more genes
    nsv7073094inversion1nstd229human GRCh38 chr22: 22,618,607-30,089,219 , GRCh37.p13 chr22: 22,961,077-30,485,208 BCRP1, POM121L10P, 237 more genes
    nsv7072924inversion1nstd229human GRCh38 chr22: 23,614,290-25,377,289 , GRCh37.p13 chr22: 23,956,477-25,773,256 DDTL, SUSD2, 58 more genes
    nsv7071742inversion1nstd229human GRCh38 chr22: 23,575,130-25,318,153 , GRCh37.p13 chr22: 23,917,317-25,714,120 UPB1, LOC107985577, 57 more genes
    nsv7069551inversion1nstd229human GRCh38 chr22: 22,654,707-24,242,509 , GRCh37.p13 chr22: 22,997,177-24,638,477 IGLV3-27, MIF-AS1, 103 more genes
    nsv7068518inversion1nstd229human GRCh38 chr22: 22,967,696-24,261,827 , GRCh37.p13 chr22: 23,309,870-24,657,795 DDT, POM121L11P, 51 more genes
    nsv7067842inversion1nstd229human GRCh38 chr22: 23,575,725-25,317,505 , GRCh37.p13 chr22: 23,917,912-25,713,472 CHCHD10, ZNF70, 57 more genes
    nsv7063732inversion1nstd229human GRCh38 chr22: 23,598,898-25,431,054 , GRCh37.p13 chr22: 23,941,085-25,827,021 LOC100652871, CRYBB2, 58 more genes
    nsv7062268inversion1nstd229human GRCh38 chr22: 23,594,836-25,435,234 , GRCh37.p13 chr22: 23,937,023-25,831,201 KIAA1671-AS1, BCRP3, 58 more genes
    nsv7029150copy number variation1nstd229human GRCh38 chr22: 23,758,698-23,763,318 , GRCh37.p13 chr22: 24,100,885-24,105,505 C22orf15
    nsv7028873copy number variation1nstd229human GRCh38 chr22: 22,977,123-28,064,565 , GRCh37.p13 chr22: 23,319,297-28,460,553 LOC100652871, VPREB3, 132 more genes
    nsv7027713copy number variation1nstd229human GRCh38 chr22: 23,389,632-24,058,869 , GRCh37.p13 chr22: 23,731,819-24,455,332 LOC105372959, IGLL1, 32 more genes
    nsv7019205copy number variation1nstd229human GRCh38 chr22: 23,765,543-23,766,328 , GRCh37.p13 chr22: 24,107,730-24,108,515 LOC107985577, C22orf15, 1 more genes
    nsv6637831copy number variation1nstd102humanLikely pathogenic GRCh37 chr22: 23,650,201-24,992,266 , GRCh38.p12 chr22: 23,308,014-24,596,299 ADORA2A, ASLP1, 53 more genes
    nsv6637777copy number variation1nstd102humanPathogenic GRCh37 chr22: 22,997,929-24,995,256 , GRCh38.p12 chr22: 22,655,459-24,599,289 LOC105372947, GGT5, 117 more genes
    nsv6637667copy number variation1nstd102humanLikely pathogenic GRCh37 chr22: 23,650,872-25,002,483 , GRCh38.p12 chr22: 23,308,685-24,606,516 ADORA2A, ASLP1, 53 more genes
    nsv6637240copy number variation1nstd102humanLikely pathogenic GRCh37 chr22: 22,953,515-24,995,256 , GRCh38.p12 chr22: 22,611,045-24,599,289 ADORA2A, ASLP1, 122 more genes
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