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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5886414copy number variation1nstd209human GRCh38 chr1: 61,656,290-61,656,602 , GRCh37.p13 chr1: 62,121,962-62,122,274 MGC34796
    nsv5874980copy number variation1nstd209human GRCh38 chr1: 61,647,741-61,653,847 , GRCh37.p13 chr1: 62,113,413-62,119,519 LOC107984964, MGC34796
    nsv5830387copy number variation1nstd209human GRCh38 chr1: 61,647,704-61,653,803 , GRCh37.p13 chr1: 62,113,376-62,119,475 LOC107984964, MGC34796
    nsv5572029copy number variation1nstd207human GRCh38 chr1: 61,647,741-61,653,847 , GRCh37.p13 chr1: 62,113,413-62,119,519 MGC34796, LOC107984964
    nsv5429600copy number variation1nstd206human GRCh38 chr1: 61,647,742-61,653,848 , GRCh37.p13 chr1: 62,113,414-62,119,520 MGC34796, LOC107984964
    nsv5283136copy number variation1nstd204human GRCh37.p13 chr1: 62,113,414-62,119,520 , GRCh38.p13 chr1: 61,647,742-61,653,848 LOC107984964, MGC34796
    nsv5218956copy number variation1nstd204human GRCh38.p13 chr1: 61,645,801-61,655,400 , GRCh37.p13 chr1: 62,111,473-62,121,072 LOC107984964, MGC34796
    nsv5203702copy number variation1nstd204human GRCh38.p13 chr1: 61,647,692-61,653,703 , GRCh37.p13 chr1: 62,113,364-62,119,375 LOC107984964, MGC34796
    nsv5203206copy number variation1nstd204human GRCh38.p13 chr1: 61,652,701-61,653,700 , GRCh37.p13 chr1: 62,118,373-62,119,372 MGC34796
    nsv5063676mobile element insertion1nstd203human GRCh38 chr1: 61,656,555-61,656,595 , GRCh37.p13 chr1: 62,122,227-62,122,267 MGC34796
    nsv4890466copy number variation1nstd200human GRCh38 chr1: 61,651,901-61,669,959 , GRCh37.p13 chr1: 62,117,573-62,135,631 MGC34796
    nsv4890463copy number variation1nstd200human GRCh38 chr1: 61,647,742-61,653,848 , GRCh37.p13 chr1: 62,113,414-62,119,520 LOC107984964, MGC34796
    nsv4888344inversion1nstd200human GRCh37 chr1: 51,769,169-94,478,994 , GRCh38.p12 chr1: 51,303,497-94,013,438 , ST13P20, 664 more genes
    nsv4783435copy number variation1nstd200human GRCh37 chr1: 62,117,573-62,135,631 , GRCh38.p12 chr1: 61,651,901-61,669,959 MGC34796
    nsv4783433copy number variation1nstd200human GRCh37 chr1: 62,113,414-62,119,520 , GRCh38.p12 chr1: 61,647,742-61,653,848 LOC107984964, MGC34796
    nsv4768338copy number variation1nstd102humanPathogenic GRCh37 chr1: 53,675,707-66,644,963 , GRCh38.p12 chr1: 53,210,035-66,179,280 TALDO1P1, LAMTOR5P1, 201 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4743274copy number variation1nstd199human GRCh37 chr1: 62,113,414-62,119,521 , GRCh38.p12 chr1: 61,647,742-61,653,849 MGC34796, LOC107984964
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