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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098719copy number variation1nstd102humanUncertain significance GRCh38 chr5: 63,960,681-63,960,740 , GRCh37 chr5: 63,256,508-63,256,567 HTR1A
    nsv7046562inversion1nstd229human GRCh38 chr5: 63,953,105-63,957,288 , GRCh37.p13 chr5: 63,248,932-63,253,115 HTR1A
    nsv6776236copy number variation1nstd229human GRCh38 chr5: 63,822,048-64,455,445 , GRCh37.p13 chr5: 63,117,875-63,751,272 HTR1A, RNF180, 1 more genes
    nsv6762960copy number variation1nstd229human GRCh38 chr5: 63,951,501-63,964,900 , GRCh37.p13 chr5: 63,247,328-63,260,727 HTR1A
    nsv6758689copy number variation1nstd229human GRCh38 chr5: 63,231,578-64,664,500 , GRCh37.p13 chr5: 62,527,405-63,960,327 RNF180, RN7SL169P, 6 more genes
    nsv6630784copy number variation1nstd224human GRCh37 chr5: 63,250,851-63,404,744 , GRCh38.p12 chr5: 63,955,024-64,108,917 HTR1A
    nsv6315417copy number variation1nstd102humanPathogenic GRCh37 chr5: 59,783,655-63,257,950 , GRCh38.p12 chr5: 60,487,828-63,962,123 ERCC8, SMIM15-AS1, 41 more genes
    nsv6312114copy number variation1nstd102humanPathogenic GRCh37 chr5: 63,256,278-65,374,358 , GRCh38.p12 chr5: 63,960,451-66,078,530 RNF180, RPEP1, 23 more genes
    nsv6136128copy number variation1nstd213human GRCh37 chr5: 62,820,000-66,080,001 , GRCh38.p12 chr5: 63,524,173-66,784,173 TRIM23, HTR1A, 33 more genes
    nsv6135679copy number variation1nstd213human GRCh37 chr5: 62,820,000-63,330,001 , GRCh38.p12 chr5: 63,524,173-64,034,174 HTR1A, LOC105378999, 1 more genes
    nsv6135416copy number variation1nstd213human GRCh37 chr5: 50,510,000-68,870,001 , GRCh38.p12 chr5: 51,214,166-69,574,174 , TRIM23, 243 more genes
    nsv6135191copy number variation1nstd213human GRCh37 chr5: 63,120,000-63,300,001 , GRCh38.p12 chr5: 63,824,173-64,004,174 HTR1A, LOC105378999
    nsv4591494copy number variation1nstd183human GRCh37 chr5: 63,118,266-63,748,718 , GRCh38.p12 chr5: 63,822,439-64,452,891 RNF180, HTR1A, 1 more genes
    nsv4578696copy number variation1nstd102humanLikely pathogenic GRCh38 chr5: 58,780,641-73,523,380 , GRCh37.p13 chr5: 58,076,468-72,819,205 TRIM23, BTF3, 215 more genes
    nsv4521974copy number variation1nstd166human GRCh37.p13 chr5: 62,877,999-63,488,200 , GRCh38.p12 chr5: 63,582,172-64,192,373 LOC107986416, RNF180, 2 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4337631sequence alteration1nstd166human GRCh37.p13 chr5: 59,960,463-64,048,177 , GRCh38.p12 chr5: 60,664,636-64,752,350 , ERCC8, 46 more genes
    nsv4131633copy number variation1nstd166human GRCh37.p13 chr5: 62,527,405-63,960,327 , GRCh38.p12 chr5: 63,231,578-64,664,500 , HTR1A, 7 more genes
    nsv4119813copy number variation1nstd166human GRCh37.p13 chr5: 39,131,458-67,637,618 , GRCh38.p12 chr5: 39,131,356-68,341,790 , ESM1, 305 more genes
    nsv3920421copy number variation1nstd102humanLikely pathogenic NCBI36 chr5: 62,538,695-70,622,774 , GRCh37 chr5: 62,502,939-70,587,018 , GRCh38 chr5: 63,207,112-71,291,191 TRIM23, CCNB1, 124 more genes
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