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Items: 1 to 20 of 1608

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976419inversion1nstd209human GRCh38 chr7: 67,210,788-72,603,267 , GRCh37.p13 chr7: 66,675,775-71,935,721 , PMS2P4, 38 more genes
    nsv5962891insertion1nstd209human GRCh38 chr7: 71,265,119-71,265,119 , GRCh37.p13 chr7: 70,730,105-70,730,105 GALNT17
    nsv5959522insertion1nstd209human GRCh38 chr7: 71,184,966-71,184,966 , GRCh37.p13 chr7: 70,649,952-70,649,952 GALNT17
    nsv5957429insertion1nstd209human GRCh38 chr7: 71,245,848-71,245,848 , GRCh37.p13 chr7: 70,710,834-70,710,834 GALNT17
    nsv5951025insertion1nstd209human GRCh38 chr7: 71,204,026-71,204,026 , GRCh37.p13 chr7: 70,669,012-70,669,012 GALNT17
    nsv5949812insertion1nstd209human GRCh38 chr7: 71,272,976-71,272,976 , GRCh37.p13 chr7: 70,737,962-70,737,962 GALNT17
    nsv5948002insertion1nstd209human GRCh38 chr7: 71,179,624-71,179,624 , GRCh37.p13 chr7: 70,644,610-70,644,610 GALNT17
    nsv5924446copy number variation1nstd209human GRCh38 chr7: 71,596,245-71,597,245 , GRCh37.p13 chr7: 71,061,230-71,062,230 GALNT17
    nsv5922486copy number variation1nstd209human GRCh38 chr7: 71,288,007-71,288,170 , GRCh37.p13 chr7: 70,752,993-70,753,156 GALNT17
    nsv5922246copy number variation1nstd209human GRCh38 chr7: 71,680,641-71,680,705 , GRCh37.p13 chr7: 71,145,626-71,145,690 GALNT17
    nsv5921754copy number variation1nstd209human GRCh38 chr7: 71,435,752-71,436,451 , GRCh37.p13 chr7: 70,900,737-70,901,436 GALNT17
    nsv5919932copy number variation1nstd209human GRCh38 chr7: 71,356,837-71,359,638 , GRCh37.p13 chr7: 70,821,823-70,824,624 GALNT17
    nsv5919312copy number variation1nstd209human GRCh38 chr7: 71,141,903-71,142,058 , GRCh37.p13 chr7: 70,606,889-70,607,044 GALNT17
    nsv5918891copy number variation1nstd209human GRCh38 chr7: 71,592,506-75,175,408 , GRCh37.p13 chr7|NW_003871064.1: 1-2,704,644 , GRCh37.p13 chr7: 71,935,722-74,527,751 , SPDYE10, 78 more genes
    nsv5918578copy number variation1nstd209human GRCh38 chr7: 71,158,429-71,158,610 , GRCh37.p13 chr7: 70,623,415-70,623,596 GALNT17
    nsv5916926copy number variation1nstd209human GRCh38 chr7: 71,501,896-71,501,964 , GRCh37.p13 chr7: 70,966,881-70,966,949 GALNT17
    nsv5915554copy number variation1nstd209human GRCh38 chr7: 71,544,379-71,545,588 , GRCh37.p13 chr7: 71,009,364-71,010,573 GALNT17
    nsv5915042copy number variation1nstd209human GRCh38 chr7: 71,604,174-71,604,248 , GRCh37.p13 chr7: 71,069,159-71,069,233 GALNT17
    nsv5914951copy number variation1nstd209human GRCh38 chr7: 71,154,726-71,159,930 , GRCh37.p13 chr7: 70,619,712-70,624,916 GALNT17
    nsv5910327copy number variation1nstd209human GRCh38 chr7: 71,376,149-71,376,277 , GRCh37.p13 chr7: 70,841,135-70,841,263 GALNT17
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