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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
    nsv7057161inversion1nstd229human GRCh38 chr5: 141,377,317-141,379,850 , GRCh37.p13 chr5: 140,756,884-140,759,417 PCDHGB1, PCDHGA5, 8 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
    nsv7055899inversion1nstd229human GRCh38 chr5: 141,375,483-141,377,554 , GRCh37.p13 chr5: 140,755,050-140,757,121 PCDHGA1, PCDHGA4, 8 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
    nsv6797907copy number variation1nstd229human GRCh38 chr5: 141,378,268-141,382,142 , GRCh37.p13 chr5: 140,757,835-140,761,709 PCDHGB2, PCDHGA4, 9 more genes
    nsv6797620copy number variation1nstd229human GRCh38 chr5: 141,367,003-141,367,037 , GRCh37.p13 chr5: 140,746,570-140,746,604 PCDHGB1, PCDHGA5, 6 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
    nsv6636350copy number variation1nstd102humanUncertain significance GRCh37 chr5: 140,082,762-140,773,954 , GRCh38.p12 chr5: 140,703,177-141,394,387 PCDHA13, PCDHA10, 61 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
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