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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053197inversion1nstd229human GRCh38 chr7: 72,920,579-74,172,062 , GRCh37.p13 chr7: 72,391,116-73,586,392 , GRCh37.p13 chr7|NW_003871064.1: 449,815-1,701,298 FKBP6, TRIM74, 41 more genes
    nsv6836076copy number variation1nstd229human GRCh38 chr7: 72,363,240-72,976,097 , GRCh37.p13 chr7: 71,935,722-72,446,627 , GRCh37.p13 chr7|NW_003871064.1: 1-505,333 POM121, SBDSP1, 10 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6632373copy number variation1nstd224human GRCh37 chr7: 72,313,144-72,761,178 , GRCh38.p12 chr7: 72,842,566-73,347,179 POM121, TRIM74, 20 more genes
    nsv6614783copy number variation1nstd223human GRCh38 chr7: 72,947,701-72,950,600 , GRCh37.p13 chr7|NW_003871064.1: 476,937-479,836 , GRCh37.p13 chr7: 72,418,240-72,421,139 POM121, NSUN5P2
    nsv6605284copy number variation1nstd223human GRCh38 chr7: 72,942,701-72,950,600 , GRCh37.p13 chr7|NW_003871064.1: 471,937-479,836 , GRCh37.p13 chr7: 72,413,240-72,421,139 POM121, NSUN5P2
    nsv6574642inversion1nstd223human GRCh38 chr7: 72,920,579-74,172,062 , GRCh37.p13 chr7|NW_003871064.1: 449,815-1,701,298 , GRCh37.p13 chr7: 72,391,116-73,586,392 CLDN4, TBL2, 41 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6142561copy number variation1nstd206human GRCh38 chr7: 72,942,389-73,297,889 , GRCh37.p13 chr7|NW_003871064.1: 471,625-827,125 POM121, GTF2IRD2P1, 15 more genes
    nsv6142507copy number variation1nstd206human GRCh37.p13 chr7|NW_003871064.1: 476,925-525,015 , GRCh38 chr7: 72,947,689-72,995,779 , GRCh37.p13 chr7: 72,418,228-72,466,308 POM121, STAG3L3, 3 more genes
    nsv6142088copy number variation1nstd206human GRCh38 chr7: 72,941,739-72,950,779 , GRCh37.p13 chr7|NW_003871064.1: 470,975-480,015 , GRCh37.p13 chr7: 72,412,278-72,421,318 POM121, NSUN5P2
    nsv6141969copy number variation1nstd206human GRCh37.p13 chr7|NW_003871064.1: 471,015-487,015 , GRCh38 chr7: 72,941,779-72,957,779 , GRCh37.p13 chr7: 72,412,318-72,428,310 TRIM74, POM121, 1 more genes
    nsv6141945copy number variation1nstd206human GRCh38 chr7: 72,954,779-72,960,779 , GRCh37.p13 chr7: 72,425,318-72,431,310 , GRCh37.p13 chr7|NW_003871064.1: 484,015-490,015 TRIM74, NSUN5P2
    nsv6141807copy number variation1nstd206human GRCh38 chr7: 72,698,779-73,300,779 , GRCh37.p13 chr7|NW_003871064.1: 228,028-830,015 PMS2P6, TYW1B, 22 more genes
    nsv6136261copy number variation1nstd213human GRCh37 chr7: 70,600,000-72,480,001 , GRCh38.p12 chr7: 71,135,014-73,009,480 SPDYE7P, STAG3L3, 19 more genes
    nsv5974071inversion1nstd209human GRCh37.p13 chr7|NW_003871064.1: 478,880-2,946,547 , GRCh38 chr7: 72,949,644-75,417,311 , CLDN4, 79 more genes
    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
    nsv5858570copy number variation2nstd209human GRCh38 chr7: 72,944,399-72,946,766 , GRCh37.p13 chr7|NW_003871064.1: 473,635-476,002 , GRCh37.p13 chr7: 72,414,938-72,417,305 POM121, NSUN5P2
    nsv5848290copy number variation2nstd209human GRCh38 chr7: 72,947,474-72,950,387 , GRCh37.p13 chr7|NW_003871064.1: 476,710-479,623 , GRCh37.p13 chr7: 72,418,013-72,420,926 NSUN5P2, POM121
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
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