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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130337insertion1nstd186human GRCh37 chr16: 47,327,131-47,327,143 , GRCh38.p12 chr16: 47,293,220-47,293,232 ITFG1
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5979505inversion1nstd209human GRCh38 chr16: 46,982,903-47,949,086 , GRCh37.p13 chr16: 47,016,814-47,982,997 PHKB, ITFG1, 13 more genes
    nsv5976918insertion1nstd209human GRCh38 chr16: 47,293,181-47,293,181 , GRCh37.p13 chr16: 47,327,092-47,327,092 ITFG1
    nsv5940657copy number variation1nstd209human GRCh38 chr16: 47,334,945-47,337,784 , GRCh37.p13 chr16: 47,368,856-47,371,695 ITFG1
    nsv5934628copy number variation1nstd209human GRCh38 chr16: 47,413,934-47,418,190 , GRCh37.p13 chr16: 47,447,845-47,452,101 ITFG1
    nsv5885586copy number variation1nstd209human GRCh38 chr16: 47,186,198-47,188,794 , GRCh37.p13 chr16: 47,220,109-47,222,705 ITFG1
    nsv5884387copy number variation1nstd209human GRCh38 chr16: 47,181,912-47,186,618 , GRCh37.p13 chr16: 47,215,823-47,220,529 ITFG1
    nsv5880899copy number variation1nstd209human GRCh38 chr16: 47,175,586-47,187,517 , GRCh37.p13 chr16: 47,209,497-47,221,428 ITFG1
    nsv5878055copy number variation1nstd209human GRCh38 chr16: 47,183,207-47,186,764 , GRCh37.p13 chr16: 47,217,118-47,220,675 ITFG1
    nsv5870298copy number variation1nstd209human GRCh38 chr16: 47,413,926-47,418,094 , GRCh37.p13 chr16: 47,447,837-47,452,005 ITFG1
    nsv5716897mobile element insertion1nstd211human GRCh38 chr16: 47,152,662-47,152,662 , GRCh37.p13 chr16: 47,186,573-47,186,573 ITFG1, ITFG1-AS1
    nsv5716872mobile element insertion2nstd211human GRCh38 chr16: 47,301,360-47,301,360 , GRCh37.p13 chr16: 47,335,271-47,335,271 ITFG1, LOC101927080
    nsv5713087mobile element insertion2nstd211human GRCh38 chr16: 47,424,691-47,424,691 , GRCh37.p13 chr16: 47,458,602-47,458,602 ITFG1
    nsv5712211mobile element insertion2nstd211human GRCh38 chr16: 47,428,971-47,428,971 , GRCh37.p13 chr16: 47,462,882-47,462,882 ITFG1
    nsv5710265mobile element insertion1nstd211human GRCh38 chr16: 47,213,208-47,213,208 , GRCh37.p13 chr16: 47,247,119-47,247,119 ITFG1
    nsv5708208mobile element insertion1nstd211human GRCh38 chr16: 47,322,985-47,322,985 , GRCh37.p13 chr16: 47,356,896-47,356,896 ITFG1
    nsv5697812mobile element insertion1nstd211human GRCh38 chr16: 47,433,299-47,433,299 , GRCh37.p13 chr16: 47,467,210-47,467,210 ITFG1
    nsv5659716insertion1nstd207human GRCh38 chr16: 47,305,942-47,305,942 , GRCh37.p13 chr16: 47,339,853-47,339,853 LOC101927080, ITFG1
    nsv5658413insertion1nstd207human GRCh38 chr16: 47,293,181-47,293,181 , GRCh37.p13 chr16: 47,327,092-47,327,092 ITFG1
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