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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6935902copy number variation1nstd229human GRCh38 chr12: 120,319,320-120,323,629 , GRCh37.p13 chr12: 120,757,123-120,761,432 PLA2G1B
    nsv6935163copy number variation1nstd229human GRCh38 chr12: 120,067,201-120,694,800 , GRCh37.p13 chr12: 120,505,005-121,132,603 RPL11P5, RNF10, 30 more genes
    nsv6934866copy number variation1nstd229human GRCh38 chr12: 119,918,701-123,974,100 , GRCh37.p13 chr12: 120,356,505-124,458,647 RNU6-1088P, LOC105370042, 130 more genes
    nsv6932504copy number variation1nstd229human GRCh38 chr12: 120,318,511-120,325,229 , GRCh37.p13 chr12: 120,756,314-120,763,032 PLA2G1B
    nsv6931128copy number variation1nstd229human GRCh38 chr12: 120,324,906-120,328,397 , GRCh37.p13 chr12: 120,762,709-120,766,200 PLA2G1B
    nsv6930227copy number variation1nstd229human GRCh38 chr12: 120,250,901-120,560,500 , GRCh37.p13 chr12: 120,688,704-120,998,303 RNU6-1088P, RNF10, 17 more genes
    nsv6930083copy number variation1nstd229human GRCh38 chr12: 120,251,001-120,606,400 , GRCh37.p13 chr12: 120,688,804-121,044,203 COX6A1, NRAV, 19 more genes
    nsv6923885copy number variation1nstd229human GRCh38 chr12: 120,317,707-120,329,824 , GRCh37.p13 chr12: 120,755,510-120,767,627 PLA2G1B
    nsv6922382copy number variation1nstd229human GRCh38 chr12: 120,324,726-120,336,680 , GRCh37.p13 chr12: 120,762,529-120,774,483 PLA2G1B
    nsv6919599copy number variation1nstd229human GRCh38 chr12: 119,989,801-120,740,500 , GRCh37.p13 chr12: 120,427,605-121,178,303 RPS20P31, MLEC, 33 more genes
    nsv6637895copy number variation1nstd102humanUncertain significance GRCh37 chr12: 120,665,945-120,951,612 , GRCh38.p12 chr12: 120,228,142-120,513,809 SIRT4, RPS20P31, 16 more genes
    nsv6637490copy number variation1nstd102humanUncertain significance GRCh37 chr12: 120,761,046-121,280,839 , GRCh38.p12 chr12: 120,323,243-120,843,036 RPS27P25, MIR4700, 22 more genes
    nsv6583876inversion1nstd223human GRCh38 chr12: 118,054,469-123,705,974 , GRCh37.p13 chr12: 118,492,274-124,190,521 RPL11P5, RPL17P37, 159 more genes
    nsv6290239copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809 ACADS, BCL7A, 356 more genes
    nsv6132411copy number variation1nstd213human GRCh37 chr12: 119,880,000-120,880,001 , GRCh38.p12 chr12: 119,442,195-120,442,198 MSI1, RPLP0, 25 more genes
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5319747copy number variation1nstd204human GRCh38.p13 chr12: 120,322,739-120,322,877 , GRCh37.p13 chr12: 120,760,542-120,760,680 PLA2G1B
    nsv4995971copy number variation1nstd200human GRCh38 chr12: 120,320,722-120,323,282 , GRCh37.p13 chr12: 120,758,525-120,761,085 PLA2G1B
    nsv4995970copy number variation1nstd200human GRCh38 chr12: 120,317,706-120,329,823 , GRCh37.p13 chr12: 120,755,509-120,767,626 PLA2G1B
    nsv4993755copy number variation1nstd200human GRCh38 chr12: 120,309,362-120,320,787 , GRCh37.p13 chr12: 120,747,165-120,758,590 SIRT4, RNU6-1088P, 1 more genes
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