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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6112680copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882 ADCY3, ALK, 314 more genes
    nsv5947663insertion1nstd209human GRCh38 chr2: 39,486,932-39,486,932 , GRCh37.p13 chr2: 39,714,073-39,714,073 MAP4K3-DT
    nsv5886669copy number variation1nstd209human GRCh38 chr2: 39,488,813-39,489,130 , GRCh37.p13 chr2: 39,715,954-39,716,271 MAP4K3-DT
    nsv5876011copy number variation1nstd209human GRCh38 chr2: 39,485,178-39,485,810 , GRCh37.p13 chr2: 39,712,319-39,712,951 MAP4K3-DT
    nsv5868973copy number variation1nstd209human GRCh38 chr2: 39,527,435-39,528,205 , GRCh37.p13 chr2: 39,754,576-39,755,346 MAP4K3-DT
    nsv5690931mobile element insertion2nstd211human GRCh38 chr2: 39,537,189-39,537,189 , GRCh37.p13 chr2: 39,764,330-39,764,330 MAP4K3-DT
    nsv5686139mobile element insertion1nstd211human GRCh38 chr2: 39,535,505-39,535,505 , GRCh37.p13 chr2: 39,762,646-39,762,646 MAP4K3-DT
    nsv5674617mobile element insertion2nstd211human GRCh38 chr2: 39,476,696-39,476,696 , GRCh37.p13 chr2: 39,703,837-39,703,837 MAP4K3-DT
    nsv5614076insertion1nstd207human GRCh38 chr2: 39,486,842-39,486,842 , GRCh37.p13 chr2: 39,713,983-39,713,983 MAP4K3-DT
    nsv5569535copy number variation1nstd207human GRCh38 chr2: 39,485,176-39,485,808 , GRCh37.p13 chr2: 39,712,317-39,712,949 MAP4K3-DT
    nsv5448602copy number variation1nstd206human GRCh38 chr2: 39,469,362-39,474,791 , GRCh37.p13 chr2: 39,696,503-39,701,932 MAP4K3-DT
    nsv5448175copy number variation1nstd206human GRCh38 chr2: 39,477,290-39,477,355 , GRCh37.p13 chr2: 39,704,431-39,704,496 MAP4K3-DT
    nsv5444313copy number variation1nstd206human GRCh38 chr2: 39,591,743-39,591,800 , GRCh37.p13 chr2: 39,818,883-39,818,940 MAP4K3-DT
    nsv5443820copy number variation1nstd206human GRCh38 chr2: 39,485,178-39,485,812 , GRCh37.p13 chr2: 39,712,319-39,712,953 MAP4K3-DT
    nsv5443160copy number variation1nstd206human GRCh38 chr2: 39,477,822-39,702,759 , GRCh37.p13 chr2: 39,704,963-39,929,899 MAP4K3-DT, TMEM178A
    nsv5442327copy number variation1nstd206human GRCh38 chr2: 39,527,473-39,528,175 , GRCh37.p13 chr2: 39,754,614-39,755,316 MAP4K3-DT
    nsv5440905copy number variation1nstd206human GRCh38 chr2: 39,526,569-39,528,250 , GRCh37.p13 chr2: 39,753,710-39,755,391 MAP4K3-DT
    nsv5439634copy number variation1nstd206human GRCh38 chr2: 39,574,196-39,574,463 , GRCh37.p13 chr2: 39,801,336-39,801,603 MAP4K3-DT
    nsv5437085copy number variation1nstd206human GRCh38 chr2: 39,488,891-39,491,116 , GRCh37.p13 chr2: 39,716,032-39,718,257 MAP4K3-DT
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