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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097266copy number variation1nstd102humanPathogenic GRCh37 chr5: 167,849,013-169,661,202 , GRCh38.p12 chr5: 168,422,008-170,234,198 FBLL1, RNU6-477P, 25 more genes
    nsv7048806inversion1nstd229human GRCh38 chr5: 168,414,285-168,784,754 , GRCh37.p13 chr5: 167,841,290-168,211,759 FBLL1, MIR103A1, 9 more genes
    nsv7045785inversion1nstd229human GRCh38 chr5: 168,435,446-168,441,035 , GRCh37.p13 chr5: 167,862,451-167,868,040 WWC1
    nsv7042332inversion1nstd229human GRCh38 chr5: 168,444,570-168,573,004 , GRCh37.p13 chr5: 167,871,575-168,000,009 WWC1, FBLL1, 5 more genes
    nsv7042003inversion1nstd229human GRCh38 chr5: 168,420,309-168,420,422 , GRCh37.p13 chr5: 167,847,314-167,847,427 WWC1
    nsv7041097inversion1nstd229human GRCh38 chr5: 168,349,109-168,349,162 , GRCh37.p13 chr5: 167,776,114-167,776,167 WWC1
    nsv7039401inversion1nstd229human GRCh38 chr5: 168,394,338-168,414,732 , GRCh37.p13 chr5: 167,821,343-167,841,737 WWC1
    nsv6797479copy number variation1nstd229human GRCh38 chr5: 168,359,831-168,360,043 , GRCh37.p13 chr5: 167,786,836-167,787,048 WWC1
    nsv6795890copy number variation1nstd229human GRCh38 chr5: 168,418,854-168,419,241 , GRCh37.p13 chr5: 167,845,859-167,846,246 WWC1
    nsv6795876copy number variation1nstd229human GRCh38 chr5: 168,346,346-168,352,869 , GRCh37.p13 chr5: 167,773,351-167,779,874 WWC1
    nsv6793913copy number variation1nstd229human GRCh38 chr5: 168,432,353-168,558,092 , GRCh37.p13 chr5: 167,859,358-167,985,097 SLC2A3P1, WWC1, 3 more genes
    nsv6791960copy number variation1nstd229human GRCh38 chr5: 168,348,765-168,355,225 , GRCh37.p13 chr5: 167,775,770-167,782,230 WWC1
    nsv6788616copy number variation1nstd229human GRCh38 chr5: 168,351,107-168,357,588 , GRCh37.p13 chr5: 167,778,112-167,784,593 WWC1
    nsv6787512copy number variation1nstd229human GRCh38 chr5: 168,444,901-168,451,900 , GRCh37.p13 chr5: 167,871,906-167,878,905 WWC1
    nsv6786346copy number variation1nstd229human GRCh38 chr5: 168,469,611-168,480,630 , GRCh37.p13 chr5: 167,896,616-167,907,635 WWC1
    nsv6786083copy number variation1nstd229human GRCh38 chr5: 168,400,006-168,404,667 , GRCh37.p13 chr5: 167,827,011-167,831,672 WWC1
    nsv6785923copy number variation1nstd229human GRCh38 chr5: 168,465,189-168,465,259 , GRCh37.p13 chr5: 167,892,194-167,892,264 WWC1
    nsv6785722copy number variation1nstd229human GRCh38 chr5: 168,368,073-168,377,398 , GRCh37.p13 chr5: 167,795,078-167,804,403 WWC1
    nsv6783763copy number variation1nstd229human GRCh38 chr5: 168,309,244-168,309,330 , GRCh37.p13 chr5: 167,736,249-167,736,335 WWC1
    nsv6783543copy number variation1nstd229human GRCh38 chr5: 168,394,301-168,784,700 , GRCh37.p13 chr5: 167,821,306-168,211,705 RPL10P9, WWC1, 9 more genes
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