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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958717insertion1nstd209human GRCh38 chr2: 213,112,342-213,112,342 , GRCh37.p13 chr2: 213,977,066-213,977,066 IKZF2
    nsv5904444copy number variation1nstd209human GRCh38 chr2: 213,133,510-213,135,465 , GRCh37.p13 chr2: 213,998,234-214,000,189 IKZF2
    nsv5832490copy number variation1nstd209human GRCh38 chr2: 213,036,684-213,038,176 , GRCh37.p13 chr2: 213,901,408-213,902,900 IKZF2
    nsv5832447copy number variation1nstd209human GRCh38 chr2: 213,133,635-213,135,553 , GRCh37.p13 chr2: 213,998,359-214,000,277 IKZF2
    nsv5686489mobile element insertion2nstd211human GRCh38 chr2: 213,085,465-213,085,465 , GRCh37.p13 chr2: 213,950,189-213,950,189 IKZF2
    nsv5680520mobile element insertion2nstd211human GRCh38 chr2: 213,112,358-213,112,358 , GRCh37.p13 chr2: 213,977,082-213,977,082 IKZF2
    nsv5615849insertion1nstd207human GRCh38 chr2: 213,112,342-213,112,342 , GRCh37.p13 chr2: 213,977,066-213,977,066 IKZF2
    nsv5560850sequence alteration1nstd206human GRCh38 chr2: 213,059,481-213,059,485 , GRCh37.p13 chr2: 213,924,205-213,924,209 IKZF2
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5552803insertion1nstd206human GRCh38 chr2: 213,059,481-213,059,481 , GRCh37.p13 chr2: 213,924,205-213,924,205 IKZF2
    nsv5446752copy number variation1nstd206human GRCh38 chr2: 213,132,239-213,135,463 , GRCh37.p13 chr2: 213,996,963-214,000,187 IKZF2
    nsv5446377copy number variation1nstd206human GRCh38 chr2: 213,005,125-213,005,444 , GRCh37.p13 chr2: 213,869,849-213,870,168 IKZF2
    nsv5401276mobile element insertion1nstd206human GRCh38 chr2: 213,112,342-213,112,342 , GRCh37.p13 chr2: 213,977,066-213,977,066 IKZF2
    nsv5400369mobile element insertion1nstd206human GRCh38 chr2: 213,085,453-213,085,453 , GRCh37.p13 chr2: 213,950,177-213,950,177 IKZF2
    nsv5366815translocation1nstd200human GRCh38 chr2: 213,124,240-213,124,240 , GRCh38 chr2: 213,124,334-213,124,334 , GRCh37.p13 chr2: 213,989,058-213,989,058 , GRCh37.p13 chr2: 213,988,964-213,988,964 IKZF2
    nsv5366814translocation1nstd200human GRCh38 chr13: 91,697,474-91,697,474 , GRCh38 chr2: 213,017,016-213,017,016 , GRCh37.p13 chr13: 92,349,728-92,349,728 , GRCh37.p13 chr2: 213,881,740-213,881,740 IKZF2, GPC5
    nsv5361272translocation1nstd200human GRCh38 chr2: 213,057,748-213,057,748 , GRCh38 chr2: 213,059,485-213,059,485 , GRCh37.p13 chr2: 213,924,209-213,924,209 , GRCh37.p13 chr2: 213,922,472-213,922,472 IKZF2
    nsv5361270translocation1nstd200human GRCh38 chr2: 213,005,444-213,005,444 , GRCh38 chr2: 213,005,125-213,005,125 , GRCh37.p13 chr2: 213,869,849-213,869,849 , GRCh37.p13 chr2: 213,870,168-213,870,168 IKZF2
    nsv5335488translocation1nstd200human GRCh37 chr2: 213,870,168-213,870,168 , GRCh37 chr2: 213,869,849-213,869,849 , GRCh38.p12 chr2: 213,005,125-213,005,125 , GRCh38.p12 chr2: 213,005,444-213,005,444 IKZF2
    nsv5216080copy number variation1nstd204human GRCh38.p13 chr2: 213,055,001-213,062,800 , GRCh37.p13 chr2: 213,919,725-213,927,524 IKZF2
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