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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116511mobile element insertion1nstd186human GRCh37 chr13: 31,892,029-31,892,029 , GRCh38.p12 chr13: 31,317,892-31,317,892 B3GLCT
    nsv6112810copy number variation1nstd102humanPathogenic GRCh37 chr13: 28,925,153-34,061,696 , GRCh38.p12 chr13: 28,351,016-33,487,559 MTUS2, ALOX5AP, 70 more genes
    nsv5979982insertion1nstd209human GRCh38 chr13: 31,298,354-31,298,354 , GRCh37.p13 chr13: 31,872,491-31,872,491 B3GLCT
    nsv5968025insertion1nstd209human GRCh38 chr13: 31,317,892-31,317,892 , GRCh37.p13 chr13: 31,892,029-31,892,029 B3GLCT
    nsv5937118copy number variation1nstd209human GRCh38 chr13: 31,212,533-31,212,669 , GRCh37.p13 chr13: 31,786,670-31,786,806 B3GLCT
    nsv5931769copy number variation1nstd209human GRCh38 chr13: 31,216,384-31,216,441 , GRCh37.p13 chr13: 31,790,521-31,790,578 B3GLCT
    nsv5928095copy number variation1nstd209human GRCh38 chr13: 31,215,145-31,216,011 , GRCh37.p13 chr13: 31,789,282-31,790,148 B3GLCT
    nsv5705478mobile element insertion1nstd211human GRCh38 chr13: 31,236,810-31,236,810 , GRCh37.p13 chr13: 31,810,947-31,810,947 B3GLCT
    nsv5705433mobile element insertion2nstd211human GRCh38 chr13: 31,317,908-31,317,908 , GRCh37.p13 chr13: 31,892,045-31,892,045 B3GLCT
    nsv5645908insertion1nstd207human GRCh38 chr13: 31,317,892-31,317,892 , GRCh37.p13 chr13: 31,892,029-31,892,029 B3GLCT
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5505180copy number variation1nstd206human GRCh38 chr13: 31,297,207-31,297,258 , GRCh37.p13 chr13: 31,871,344-31,871,395 B3GLCT
    nsv5501707copy number variation1nstd206human GRCh38 chr13: 31,151,681-31,314,087 , GRCh37.p13 chr13: 31,725,818-31,888,224 HSPH1, LOC105370148, 2 more genes
    nsv5432579mobile element insertion1nstd206human GRCh38 chr13: 31,236,810-31,236,861 , GRCh37.p13 chr13: 31,810,947-31,810,998 B3GLCT
    nsv5414865mobile element insertion1nstd206human GRCh38 chr13: 31,317,892-31,317,892 , GRCh37.p13 chr13: 31,892,029-31,892,029 B3GLCT
    nsv5374130translocation1nstd200human GRCh38 chr13: 31,624,595-31,624,595 , GRCh38 chr13: 31,331,412-31,331,412 , GRCh37.p13 chr13: 31,905,549-31,905,549 , GRCh37.p13 chr13: 32,198,732-32,198,732 B3GLCT
    nsv5342115translocation1nstd200human GRCh37 chr13: 31,905,549-31,905,549 , GRCh37 chr13: 32,198,732-32,198,732 , GRCh38.p12 chr13: 31,331,412-31,331,412 , GRCh38.p12 chr13: 31,624,595-31,624,595 B3GLCT
    nsv5304778copy number variation1nstd204human GRCh38.p13 chr13: 31,249,834-31,250,000 , GRCh37.p13 chr13: 31,823,971-31,824,137 B3GLCT
    nsv5191566mobile element insertion1nstd203human GRCh38 chr13: 31,253,595-31,253,621 , GRCh37.p13 chr13: 31,827,732-31,827,758 B3GLCT
    nsv5157260mobile element insertion1nstd203human GRCh38 chr13: 31,317,897-31,317,908 , GRCh37.p13 chr13: 31,892,034-31,892,045 B3GLCT
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