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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976763inversion1nstd209human GRCh38 chr9: 33,796,601-33,979,181 , GRCh37.p13 chr9: 33,796,599-33,979,179 PRSS3, UBE2R2, 5 more genes
    nsv5960057insertion1nstd209human GRCh38 chr9: 34,035,514-34,035,514 , GRCh37.p13 chr9: 34,035,512-34,035,512 UBAP2
    nsv5956520insertion1nstd209human GRCh38 chr9: 33,969,654-33,969,654 , GRCh37.p13 chr9: 33,969,652-33,969,652 UBAP2
    nsv5911067copy number variation1nstd209human GRCh38 chr9: 34,027,572-34,030,014 , GRCh37.p13 chr9: 34,027,570-34,030,012 UBAP2
    nsv5910880copy number variation1nstd209human GRCh38 chr9: 34,037,759-34,037,820 , GRCh37.p13 chr9: 34,037,757-34,037,818 UBAP2
    nsv5866358copy number variation1nstd209human GRCh38 chr9: 34,036,187-34,037,962 , GRCh37.p13 chr9: 34,036,185-34,037,960 UBAP2
    nsv5865661copy number variation1nstd209human GRCh38 chr9: 34,027,628-34,029,961 , GRCh37.p13 chr9: 34,027,626-34,029,959 UBAP2
    nsv5860372copy number variation2nstd209human GRCh38 chr9: 33,995,330-33,996,731 , GRCh37.p13 chr9: 33,995,328-33,996,729 UBAP2
    nsv5852062copy number variation1nstd209human GRCh38 chr9: 34,037,388-34,038,888 , GRCh37.p13 chr9: 34,037,386-34,038,886 UBAP2
    nsv5714831mobile element insertion1nstd211human GRCh38 chr9: 33,990,461-33,990,461 , GRCh37.p13 chr9: 33,990,459-33,990,459 UBAP2
    nsv5713640mobile element insertion2nstd211human GRCh38 chr9: 33,933,673-33,933,673 , GRCh37.p13 chr9: 33,933,671-33,933,671 UBAP2, SNORD121B
    nsv5697121mobile element insertion2nstd211human GRCh38 chr9: 34,019,767-34,019,767 , GRCh37.p13 chr9: 34,019,765-34,019,765 UBAP2
    nsv5637183insertion1nstd207human GRCh38 chr9: 34,035,514-34,035,514 , GRCh37.p13 chr9: 34,035,512-34,035,512 UBAP2
    nsv5630132insertion2nstd207human GRCh38 chr9: 33,981,084-33,981,084 , GRCh37.p13 chr9: 33,981,082-33,981,082 UBAP2
    nsv5596534copy number variation1nstd207human GRCh38 chr9: 33,939,786-33,939,871 , GRCh37.p13 chr9: 33,939,784-33,939,869 UBAP2
    nsv5595122copy number variation1nstd207human GRCh38 chr9: 34,016,226-34,016,284 , GRCh37.p13 chr9: 34,016,224-34,016,282 RNU7-36P, UBAP2
    nsv5586634copy number variation1nstd207human GRCh38 chr9: 33,981,098-33,981,162 , GRCh37.p13 chr9: 33,981,096-33,981,160 UBAP2
    nsv5558493mobile element insertion1nstd206human GRCh38 chr9: 33,990,473-33,990,512 , GRCh37.p13 chr9: 33,990,471-33,990,510 UBAP2
    nsv5543214insertion1nstd206human GRCh38 chr9: 33,969,654-33,969,654 , GRCh37.p13 chr9: 33,969,652-33,969,652 UBAP2
    nsv5493791copy number variation1nstd206human GRCh38 chr9: 34,044,274-34,046,585 , GRCh37.p13 chr9: 34,044,272-34,046,583 UBAP2
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