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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
    nsv7061555inversion1nstd229human GRCh38 chr12: 29,168,112-29,176,010 , GRCh37.p13 chr12: 29,321,045-29,328,943 FAR2
    nsv7060740inversion1nstd229human GRCh38 chr12: 29,223,705-29,223,739 , GRCh37.p13 chr12: 29,376,638-29,376,672 FAR2
    nsv7058136inversion1nstd229human GRCh38 chr12: 29,281,651-29,281,740 , GRCh37.p13 chr12: 29,434,584-29,434,673 LOC100506606, FAR2
    nsv6937479copy number variation1nstd229human GRCh38 chr12: 29,168,221-29,179,714 , GRCh37.p13 chr12: 29,321,154-29,332,647 FAR2
    nsv6936182copy number variation1nstd229human GRCh38 chr12: 29,207,232-29,211,149 , GRCh37.p13 chr12: 29,360,165-29,364,082 FAR2
    nsv6936132copy number variation1nstd229human GRCh38 chr12: 29,157,732-29,166,857 , GRCh37.p13 chr12: 29,310,665-29,319,790 FAR2
    nsv6934088copy number variation1nstd229human GRCh38 chr12: 29,215,676-29,215,783 , GRCh37.p13 chr12: 29,368,609-29,368,716 FAR2
    nsv6933933copy number variation1nstd229human GRCh38 chr12: 28,940,787-29,178,999 , GRCh37.p13 chr12: 29,093,720-29,331,932 FAR2, LOC101928735
    nsv6932171copy number variation1nstd229human GRCh38 chr12: 29,146,413-29,150,908 , GRCh37.p13 chr12: 29,299,346-29,303,841 FAR2
    nsv6931058copy number variation1nstd229human GRCh38 chr12: 29,315,898-29,319,261 , GRCh37.p13 chr12: 29,468,831-29,472,194 LOC100506606, FAR2
    nsv6930926copy number variation1nstd229human GRCh38 chr12: 29,198,401-29,201,200 , GRCh37.p13 chr12: 29,351,334-29,354,133 FAR2
    nsv6930867copy number variation1nstd229human GRCh38 chr12: 29,275,067-29,285,704 , GRCh37.p13 chr12: 29,428,000-29,438,637 LOC100506606, FAR2
    nsv6929121copy number variation1nstd229human GRCh38 chr12: 29,284,557-29,295,688 , GRCh37.p13 chr12: 29,437,490-29,448,621 LOC100506606, FAR2
    nsv6928870copy number variation1nstd229human GRCh38 chr12: 29,004,855-29,175,820 , GRCh37.p13 chr12: 29,157,788-29,328,753 LOC101928735, FAR2
    nsv6928676copy number variation1nstd229human GRCh38 chr12: 28,980,445-29,199,082 , GRCh37.p13 chr12: 29,133,378-29,352,015 FAR2, LOC101928735
    nsv6928564copy number variation1nstd229human GRCh38 chr12: 29,104,264-29,158,879 , GRCh37.p13 chr12: 29,257,197-29,311,812 FAR2
    nsv6926642copy number variation1nstd229human GRCh38 chr12: 29,232,300-29,237,436 , GRCh37.p13 chr12: 29,385,233-29,390,369 FAR2
    nsv6922519copy number variation1nstd229human GRCh38 chr12: 29,157,757-29,180,875 , GRCh37.p13 chr12: 29,310,690-29,333,808 FAR2
    nsv6921687copy number variation1nstd229human GRCh38 chr12: 29,276,762-29,286,241 , GRCh37.p13 chr12: 29,429,695-29,439,174 LOC100506606, FAR2
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