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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
    nsv7076490inversion1nstd229human GRCh38 chr12: 20,940,376-25,948,754 , GRCh37.p13 chr12: 21,093,310-26,101,687 LOC102724261, IRAG2, 59 more genes
    nsv7071950inversion1nstd229human GRCh38 chr12: 25,117,703-25,121,621 , GRCh37.p13 chr12: 25,270,637-25,274,555 DNAI7
    nsv7071089inversion1nstd229human GRCh38 chr12: 24,891,778-26,817,157 , GRCh37.p13 chr12: 25,044,712-26,970,090 LOC107984475, RNA5SP354, 29 more genes
    nsv7070937inversion1nstd229human GRCh38 chr12: 25,114,365-25,121,981 , GRCh37.p13 chr12: 25,267,299-25,274,915 DNAI7
    nsv7069577inversion1nstd229human GRCh38 chr12: 24,438,408-26,775,512 , GRCh37.p13 chr12: 24,591,342-26,928,445 RN7SKP262, RNU4-67P, 35 more genes
    nsv7067422inversion1nstd229human GRCh38 chr12: 24,742,932-25,115,392 , GRCh37.p13 chr12: 24,895,866-25,268,326 DNAI7, LOC105369699, 7 more genes
    nsv6936374copy number variation1nstd229human GRCh38 chr12: 25,144,849-25,151,384 , GRCh37.p13 chr12: 25,297,783-25,304,318 DNAI7
    nsv6936283copy number variation1nstd229human GRCh38 chr12: 24,805,218-25,158,486 , GRCh37.p13 chr12: 24,958,152-25,311,420 DAD1P1, LOC105369699, 7 more genes
    nsv6935797copy number variation1nstd229human GRCh38 chr12: 24,790,701-25,149,700 , GRCh37.p13 chr12: 24,943,635-25,302,634 LINC02909, DNAI7, 7 more genes
    nsv6935781copy number variation1nstd229human GRCh38 chr12: 25,133,410-25,182,849 , GRCh37.p13 chr12: 25,286,344-25,335,783 DNAI7
    nsv6930394copy number variation1nstd229human GRCh38 chr12: 25,147,430-25,153,176 , GRCh37.p13 chr12: 25,300,364-25,306,110 DNAI7
    nsv6930044copy number variation1nstd229human GRCh38 chr12: 24,537,362-25,205,348 , GRCh37.p13 chr12: 24,690,296-25,358,282 SOX5, LINC02909, 15 more genes
    nsv6927393copy number variation1nstd229human GRCh38 chr12: 25,108,063-25,108,190 , GRCh37.p13 chr12: 25,260,997-25,261,124 DNAI7, IRAG2
    nsv6925539copy number variation1nstd229human GRCh38 chr12: 24,922,823-25,184,949 , GRCh37.p13 chr12: 25,075,757-25,337,883 BCAT1, LINC02909, 5 more genes
    nsv6924791copy number variation1nstd229human GRCh38 chr12: 25,111,005-25,114,995 , GRCh37.p13 chr12: 25,263,939-25,267,929 DNAI7
    nsv6922111copy number variation1nstd229human GRCh38 chr12: 24,709,960-25,120,876 , GRCh37.p13 chr12: 24,862,894-25,273,810 IRAG2, LOC105369699, 7 more genes
    nsv6922060copy number variation1nstd229human GRCh38 chr12: 25,132,487-25,132,944 , GRCh37.p13 chr12: 25,285,421-25,285,878 DNAI7
    nsv6921964copy number variation1nstd229human GRCh38 chr12: 25,147,277-25,151,515 , GRCh37.p13 chr12: 25,300,211-25,304,449 DNAI7
    nsv6919851copy number variation1nstd229human GRCh38 chr12: 24,734,688-25,110,977 , GRCh37.p13 chr12: 24,887,622-25,263,911 CENPUP2, LOC105369699, 7 more genes
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