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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7075956inversion1nstd229human GRCh38 chr12: 27,427,515-27,482,550 , GRCh37.p13 chr12: 27,580,448-27,635,483 SMCO2, BMAL2-AS1
    nsv7074185inversion1nstd229human GRCh38 chr12: 27,442,280-27,446,090 , GRCh37.p13 chr12: 27,595,213-27,599,023 BMAL2-AS1, SMCO2
    nsv7063256inversion1nstd229human GRCh38 chr12: 25,590,859-27,919,674 , GRCh37.p13 chr12: 25,743,793-28,072,607 RARS1P1, LOC101929091, 34 more genes
    nsv6937693copy number variation1nstd229human GRCh38 chr12: 27,131,001-27,643,400 , GRCh37.p13 chr12: 27,283,934-27,796,333 BMAL2, STK38L, 5 more genes
    nsv6937394copy number variation1nstd229human GRCh38 chr12: 27,477,901-27,487,900 , GRCh37.p13 chr12: 27,630,834-27,640,833 SMCO2
    nsv6935857copy number variation1nstd229human GRCh38 chr12: 27,495,210-27,502,232 , GRCh37.p13 chr12: 27,648,143-27,655,165 SMCO2, RARS1P1
    nsv6935753copy number variation1nstd229human GRCh38 chr12: 27,505,677-27,513,073 , GRCh37.p13 chr12: 27,658,610-27,666,006 SMCO2
    nsv6935087copy number variation1nstd229human GRCh38 chr12: 26,967,401-27,843,600 , GRCh37.p13 chr12: 27,120,334-27,996,533 RARS1P1, RN7SKP15, 16 more genes
    nsv6932912copy number variation1nstd229human GRCh38 chr12: 27,391,629-27,485,272 , GRCh37.p13 chr12: 27,544,562-27,638,205 BMAL2, BMAL2-AS1, 1 more genes
    nsv6932106copy number variation1nstd229human GRCh38 chr12: 27,131,201-27,643,400 , GRCh37.p13 chr12: 27,284,134-27,796,333 BMAL2, C12orf71BP, 5 more genes
    nsv6928466copy number variation1nstd229human GRCh38 chr12: 27,479,393-27,485,258 , GRCh37.p13 chr12: 27,632,326-27,638,191 SMCO2
    nsv6928344copy number variation1nstd229human GRCh38 chr12: 27,477,188-27,641,266 , GRCh37.p13 chr12: 27,630,121-27,794,199 C12orf71BP, RARS1P1, 2 more genes
    nsv6927795copy number variation1nstd229human GRCh38 chr12: 27,491,706-27,497,142 , GRCh37.p13 chr12: 27,644,639-27,650,075 SMCO2, RARS1P1
    nsv6926343copy number variation1nstd229human GRCh38 chr12: 27,243,201-28,097,100 , GRCh37.p13 chr12: 27,396,134-28,250,033 RARS1P1, PPFIBP1, 15 more genes
    nsv6925635copy number variation1nstd229human GRCh38 chr12: 27,473,439-27,473,520 , GRCh37.p13 chr12: 27,626,372-27,626,453 SMCO2
    nsv6921926copy number variation1nstd229human GRCh38 chr12: 27,452,784-27,457,818 , GRCh37.p13 chr12: 27,605,717-27,610,751 SMCO2
    nsv6621450copy number variation1nstd224human GRCh37 chr12: 27,304,878-27,799,019 , GRCh38.p12 chr12: 27,151,945-27,646,086 PPFIBP1, STK38L, 5 more genes
    nsv6593303inversion1nstd223human GRCh38 chr12: 27,463,289-27,464,626 , GRCh37.p13 chr12: 27,616,222-27,617,559 SMCO2
    nsv6589035inversion1nstd223human GRCh38 chr12: 27,490,915-27,490,969 , GRCh37.p13 chr12: 27,643,848-27,643,902 SMCO2
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