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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963913insertion1nstd209human GRCh38 chr2: 219,072,653-219,072,653 , GRCh37.p13 chr2: 219,937,375-219,937,375 NHEJ1
    nsv5951258insertion1nstd209human GRCh38 chr2: 219,159,552-219,159,552 , GRCh37.p13 chr2: 220,024,274-220,024,274 NHEJ1, SLC23A3
    nsv5906723copy number variation1nstd209human GRCh38 chr2: 219,102,849-219,103,025 , GRCh37.p13 chr2: 219,967,571-219,967,747 RN7SL764P, NHEJ1
    nsv5620801insertion1nstd207human GRCh38 chr2: 219,080,589-219,080,589 , GRCh37.p13 chr2: 219,945,311-219,945,311 NHEJ1
    nsv5620643insertion1nstd207human GRCh38 chr2: 219,072,653-219,072,653 , GRCh37.p13 chr2: 219,937,375-219,937,375 NHEJ1
    nsv5607589insertion1nstd207human GRCh38 chr2: 219,159,552-219,159,552 , GRCh37.p13 chr2: 220,024,274-220,024,274 SLC23A3, NHEJ1
    nsv5605709insertion1nstd207human GRCh38 chr2: 219,141,379-219,141,379 , GRCh37.p13 chr2: 220,006,101-220,006,101 NHEJ1
    nsv5581798copy number variation1nstd207human GRCh38 chr2: 219,102,849-219,103,025 , GRCh37.p13 chr2: 219,967,571-219,967,747 RN7SL764P, NHEJ1
    nsv5573495copy number variation1nstd207human GRCh38 chr2: 219,159,514-219,159,575 , GRCh37.p13 chr2: 220,024,236-220,024,297 SLC23A3, NHEJ1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5552689insertion1nstd206human GRCh38 chr2: 219,072,667-219,072,704 , GRCh37.p13 chr2: 219,937,389-219,937,426 NHEJ1
    nsv5536160insertion1nstd206human GRCh38 chr2: 219,141,390-219,141,430 , GRCh37.p13 chr2: 220,006,112-220,006,152 NHEJ1
    nsv5450594copy number variation1nstd206human GRCh38 chr2: 219,159,535-219,159,589 , GRCh37.p13 chr2: 220,024,257-220,024,311 NHEJ1, SLC23A3
    nsv5384211copy number variation1nstd186human GRCh37 chr2: 219,931,898-219,932,166 , GRCh38.p12 chr2: 219,067,176-219,067,444 NHEJ1
    nsv5192617mobile element insertion1nstd203human GRCh38 chr2: 219,133,660-219,133,672 , GRCh37.p13 chr2: 219,998,382-219,998,394 NHEJ1
    nsv5071720mobile element insertion1nstd203human GRCh38 chr2: 219,100,871-219,100,887 , GRCh37.p13 chr2: 219,965,593-219,965,609 RN7SL764P, NHEJ1
    nsv5067916mobile element insertion1nstd203human GRCh38 chr2: 219,141,379-219,141,390 , GRCh37.p13 chr2: 220,006,101-220,006,112 NHEJ1
    nsv5029880inversion1nstd200human GRCh38 chr2: 213,444,845-219,177,092 , GRCh37.p13 chr2: 214,309,569-220,041,814 , LOC102724861, 122 more genes
    nsv4916926copy number variation1nstd200human GRCh38 chr2: 219,153,190-219,153,930 , GRCh37.p13 chr2: 220,017,912-220,018,652 NHEJ1
    nsv4916925copy number variation1nstd200human GRCh38 chr2: 219,137,534-219,137,599 , GRCh37.p13 chr2: 220,002,256-220,002,321 NHEJ1
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