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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075846inversion1nstd229human GRCh38 chr16: 84,765,092-84,765,124 , GRCh37.p13 chr16: 84,798,698-84,798,730 USP10
    nsv7073953inversion1nstd229human GRCh38 chr16: 84,385,564-84,948,716 , GRCh37.p13 chr16: 84,419,170-84,982,322 CRISPLD2, LOC123862, 10 more genes
    nsv7062698inversion1nstd229human GRCh38 chr16: 84,376,803-84,948,608 , GRCh37.p13 chr16: 84,410,409-84,982,214 LOC105371376, LINC02176, 10 more genes
    nsv6997447copy number variation1nstd229human GRCh38 chr16: 84,747,101-84,750,100 , GRCh37.p13 chr16: 84,780,707-84,783,706 USP10
    nsv6997349copy number variation1nstd229human GRCh38 chr16: 84,751,510-84,866,380 , GRCh37.p13 chr16: 84,785,116-84,899,986 USP10, CRISPLD2, 1 more genes
    nsv6992788copy number variation1nstd229human GRCh38 chr16: 84,765,170-84,765,346 , GRCh37.p13 chr16: 84,798,776-84,798,952 USP10
    nsv6991187copy number variation1nstd229human GRCh38 chr16: 84,761,101-84,764,800 , GRCh37.p13 chr16: 84,794,707-84,798,406 USP10
    nsv6988186copy number variation1nstd229human GRCh38 chr16: 84,765,972-85,486,232 , GRCh37.p13 chr16: 84,799,578-85,519,838 KIAA0513, MIR5093, 17 more genes
    nsv6988185copy number variation1nstd229human GRCh38 chr16: 84,714,966-84,732,449 , GRCh37.p13 chr16: 84,748,572-84,766,055 USP10
    nsv6985192copy number variation1nstd229human GRCh38 chr16: 84,725,849-84,996,584 , GRCh37.p13 chr16: 84,759,455-85,030,190 LOC101928474, USP10, 5 more genes
    nsv6985018copy number variation1nstd229human GRCh38 chr16: 84,777,677-84,777,738 , GRCh37.p13 chr16: 84,811,283-84,811,344 USP10
    nsv6982463copy number variation1nstd229human GRCh38 chr16: 84,703,413-84,705,483 , GRCh37.p13 chr16: 84,737,019-84,739,089 USP10
    nsv6980892copy number variation1nstd229human GRCh38 chr16: 84,714,984-84,732,457 , GRCh37.p13 chr16: 84,748,590-84,766,063 USP10
    nsv6980645copy number variation1nstd229human GRCh38 chr16: 84,719,070-84,722,835 , GRCh37.p13 chr16: 84,752,676-84,756,441 USP10
    nsv6980319copy number variation1nstd229human GRCh38 chr16: 84,592,847-85,544,248 , GRCh37.p13 chr16: 84,626,453-85,577,854 COX6CP16, LINC02176, 20 more genes
    nsv6980309copy number variation1nstd229human GRCh38 chr16: 84,702,757-84,707,844 , GRCh37.p13 chr16: 84,736,363-84,741,450 USP10
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6623939copy number variation1nstd224human GRCh37 chr16: 84,576,287-84,947,677 , GRCh38.p12 chr16: 84,542,681-84,914,071 USP10, COTL1, 5 more genes
    nsv6595280inversion1nstd223human GRCh38 chr16: 84,771,710-84,772,147 , GRCh37.p13 chr16: 84,805,316-84,805,753 USP10
    nsv6592180inversion1nstd223human GRCh38 chr16: 84,702,263-84,702,910 , GRCh37.p13 chr16: 84,735,869-84,736,516 USP10
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