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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905557copy number variation1nstd209human GRCh38 chr2: 241,956,264-242,012,194 , GRCh37.p13 chr2: 242,898,415-242,954,345 LOC285097, LINC01237, 1 more genes
    nsv5896661copy number variation1nstd209human GRCh38 chr2: 241,977,163-242,009,356 , GRCh37.p13 chr2: 242,919,314-242,951,507 LOC285097, LINC01237, 1 more genes
    nsv5892750copy number variation1nstd209human GRCh38 chr2: 241,911,101-242,093,626 , GRCh37.p13 chr2: 242,853,252-243,035,777 LOC285097, LINC01881, 4 more genes
    nsv5892278copy number variation1nstd209human GRCh38 chr2: 241,955,739-241,994,594 , GRCh37.p13 chr2: 242,897,890-242,936,745 LINC01237, LINC01238
    nsv5889512copy number variation1nstd209human GRCh38 chr2: 241,977,163-242,010,029 , GRCh37.p13 chr2: 242,919,314-242,952,180 LOC285097, LINC01237, 1 more genes
    nsv5833137copy number variation2nstd209human GRCh38 chr2: 241,976,918-241,985,626 , GRCh37.p13 chr2: 242,919,069-242,927,777 LINC01237, LINC01238
    nsv5832915copy number variation1nstd209human GRCh38 chr2: 241,953,581-241,969,717 , GRCh37.p13 chr2: 242,895,732-242,911,868 LINC01237, LINC01238
    nsv5832837copy number variation2nstd209human GRCh38 chr2: 241,973,893-241,996,982 , GRCh37.p13 chr2: 242,916,044-242,939,133 LINC01237, LINC01238
    nsv5832836copy number variation2nstd209human GRCh38 chr2: 241,964,866-241,975,317 , GRCh37.p13 chr2: 242,907,017-242,917,468 LINC01237, LINC01238
    nsv5832276copy number variation1nstd209human GRCh38 chr2: 241,969,218-241,975,917 , GRCh37.p13 chr2: 242,911,369-242,918,068 LINC01238, LINC01237
    nsv5619491insertion1nstd207human GRCh38 chr2: 241,968,823-241,968,823 , GRCh37.p13 chr2: 242,910,974-242,910,974 LINC01238, LINC01237
    nsv5614283insertion1nstd207human GRCh38 chr2: 241,968,875-241,968,875 , GRCh37.p13 chr2: 242,911,026-242,911,026 LINC01238, LINC01237
    nsv5607175insertion1nstd207human GRCh38 chr2: 241,975,383-241,975,383 , GRCh37.p13 chr2: 242,917,534-242,917,534 LINC01238, LINC01237
    nsv5583451copy number variation1nstd207human GRCh38 chr2: 241,977,163-242,008,978 , GRCh37.p13 chr2: 242,919,314-242,951,129 LOC285097, LINC01237, 1 more genes
    nsv5573231copy number variation1nstd207human GRCh38 chr2: 241,968,718-241,968,795 , GRCh37.p13 chr2: 242,910,869-242,910,946 LINC01238, LINC01237
    nsv5441586copy number variation1nstd206human GRCh38 chr2: 241,947,461-241,982,356 , GRCh37.p13 chr2: 242,889,612-242,924,507 LINC01237, LINC01238
    nsv5439052copy number variation1nstd206human GRCh38 chr2: 241,955,741-241,994,595 , GRCh37.p13 chr2: 242,897,892-242,936,746 LINC01237, LINC01238
    nsv5381323copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,201,756-243,048,760 , GRCh38.p12 chr2: 236,293,113-242,106,609 LRRFIP1, GPR35, 133 more genes
    nsv5366926translocation1nstd200human GRCh38 chr2: 242,022,424-242,022,424 , GRCh38 chr2: 241,975,578-241,975,578 , GRCh37.p13 chr2: 242,964,575-242,964,575 , GRCh37.p13 chr2: 242,917,729-242,917,729 LINC01238, LINC01237
    nsv5366925translocation1nstd200human GRCh38 chr2: 241,968,070-241,968,070 , GRCh38 chr2: 241,976,938-241,976,938 , GRCh37.p13 chr2: 242,919,089-242,919,089 , GRCh37.p13 chr2: 242,910,221-242,910,221 LINC01238, LINC01237
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