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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969964insertion1nstd209human GRCh38 chr12: 51,834,018-51,834,018 , GRCh37.p13 chr12: 52,227,802-52,227,802 FIGNL2
    nsv5930187copy number variation1nstd209human GRCh38 chr12: 51,834,012-51,834,099 , GRCh37.p13 chr12: 52,227,796-52,227,883 FIGNL2
    nsv5853105copy number variation1nstd209human GRCh38 chr12: 51,846,410-51,848,000 , GRCh37.p13 chr12: 52,240,194-52,241,784 FIGNL2, FIGNL2-DT
    nsv5650201insertion1nstd207human GRCh38 chr12: 51,834,082-51,834,082 , GRCh37.p13 chr12: 52,227,866-52,227,866 FIGNL2
    nsv5647803insertion1nstd207human GRCh38 chr12: 51,834,018-51,834,018 , GRCh37.p13 chr12: 52,227,802-52,227,802 FIGNL2
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv4985595copy number variation1nstd200human GRCh38 chr12: 51,836,498-51,898,227 , GRCh37.p13 chr12: 52,230,282-52,292,011 LOC102724178, ANKRD33, 2 more genes
    nsv4972687copy number variation1nstd200human GRCh38 chr12: 51,829,991-51,830,672 , GRCh37.p13 chr12: 52,223,775-52,224,456 FIGNL2
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4754665insertion1nstd199human GRCh37 chr12: 52,227,800-52,227,800 , GRCh38.p12 chr12: 51,834,016-51,834,016 FIGNL2
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4671359copy number variation1nstd186human GRCh37 chr12: 52,211,801-52,215,800 , GRCh38.p12 chr12: 51,818,017-51,822,016 FIGNL2
    nsv4606453copy number variation1nstd183human GRCh37 chr12: 52,214,341-52,215,854 , GRCh38.p12 chr12: 51,820,557-51,822,070 FIGNL2
    nsv4605163copy number variation1nstd183human GRCh37 chr12: 52,211,801-52,215,800 , GRCh38.p12 chr12: 51,818,017-51,822,016 FIGNL2
    nsv4559196inversion1nstd166human GRCh37.p13 chr12: 51,569,865-55,219,228 , GRCh38.p12 chr12: 51,176,082-54,825,444 , EIF4B, 163 more genes
    nsv4438033insertion1nstd175human GRCh37 chr12: 52,227,866-52,227,866 , GRCh38.p12 chr12: 51,834,082-51,834,082 FIGNL2
    nsv4429665copy number variation1nstd174human GRCh37 chr12: 52,213,258-52,217,095 , GRCh38.p12 chr12: 51,819,474-51,823,311 FIGNL2
    nsv4425671copy number variation1nstd174human GRCh37 chr12: 52,211,645-52,215,992 , GRCh38.p12 chr12: 51,817,861-51,822,208 FIGNL2
    nsv4424089copy number variation1nstd174human GRCh37 chr12: 52,214,321-52,215,864 , GRCh38.p12 chr12: 51,820,537-51,822,080 FIGNL2
    nsv4421873copy number variation1nstd174human GRCh37 chr12: 52,201,114-52,291,700 , GRCh38.p12 chr12: 51,807,330-51,897,916 SCN8A, ANKRD33, 3 more genes
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