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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139135copy number variation1nstd232human GRCh37.p13 chr12: 133,271,507-133,271,555 , GRCh38.p12 chr12: 132,694,921-132,694,969 PXMP2
    nsv7094133copy number variation1nstd102humanUncertain significance GRCh37 chr12: 133,234,444-133,263,901 , GRCh38.p12 chr12: 132,657,858-132,687,315 POLE, PXMP2
    nsv7093960copy number variation1nstd102humanUncertain significance GRCh37 chr12: 132,414,268-133,263,901 , GRCh38.p12 chr12: 131,929,723-132,687,315 LOC107987169, NOC4L, 20 more genes
    nsv7074199inversion1nstd229human GRCh38 chr12: 123,186,434-132,825,682 , GRCh37.p13 chr12: 123,670,981-133,402,268 PIWIL1, FZD10-AS1, 187 more genes
    nsv7067298inversion1nstd229human GRCh38 chr12: 132,079,777-132,851,356 , GRCh37.p13 chr12: 132,564,322-133,427,942 LRCOL1, PGAM5, 26 more genes
    nsv6936197copy number variation1nstd229human GRCh38 chr12: 132,513,673-132,826,503 , GRCh37.p13 chr12: 133,090,259-133,403,089 RNA5SP379, ANKLE2, 11 more genes
    nsv6934654copy number variation1nstd229human GRCh38 chr12: 132,501,807-133,106,378 , GRCh37.p13 chr12: 133,078,393-133,682,964 ZNF605, LRCOL1, 23 more genes
    nsv6927841copy number variation1nstd229human GRCh38 chr12: 132,669,263-132,721,388 , GRCh37.p13 chr12: 133,245,849-133,297,974 PGAM5, POLE, 1 more genes
    nsv6927748copy number variation1nstd229human GRCh38 chr12: 132,670,201-132,697,600 , GRCh37.p13 chr12: 133,246,787-133,274,186 POLE, PXMP2
    nsv6919583copy number variation1nstd229human GRCh38 chr12: 132,675,910-132,707,051 , GRCh37.p13 chr12: 133,252,496-133,283,637 PXMP2, POLE
    nsv6919522copy number variation1nstd229human GRCh38 chr12: 132,701,156-132,710,438 , GRCh37.p13 chr12: 133,277,742-133,287,024 PXMP2, PGAM5
    nsv6637772copy number variation1nstd102humanUncertain significance GRCh37 chr12: 133,228,857-133,455,925 , GRCh38.p12 chr12: 132,652,271-132,879,339 PGAM5, ANKLE2, 8 more genes
    nsv6621425copy number variation1nstd224human GRCh37 chr12: 133,198,293-133,634,950 , GRCh38.p12 chr12: 132,621,707-133,058,364 PXMP2, P2RX2, 18 more genes
    nsv6621314copy number variation1nstd224human GRCh37 chr12: 133,112,078-133,319,864 , GRCh38.p12 chr12: 132,535,492-132,743,278 LOC100419935, P2RX2, 9 more genes
    nsv6495125copy number variation1nstd223human GRCh38 chr12: 132,694,963-132,702,121 , GRCh37.p13 chr12: 133,271,549-133,278,707 PXMP2
    nsv6495121copy number variation1nstd223human GRCh38 chr12: 132,701,429-132,702,064 , GRCh37.p13 chr12: 133,278,015-133,278,650 PXMP2
    nsv6494435copy number variation1nstd223human GRCh38 chr12: 132,692,234-132,692,334 , GRCh37.p13 chr12: 133,268,820-133,268,920 PXMP2
    nsv6494199copy number variation1nstd223human GRCh38 chr12: 132,685,401-132,688,200 , GRCh37.p13 chr12: 133,261,987-133,264,786 PXMP2, POLE
    nsv6482852copy number variation1nstd223human GRCh38 chr12: 132,694,666-132,695,027 , GRCh37.p13 chr12: 133,271,252-133,271,613 PXMP2
    nsv6481100copy number variation1nstd223human GRCh38 chr12: 132,697,660-132,698,264 , GRCh37.p13 chr12: 133,274,246-133,274,850 PXMP2
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