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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923742copy number variation1nstd209human GRCh38 chr12: 21,398,810-28,763,815 , GRCh37.p13 chr12: 21,551,744-28,916,748 , LOC105369710, 101 more genes
    nsv5922804copy number variation1nstd209human GRCh38 chr12: 27,008,073-27,009,463 , GRCh37.p13 chr12: 27,161,006-27,162,396 TM7SF3
    nsv5916901copy number variation1nstd209human GRCh38 chr12: 21,398,719-28,763,765 , GRCh37.p13 chr12: 21,551,653-28,916,698 , LOC105369704, 101 more genes
    nsv5915474copy number variation1nstd209human GRCh38 chr12: 26,985,749-26,985,828 , GRCh37.p13 chr12: 27,138,682-27,138,761 TM7SF3
    nsv5912980copy number variation1nstd209human GRCh38 chr12: 25,481,034-28,003,055 , GRCh37.p13 chr12: 25,633,968-28,155,988 , ITPR2-AS1, 36 more genes
    nsv5859736copy number variation1nstd209human GRCh38 chr12: 27,007,976-27,009,475 , GRCh37.p13 chr12: 27,160,909-27,162,408 TM7SF3
    nsv5591727copy number variation1nstd207human GRCh38 chr12: 27,008,073-27,009,430 , GRCh37.p13 chr12: 27,161,006-27,162,363 TM7SF3
    nsv5507917copy number variation1nstd206human GRCh38 chr12: 26,978,143-26,979,106 , GRCh37.p13 chr12: 27,131,076-27,132,039 TM7SF3
    nsv5505177copy number variation1nstd206human GRCh38 chr12: 27,006,746-27,007,496 , GRCh37.p13 chr12: 27,159,679-27,160,429 TM7SF3
    nsv5497184copy number variation1nstd206human GRCh38 chr12: 27,008,073-27,009,464 , GRCh37.p13 chr12: 27,161,006-27,162,397 TM7SF3
    nsv5495707copy number variation1nstd206human GRCh38 chr12: 26,995,912-26,996,237 , GRCh37.p13 chr12: 27,148,845-27,149,170 TM7SF3
    nsv5355649translocation1nstd200human GRCh38 chr12: 27,008,073-27,008,073 , GRCh38 chr12: 27,009,464-27,009,464 , GRCh37.p13 chr12: 27,161,006-27,161,006 , GRCh37.p13 chr12: 27,162,397-27,162,397 TM7SF3
    nsv5343276translocation1nstd200human GRCh37 chr12: 27,162,397-27,162,397 , GRCh37 chr12: 27,161,006-27,161,006 , GRCh38.p12 chr12: 27,008,073-27,008,073 , GRCh38.p12 chr12: 27,009,464-27,009,464 TM7SF3
    nsv5265333copy number variation1nstd204human GRCh38.p13 chr12: 26,985,543-26,987,697 , GRCh37.p13 chr12: 27,138,476-27,140,630 TM7SF3
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736808copy number variation1nstd199human GRCh37 chr12: 27,160,998-27,162,360 , GRCh38.p12 chr12: 27,008,065-27,009,427 TM7SF3
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4709182copy number variation1nstd195human GRCh37 chr12: 27,057,551-27,188,451 , GRCh38.p12 chr12: 26,904,618-27,035,518 MED21, FGFR1OP2, 2 more genes
    nsv4702568copy number variation1nstd195human GRCh37 chr12: 27,057,551-27,188,401 , GRCh38.p12 chr12: 26,904,618-27,035,468 MED21, FGFR1OP2, 2 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
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