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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968604inversion1nstd209human GRCh38 chr2: 49,436,021-59,087,697 , GRCh37.p13 chr2: 49,663,159-59,314,832 , ACYP2, 95 more genes
    nsv5833660copy number variation1nstd209human GRCh38 chr2: 58,211,370-58,213,569 , GRCh37.p13 chr2: 58,438,505-58,440,704 FANCL
    nsv5833334copy number variation1nstd209human GRCh38 chr2: 58,174,731-58,177,843 , GRCh37.p13 chr2: 58,401,866-58,404,978 FANCL
    nsv5688037mobile element insertion2nstd211human GRCh38 chr2: 58,209,187-58,209,187 , GRCh37.p13 chr2: 58,436,322-58,436,322 FANCL
    nsv5679948mobile element insertion1nstd211human GRCh38 chr2: 58,184,620-58,184,620 , GRCh37.p13 chr2: 58,411,755-58,411,755 FANCL
    nsv5622840insertion1nstd207human GRCh38 chr2: 58,184,599-58,184,599 , GRCh37.p13 chr2: 58,411,734-58,411,734 FANCL
    nsv5573847copy number variation1nstd207human GRCh38 chr2: 58,217,142-58,217,192 , GRCh37.p13 chr2: 58,444,277-58,444,327 FANCL
    nsv5568405copy number variation1nstd207human GRCh38 chr2: 58,217,129-58,220,081 , GRCh37.p13 chr2: 58,444,264-58,447,216 FANCL
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5453748copy number variation1nstd206human GRCh38 chr2: 58,177,421-58,180,359 , GRCh37.p13 chr2: 58,404,556-58,407,494 FANCL
    nsv5446414copy number variation1nstd206human GRCh38 chr2: 58,236,302-58,236,405 , GRCh37.p13 chr2: 58,463,437-58,463,540 FANCL
    nsv5441799copy number variation1nstd206human GRCh38 chr2: 58,228,846-58,230,746 , GRCh37.p13 chr2: 58,455,981-58,457,881 FANCL
    nsv5439252copy number variation1nstd206human GRCh38 chr2: 58,217,131-58,220,082 , GRCh37.p13 chr2: 58,444,266-58,447,217 FANCL
    nsv5407766mobile element insertion1nstd206human GRCh38 chr2: 58,184,620-58,184,671 , GRCh37.p13 chr2: 58,411,755-58,411,806 FANCL
    nsv5404497mobile element insertion1nstd206human GRCh38 chr2: 58,209,187-58,209,238 , GRCh37.p13 chr2: 58,436,322-58,436,373 FANCL
    nsv5360340translocation1nstd200human GRCh38 chr2: 58,220,082-58,220,082 , GRCh38 chr2: 58,217,131-58,217,131 , GRCh37.p13 chr2: 58,444,266-58,444,266 , GRCh37.p13 chr2: 58,447,217-58,447,217 FANCL
    nsv5335930translocation1nstd200human GRCh37 chr2: 58,444,266-58,444,266 , GRCh37 chr2: 58,447,217-58,447,217 , GRCh38.p12 chr2: 58,220,082-58,220,082 , GRCh38.p12 chr2: 58,217,131-58,217,131 FANCL
    nsv5296127copy number variation1nstd204human GRCh38.p13 chr2: 58,188,026-58,188,190 , GRCh37.p13 chr2: 58,415,161-58,415,325 FANCL
    nsv5213832copy number variation1nstd204human GRCh38.p13 chr2: 58,189,501-58,194,000 , GRCh37.p13 chr2: 58,416,636-58,421,135 FANCL
    nsv5203148copy number variation1nstd204human GRCh38.p13 chr2: 58,221,301-58,226,500 , GRCh37.p13 chr2: 58,448,436-58,453,635 FANCL
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