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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv3921568copy number variation1nstd102humanPathogenic GRCh37 chr5: 64,228,590-68,791,331 , NCBI36 chr5: 64,264,346-68,827,087 , GRCh38 chr5: 64,932,763-69,495,504 LOC100419549, MAST4-AS1, 67 more genes
    nsv3920547copy number variation1nstd102humanUncertain significance GRCh38 chr5: 65,976,124-71,317,474 , NCBI36 chr5: 65,307,708-70,649,057 , GRCh37 chr5: 65,271,952-70,613,301 SMN1, NAIP, 97 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
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
    nsv3911585copy number variation1nstd102humanPathogenic NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550 LINC02241, ATPSCKMT, 878 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 MEGF10, LOC100128407, 2080 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 LOC105374618, HARS1, 2499 more genes
    nsv3883692copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 58,966,132-68,847,066 , GRCh38.p12 chr5: 59,670,306-69,551,239 TRIM23, CCNB1, 125 more genes
    nsv3875235copy number variation2nstd102humanPathogenic GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788 SPEF2, NDST1, 2490 more genes
    nsv3875076copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 65,315,606-68,755,816 , GRCh38.p12 chr5: 66,019,778-69,459,989 CCNB1, CDK7, 47 more genes
    nsv3871533copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343 PCDHGC5, RGS14, 2492 more genes
    nsv2340665short tandem repeat3nstd128human GRCh37 chr5: 68,150,383-68,150,419 , GRCh38.p12 chr5: 68,854,556-68,854,592 VWA8P1
    nsv1151912copy number variation1nstd107human GRCh37 chr5: 1,853,522-70,970,788 , GRCh38.p12 chr5: 1,853,408-71,674,961 , ASS1P9, 808 more genes
    nsv1142631copy number variation1nstd106human GRCh37 chr5: 22,170,166-70,699,299 , GRCh38.p12 chr5: 22,170,057-71,403,472 , LINC02108, 571 more genes
    esv3815459copy number variation1estd192human GRCh37 chr5: 55,448,215-119,510,134 , GRCh38.p12 chr5: 56,152,388-120,174,439 , LOC105379138, 829 more genes
    esv3803325copy number variation1estd192human GRCh37 chr5: 55,814,376-95,636,328 , GRCh38.p12 chr5: 56,518,549-96,300,624 , LOC100130001, 560 more genes
    esv3805596copy number variation1estd192human GRCh37 chr5: 60,947,413-72,070,572 , GRCh38.p12 chr5: 61,651,586-72,774,745 , MRPS27, 179 more genes
    esv3803260tandem duplication2estd192human GRCh37 chr5: 41,392,808-111,332,151 , GRCh38.p12 chr5: 41,392,706-111,996,454 , LINC02118, 865 more genes
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