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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114991mobile element insertion1nstd186human GRCh37 chr12: 107,122,075-107,122,075 , GRCh38.p12 chr12: 106,728,297-106,728,297 LOC100287944, RFX4
    nsv5970232insertion1nstd209human GRCh38 chr12: 106,728,297-106,728,297 , GRCh37.p13 chr12: 107,122,075-107,122,075 RFX4, LOC100287944
    nsv5944950copy number variation1nstd209human GRCh38 chr12: 106,760,732-106,761,134 , GRCh37.p13 chr12: 107,154,510-107,154,912 RFX4, LOC100287944
    nsv5942380copy number variation1nstd209human GRCh38 chr12: 106,613,183-106,613,258 , GRCh37.p13 chr12: 107,006,961-107,007,036 RFX4, LOC100287944
    nsv5939492copy number variation1nstd209human GRCh38 chr12: 106,620,539-106,620,588 , GRCh37.p13 chr12: 107,014,317-107,014,366 LOC100287944, RFX4
    nsv5697320mobile element insertion2nstd211human GRCh38 chr12: 106,728,308-106,728,308 , GRCh37.p13 chr12: 107,122,086-107,122,086 LOC100287944, RFX4
    nsv5696240mobile element insertion1nstd211human GRCh38 chr12: 106,737,656-106,737,656 , GRCh37.p13 chr12: 107,131,434-107,131,434 RFX4, LOC100287944
    nsv5663812insertion1nstd207human GRCh38 chr12: 106,623,595-106,623,595 , GRCh37.p13 chr12: 107,017,373-107,017,373 RFX4, LOC100287944
    nsv5647898insertion1nstd207human GRCh38 chr12: 106,728,297-106,728,297 , GRCh37.p13 chr12: 107,122,075-107,122,075 LOC100287944, RFX4
    nsv5556177sequence alteration1nstd206human GRCh38 chr12: 106,608,104-106,608,104 , GRCh37.p13 chr12: 107,001,882-107,001,882 RFX4, LOC100287944
    nsv5510384copy number variation1nstd206human GRCh38 chr12: 106,670,589-106,670,745 , GRCh37.p13 chr12: 107,064,367-107,064,523 LOC100287944, RFX4
    nsv5509286copy number variation1nstd206human GRCh38 chr12: 106,700,397-106,700,705 , GRCh37.p13 chr12: 107,094,175-107,094,483 RFX4, LOC100287944
    nsv5506827copy number variation1nstd206human GRCh38 chr12: 106,613,728-106,614,013 , GRCh37.p13 chr12: 107,007,506-107,007,791 RFX4, LOC100287944
    nsv5504031copy number variation1nstd206human GRCh38 chr12: 106,760,732-106,761,135 , GRCh37.p13 chr12: 107,154,510-107,154,913 LOC100287944, RFX4
    nsv5497876copy number variation1nstd206human GRCh38 chr12: 106,601,200-106,601,270 , GRCh37.p13 chr12: 106,994,978-106,995,048 RFX4, LOC100287944
    nsv5427965mobile element insertion1nstd206human GRCh38 chr12: 106,737,656-106,737,707 , GRCh37.p13 chr12: 107,131,434-107,131,485 RFX4, LOC100287944
    nsv5427591mobile element insertion1nstd206human GRCh38 chr12: 106,728,297-106,728,297 , GRCh37.p13 chr12: 107,122,075-107,122,075 LOC100287944, RFX4
    nsv5356347translocation1nstd200human GRCh38 chr12: 106,760,732-106,760,732 , GRCh38 chr12: 106,761,135-106,761,135 , GRCh37.p13 chr12: 107,154,510-107,154,510 , GRCh37.p13 chr12: 107,154,913-107,154,913 RFX4, LOC100287944
    nsv5356346translocation1nstd200human GRCh38 chr12: 106,688,150-106,688,150 , GRCh38 chr12: 106,688,064-106,688,064 , GRCh37.p13 chr12: 107,081,842-107,081,842 , GRCh37.p13 chr12: 107,081,928-107,081,928 RFX4, LOC100287944
    nsv5356345translocation1nstd200human GRCh38 chr12: 106,644,932-106,644,932 , GRCh38 chr12: 106,644,834-106,644,834 , GRCh37.p13 chr12: 107,038,612-107,038,612 , GRCh37.p13 chr12: 107,038,710-107,038,710 RFX4, LOC100287944
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