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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924274copy number variation1nstd209human GRCh38 chr7: 65,388,301-65,388,351 , GRCh37.p13 chr7: 64,853,214-64,853,264 ZNF92
    nsv5922394copy number variation1nstd209human GRCh38 chr7: 65,103,162-65,765,400 , GRCh37.p13 chr7: 64,563,540-65,012,082 , CCT6P1, 13 more genes
    nsv5920709copy number variation1nstd209human GRCh38 chr7: 65,106,549-65,795,958 , GRCh37.p13 chr7: 64,566,927-65,012,082 , LOC402279, 14 more genes
    nsv5918237copy number variation1nstd209human GRCh38 chr7: 65,186,338-65,692,583 , GRCh37.p13 chr7: 64,646,716-65,012,082 , LOC101929322, 10 more genes
    nsv5907866copy number variation1nstd209human GRCh38 chr7: 65,084,132-65,773,545 , GRCh37.p13 chr7: 64,544,510-65,012,082 , LOC101929322, 15 more genes
    nsv5847509copy number variation2nstd209human GRCh38 chr7: 65,351,935-65,372,781 , GRCh37.p13 chr7: 64,816,848-64,837,694 ZNF92, LOC100533634
    nsv5847451copy number variation2nstd209human GRCh38 chr7: 65,392,157-65,397,782 , GRCh37.p13 chr7: 64,857,070-64,862,695 ZNF92
    nsv5667919inversion1nstd207human GRCh37.p13 chr7: 64,679,536-65,012,082 , GRCh38 chr7: 65,219,158-65,629,739 , ZNF92, 8 more genes
    nsv5584460copy number variation1nstd207human GRCh38 chr7: 65,388,301-65,388,351 , GRCh37.p13 chr7: 64,853,214-64,853,264 ZNF92
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5493290copy number variation1nstd206human GRCh38 chr7: 65,388,302-65,388,352 , GRCh37.p13 chr7: 64,853,215-64,853,265 ZNF92
    nsv5487423copy number variation1nstd206human GRCh38 chr7: 65,116,779-65,658,779 , GRCh37.p13 chr7: 64,577,157-65,012,082 , LOC402279, 10 more genes
    nsv5484655copy number variation1nstd206human GRCh37.p13 chr7|NW_004775430.1: 1-200,121 , GRCh38 chr7: 65,364,562-65,747,290 , GRCh37.p13 chr7: 65,011,979-65,212,277 , ZNF92, 4 more genes
    nsv5483447copy number variation1nstd206human GRCh38 chr7: 65,106,779-65,664,989 , GRCh37.p13 chr7: 64,567,157-65,012,082 , LOC101929322, 10 more genes
    nsv5370469translocation1nstd200human GRCh38 chr7: 26,948,620-26,948,620 , GRCh38 chr7: 65,395,073-65,395,073 , GRCh37.p13 chr7: 26,988,239-26,988,239 , GRCh37.p13 chr7: 64,859,986-64,859,986 ZNF92
    nsv5363784translocation1nstd200human GRCh38 chr7: 65,386,717-65,386,717 , GRCh38 chr7: 65,385,888-65,385,888 , GRCh37.p13 chr7: 64,851,630-64,851,630 , GRCh37.p13 chr7: 64,850,801-64,850,801 ZNF92
    nsv5334014translocation1nstd200human GRCh37 chr7: 26,988,239-26,988,239 , GRCh37 chr7: 64,859,986-64,859,986 , GRCh38.p12 chr7: 26,948,620-26,948,620 , GRCh38.p12 chr7: 65,395,073-65,395,073 ZNF92
    nsv5233440copy number variation1nstd204human GRCh38.p13 chr7: 65,398,169-65,399,368 , GRCh37.p13 chr7: 64,863,082-64,864,281 ZNF92
    nsv5230373copy number variation1nstd204human GRCh38.p13 chr7: 65,324,526-65,371,881 , GRCh37.p13 chr7: 64,789,439-64,836,794 LOC100533634, RSL24D1P3, 2 more genes
    nsv5224091copy number variation1nstd204human GRCh38.p13 chr7: 65,386,582-65,388,706 , GRCh37.p13 chr7: 64,851,495-64,853,619 ZNF92
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