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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7053146inversion1nstd229human GRCh38 chr2: 206,253,525-206,257,442 , GRCh37.p13 chr2: 207,118,249-207,122,166 CMKLR2-AS
    nsv7042007inversion1nstd229human GRCh38 chr2: 206,253,299-206,259,706 , GRCh37.p13 chr2: 207,118,023-207,124,430 HMGN1P6, CMKLR2-AS, 1 more genes
    nsv6691411copy number variation1nstd229human GRCh38 chr2: 206,258,398-206,261,744 , GRCh37.p13 chr2: 207,123,122-207,126,468 HMGN1P6, CMKLR2-AS, 1 more genes
    nsv6685986copy number variation1nstd229human GRCh38 chr2: 206,239,905-206,243,554 , GRCh37.p13 chr2: 207,104,629-207,108,278 CMKLR2-AS
    nsv6682828copy number variation1nstd229human GRCh38 chr2: 206,235,482-206,239,789 , GRCh37.p13 chr2: 207,100,206-207,104,513 ATP5POP1, CMKLR2-AS
    nsv6681040copy number variation1nstd229human GRCh38 chr2: 206,237,933-206,255,868 , GRCh37.p13 chr2: 207,102,657-207,120,592 CMKLR2-AS
    nsv6679537copy number variation1nstd229human GRCh38 chr2: 206,212,379-206,212,463 , GRCh37.p13 chr2: 207,077,103-207,077,187 CMKLR2, CMKLR2-AS
    nsv6637127copy number variation1nstd102humanPathogenic GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658 LOC100421409, LOC100507443, 310 more genes
    nsv6551777inversion1nstd223human GRCh38 chr2: 206,253,525-206,257,443 , GRCh37.p13 chr2: 207,118,249-207,122,167 CMKLR2-AS
    nsv6550285inversion1nstd223human GRCh38 chr2: 206,245,984-206,246,349 , GRCh37.p13 chr2: 207,110,708-207,111,073 CMKLR2-AS
    nsv6548274inversion1nstd223human GRCh38 chr2: 206,248,064-206,249,136 , GRCh37.p13 chr2: 207,112,788-207,113,860 CMKLR2-AS
    nsv6351278copy number variation1nstd223human GRCh38 chr2: 206,257,442-206,259,705 , GRCh37.p13 chr2: 207,122,166-207,124,429 CMKLR2-AS, RN7SKP260, 1 more genes
    nsv6348859copy number variation1nstd223human GRCh38 chr2: 206,255,933-206,256,295 , GRCh37.p13 chr2: 207,120,657-207,121,019 CMKLR2-AS
    nsv6347766copy number variation1nstd223human GRCh38 chr2: 206,239,900-206,243,548 , GRCh37.p13 chr2: 207,104,624-207,108,272 CMKLR2-AS
    nsv6338826copy number variation1nstd223human GRCh38 chr2: 206,237,933-206,255,868 , GRCh37.p13 chr2: 207,102,657-207,120,592 CMKLR2-AS
    nsv6337305copy number variation1nstd223human GRCh38 chr2: 206,235,456-206,243,481 , GRCh37.p13 chr2: 207,100,180-207,108,205 CMKLR2-AS, ATP5POP1
    nsv6315398copy number variation1nstd102humanPathogenic GRCh37 chr2: 185,697,659-213,002,074 , GRCh38.p12 chr2: 184,832,932-212,137,349 LOC107985785, MYO1B, 381 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313730copy number variation1nstd102humanPathogenic GRCh37 chr2: 200,851,079-209,054,267 , GRCh38.p12 chr2: 199,986,356-208,189,543 RN7SKP200, PIMREGP1, 179 more genes
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