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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144715insertion1nstd232human GRCh37.p13 chr5: 140,862,322-140,862,322 , GRCh38.p12 chr5: 141,482,755-141,482,755 PCDHGB3, PCDHGA11, 19 more genes
    nsv7057082inversion1nstd229human GRCh38 chr5: 139,208,712-142,493,851 , GRCh37.p13 chr5: 138,544,401-141,873,416 SPRY4-AS1, SPRY4, 151 more genes
    nsv7055264inversion1nstd229human GRCh38 chr5: 141,397,100-141,397,151 , GRCh37.p13 chr5: 140,776,667-140,776,718 PCDHGB5, PCDHGB1, 12 more genes
    nsv6795088copy number variation1nstd229human GRCh38 chr5: 141,480,314-141,482,754 , GRCh37.p13 chr5: 140,859,881-140,862,321 PCDHGA8, PCDHGA1, 19 more genes
    nsv6793509copy number variation1nstd229human GRCh38 chr5: 141,510,901-141,517,000 , GRCh37.p13 chr5: 140,890,468-140,896,567 PCDHGA1, PCDHGA7, 22 more genes
    nsv6790325copy number variation1nstd229human GRCh38 chr5: 141,511,568-141,511,774 , GRCh37.p13 chr5: 140,891,135-140,891,341 PCDHGB6, PCDHGB2, 21 more genes
    nsv6788179copy number variation1nstd229human GRCh38 chr5: 141,421,704-141,425,746 , GRCh37.p13 chr5: 140,801,271-140,805,313 PCDHGB4, PCDHG@, 18 more genes
    nsv6786654copy number variation1nstd229human GRCh38 chr5: 141,430,970-141,436,047 , GRCh37.p13 chr5: 140,810,537-140,815,614 PCDHGA1, PCDHGA8, 18 more genes
    nsv6786281copy number variation1nstd229human GRCh38 chr5: 141,505,481-141,510,945 , GRCh37.p13 chr5: 140,885,048-140,890,512 PCDHGA11, PCDHGB3, 21 more genes
    nsv6785934copy number variation1nstd229human GRCh38 chr5: 141,174,601-142,728,000 , GRCh37.p13 chr5: 140,687,717-142,107,565 TAF7, RNF14, 64 more genes
    nsv6785857copy number variation1nstd229human GRCh38 chr5: 141,495,087-141,497,917 , GRCh37.p13 chr5: 140,874,654-140,877,484 PCDHGA10, PCDHGC4, 21 more genes
    nsv6778548copy number variation1nstd229human GRCh38 chr5: 141,387,501-141,398,200 , GRCh37.p13 chr5: 140,767,068-140,777,767 PCDHGB1, PCDHGA4, 12 more genes
    nsv6778130copy number variation1nstd229human GRCh38 chr5: 141,485,723-141,486,291 , GRCh37.p13 chr5: 140,865,290-140,865,858 PCDHGA9, PCDHGA2, 20 more genes
    nsv6636181copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 140,865,418-140,865,497 , GRCh38 chr5: 141,485,851-141,485,930 PCDHGC3, PCDHGB4, 20 more genes
    nsv6572268inversion1nstd223human GRCh38 chr5: 141,456,104-141,456,705 , GRCh37.p13 chr5: 140,835,671-140,836,272 PCDHGB2, PCDHGB6, 18 more genes
    nsv6560252inversion1nstd223human GRCh38 chr5: 141,449,596-141,450,315 , GRCh37.p13 chr5: 140,829,163-140,829,882 PCDHGB7, PCDHGB3, 18 more genes
    nsv6559545inversion1nstd223human GRCh38 chr5: 141,447,149-141,448,154 , GRCh37.p13 chr5: 140,826,716-140,827,721 PCDHGA4, PCDHGA7, 18 more genes
    nsv6558167inversion1nstd223human GRCh38 chr5: 141,463,475-141,463,995 , GRCh37.p13 chr5: 140,843,042-140,843,562 PCDHGB5, PCDHGA12, 18 more genes
    nsv6413195copy number variation1nstd223human GRCh38 chr5: 141,404,125-141,404,658 , GRCh37.p13 chr5: 140,783,692-140,784,225 PCDHGA6, PCDHGA3, 13 more genes
    nsv6412644copy number variation1nstd223human GRCh38 chr5: 141,415,067-141,423,035 , GRCh37.p13 chr5: 140,794,634-140,802,602 PCDHGA3, PCDHG@, 17 more genes
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