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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969697inversion1nstd209human GRCh38 chr7: 32,901,386-32,945,048 , GRCh37.p13 chr7: 32,940,998-32,984,660 RP9P
    nsv5958135insertion1nstd209human GRCh38 chr7: 32,935,030-32,935,030 , GRCh37.p13 chr7: 32,974,642-32,974,642 RP9P
    nsv5919512copy number variation1nstd209human GRCh38 chr7: 26,509,679-33,120,288 , GRCh37.p13 chr7: 26,549,298-33,159,900 , CPVL-AS1, 126 more genes
    nsv5918668copy number variation1nstd209human GRCh38 chr7: 32,782,611-34,873,019 , GRCh37.p13 chr7: 32,822,223-34,912,631 KBTBD2, NPSR1, 18 more genes
    nsv5914132copy number variation1nstd209human GRCh38 chr7: 26,936,027-36,716,695 , GRCh37.p13 chr7: 26,975,646-36,756,300 , HOXA7, 162 more genes
    nsv5846938copy number variation1nstd209human GRCh38 chr7: 32,938,852-32,944,500 , GRCh37.p13 chr7: 32,978,464-32,984,112 RP9P
    nsv5635310insertion1nstd207human GRCh38 chr7: 32,935,030-32,935,030 , GRCh37.p13 chr7: 32,974,642-32,974,642 RP9P
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5378647translocation1nstd200human GRCh38 chr7: 32,920,951-32,920,951 , GRCh38 chr7: 32,921,029-32,921,029 , GRCh37.p13 chr7: 32,960,641-32,960,641 , GRCh37.p13 chr7: 32,960,563-32,960,563 RP9P
    nsv5040435inversion1nstd200human GRCh38 chr7: 32,354,819-33,704,107 , GRCh37.p13 chr7: 32,394,431-33,743,719 DPY19L1P1, DPY19L1P2, 20 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4956294copy number variation1nstd200human GRCh38 chr7: 32,940,836-32,945,737 , GRCh37.p13 chr7: 32,980,448-32,985,349 RP9P
    nsv4956293copy number variation1nstd200human GRCh38 chr7: 32,940,742-32,951,466 , GRCh37.p13 chr7: 32,980,354-32,991,078 RP9P
    nsv4953565copy number variation1nstd200human GRCh38 chr7: 32,938,622-32,944,768 , GRCh37.p13 chr7: 32,978,234-32,984,380 RP9P
    nsv4953564copy number variation1nstd200human GRCh38 chr7: 32,935,038-32,936,197 , GRCh37.p13 chr7: 32,974,650-32,975,809 RP9P
    nsv4953563copy number variation1nstd200human GRCh38 chr7: 32,933,610-32,934,630 , GRCh37.p13 chr7: 32,973,222-32,974,242 RP9P
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4811272copy number variation1nstd200human GRCh37 chr7: 32,980,448-32,985,349 , GRCh38.p12 chr7: 32,940,836-32,945,737 RP9P
    nsv4753816insertion1nstd199human GRCh37 chr7: 32,974,610-32,974,610 , GRCh38.p12 chr7: 32,934,998-32,934,998 RP9P
    nsv4674822copy number variation1nstd102humanPathogenic GRCh37 chr7: 23,877,135-33,139,446 , GRCh38.p12 chr7: 23,837,516-33,099,834 RP9P, LINC00997, 156 more genes
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