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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146718insertion1nstd232human GRCh37.p13 chr12: 52,227,809-52,227,809 , GRCh38.p12 chr12: 51,834,025-51,834,025 FIGNL2
    nsv7140208insertion1nstd232human GRCh37.p13 chr12: 52,227,802-52,227,802 , GRCh38.p12 chr12: 51,834,018-51,834,018 FIGNL2
    nsv7138794insertion1nstd232human GRCh37.p13 chr12: 52,227,866-52,227,866 , GRCh38.p12 chr12: 51,834,082-51,834,082 FIGNL2
    nsv7076214inversion1nstd229human GRCh38 chr12: 51,539,185-51,909,086 , GRCh37.p13 chr12: 51,932,969-52,302,870 FIGNL2, HNRNPA3P10, 5 more genes
    nsv7069901inversion1nstd229human GRCh38 chr12: 51,176,082-54,825,440 , GRCh37.p13 chr12: 51,569,865-55,219,224 , HOXC5, 158 more genes
    nsv7064315inversion1nstd229human GRCh38 chr12: 51,846,741-51,846,877 , GRCh37.p13 chr12: 52,240,525-52,240,661 FIGNL2-DT, FIGNL2
    nsv6937165copy number variation1nstd229human GRCh38 chr12: 51,830,401-51,834,200 , GRCh37.p13 chr12: 52,224,185-52,227,984 FIGNL2
    nsv6931969copy number variation1nstd229human GRCh38 chr12: 51,836,498-51,898,227 , GRCh37.p13 chr12: 52,230,282-52,292,011 FIGNL2-DT, LOC102724178, 2 more genes
    nsv6928157copy number variation1nstd229human GRCh38 chr12: 51,820,539-51,821,033 , GRCh37.p13 chr12: 52,214,323-52,214,817 FIGNL2
    nsv6922244copy number variation1nstd229human GRCh38 chr12: 51,827,653-51,829,321 , GRCh37.p13 chr12: 52,221,437-52,223,105 FIGNL2
    nsv6579705inversion1nstd223human GRCh38 chr12: 51,830,154-51,830,742 , GRCh37.p13 chr12: 52,223,938-52,224,526 FIGNL2
    nsv6466568copy number variation1nstd223human GRCh38 chr12: 51,836,498-51,898,227 , GRCh37.p13 chr12: 52,230,282-52,292,011 ANKRD33, FIGNL2-DT, 2 more genes
    nsv6289529insertion1nstd214human GRCh38 chr12: 51,833,950-51,833,950 , GRCh37.p13 chr12: 52,227,734-52,227,734 FIGNL2
    nsv6288793insertion1nstd214human GRCh38 chr12: 51,834,015-51,834,015 , GRCh37.p13 chr12: 52,227,799-52,227,799 FIGNL2
    nsv6288597insertion1nstd214human GRCh38 chr12: 51,834,101-51,834,101 , GRCh37.p13 chr12: 52,227,885-52,227,885 FIGNL2
    nsv6286929insertion4nstd214human GRCh38 chr12: 51,834,082-51,834,082 , GRCh37.p13 chr12: 52,227,866-52,227,866 FIGNL2
    nsv6286369insertion2nstd214human GRCh38 chr12: 51,834,025-51,834,025 , GRCh37.p13 chr12: 52,227,809-52,227,809 FIGNL2
    nsv6286368insertion1nstd214human GRCh38 chr12: 51,834,021-51,834,021 , GRCh37.p13 chr12: 52,227,805-52,227,805 FIGNL2
    nsv6285799insertion1nstd214human GRCh38 chr12: 51,834,032-51,834,032 , GRCh37.p13 chr12: 52,227,816-52,227,816 FIGNL2
    nsv6285355insertion1nstd214human GRCh38 chr12: 51,834,012-51,834,012 , GRCh37.p13 chr12: 52,227,796-52,227,796 FIGNL2
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