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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112726copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,810,210-140,046,615 , GRCh38.p12 chr6: 133,489,072-139,725,478 SIMALR, MTFR2, 99 more genes
    nsv5905966copy number variation1nstd209human GRCh38 chr6: 138,275,785-138,275,841 , GRCh37.p13 chr6: 138,596,922-138,596,978 ARFGEF3
    nsv5903470copy number variation1nstd209human GRCh38 chr6: 138,288,345-138,289,028 , GRCh37.p13 chr6: 138,609,482-138,610,165 ARFGEF3
    nsv5903376copy number variation1nstd209human GRCh38 chr6: 138,269,426-138,270,414 , GRCh37.p13 chr6: 138,590,563-138,591,551 ARFGEF3
    nsv5902041copy number variation1nstd209human GRCh38 chr6: 138,329,441-138,331,107 , GRCh37.p13 chr6: 138,650,578-138,652,244 ARFGEF3
    nsv5901537copy number variation1nstd209human GRCh38 chr6: 138,171,024-138,171,396 , GRCh37.p13 chr6: 138,492,161-138,492,533 ARFGEF3
    nsv5893389copy number variation1nstd209human GRCh38 chr6: 137,986,656-139,086,959 , GRCh37.p13 chr6: 138,307,793-139,408,096 ECT2L, NHSL1-AS1, 17 more genes
    nsv5844044copy number variation1nstd209human GRCh38 chr6: 138,329,542-138,331,121 , GRCh37.p13 chr6: 138,650,679-138,652,258 ARFGEF3
    nsv5633999insertion1nstd207human GRCh38 chr6: 138,329,604-138,329,604 , GRCh37.p13 chr6: 138,650,741-138,650,741 ARFGEF3
    nsv5577247copy number variation1nstd207human GRCh38 chr6: 138,171,024-138,171,396 , GRCh37.p13 chr6: 138,492,161-138,492,533 ARFGEF3
    nsv5552188insertion1nstd206human GRCh38 chr6: 138,161,905-138,161,926 , GRCh37.p13 chr6: 138,483,042-138,483,063 ARFGEF3
    nsv5473199copy number variation1nstd206human GRCh38 chr6: 138,194,392-138,194,481 , GRCh37.p13 chr6: 138,515,529-138,515,618 ARFGEF3
    nsv5471130copy number variation1nstd206human GRCh38 chr6: 138,171,027-138,171,397 , GRCh37.p13 chr6: 138,492,164-138,492,534 ARFGEF3
    nsv5470936copy number variation1nstd206human GRCh38 chr6: 138,246,224-138,246,307 , GRCh37.p13 chr6: 138,567,361-138,567,444 ARFGEF3
    nsv5467911copy number variation1nstd206human GRCh38 chr6: 138,181,176-138,184,158 , GRCh37.p13 chr6: 138,502,313-138,505,295 ARFGEF3
    nsv5457171copy number variation1nstd206human GRCh38 chr6: 138,269,427-138,270,415 , GRCh37.p13 chr6: 138,590,564-138,591,552 ARFGEF3
    nsv5456877copy number variation1nstd206human GRCh38 chr6: 138,175,687-138,179,124 , GRCh37.p13 chr6: 138,496,824-138,500,261 ARFGEF3
    nsv5455506copy number variation1nstd206human GRCh38 chr6: 138,283,334-138,283,594 , GRCh37.p13 chr6: 138,604,471-138,604,731 ARFGEF3
    nsv5454548copy number variation1nstd206human GRCh38 chr6: 138,186,962-138,195,956 , GRCh37.p13 chr6: 138,508,099-138,517,093 ARFGEF3
    nsv5389108copy number variation2nstd186human GRCh37 chr6: 138,492,164-138,492,534 , GRCh38.p12 chr6: 138,171,027-138,171,397 ARFGEF3
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