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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7046578inversion1nstd229human GRCh38 chr7: 35,433,834-36,167,539 , GRCh37.p13 chr7: 35,473,444-36,207,148 HERPUD2, LOC101928421, 16 more genes
    nsv7045806inversion1nstd229human GRCh38 chr7: 35,074,085-37,751,599 , GRCh37.p13 chr7: 35,113,697-37,791,201 RNU6-565P, SEPTIN7, 36 more genes
    nsv7045327inversion1nstd229human GRCh38 chr7: 34,817,999-37,653,204 , GRCh37.p13 chr7: 34,857,611-37,692,807 ELMO1-AS1, DPY19L2P1, 40 more genes
    nsv6824236copy number variation1nstd229human GRCh38 chr7: 35,686,901-35,719,200 , GRCh37.p13 chr7: 35,726,511-35,758,810 HERPUD2-AS1, LINC03013, 1 more genes
    nsv6821941copy number variation1nstd229human GRCh38 chr7: 35,708,745-35,715,718 , GRCh37.p13 chr7: 35,748,355-35,755,328 LINC03013
    nsv6821049copy number variation1nstd229human GRCh38 chr7: 35,712,551-35,722,157 , GRCh37.p13 chr7: 35,752,161-35,761,767 LINC03013
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6561099inversion1nstd223human GRCh38 chr7: 35,676,182-35,775,356 , GRCh37.p13 chr7: 35,715,792-35,814,966 HERPUD2, LOC442293, 3 more genes
    nsv6559554inversion1nstd223human GRCh38 chr7: 34,818,072-37,653,201 , GRCh37.p13 chr7: 34,857,684-37,692,804 LOC105375233, LOC107986734, 40 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313670copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 27,507,832-39,072,473 , GRCh38.p12 chr7: 27,468,213-39,032,873 ADCYAP1R1, AMPH, 175 more genes
    nsv6136990copy number variation1nstd213human GRCh37 chr7: 34,800,000-36,730,001 , GRCh38.p12 chr7: 34,760,388-36,690,396 EEPD1, NPSR1, 31 more genes
    nsv5975022inversion1nstd209human GRCh38 chr7: 34,818,028-37,653,165 , GRCh37.p13 chr7: 34,857,640-37,692,768 , AOAH, 41 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
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4966173copy number variation1nstd200human GRCh38 chr7: 35,708,740-35,715,716 , GRCh37.p13 chr7: 35,748,350-35,755,326 LINC03013
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4811314copy number variation1nstd200human GRCh37 chr7: 35,748,350-35,755,326 , GRCh38.p12 chr7: 35,708,740-35,715,716 LINC03013
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
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