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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7057420inversion1nstd229human GRCh38 chr3: 119,176,856-119,176,913 , GRCh37.p13 chr3: 118,895,703-118,895,760 UPK1B
    nsv7051881inversion1nstd229human GRCh38 chr3: 119,069,449-119,472,399 , GRCh37.p13 chr3: 118,788,296-119,191,246 B4GALT4, RNU6-1127P, 9 more genes
    nsv7049698inversion1nstd229human GRCh38 chr3: 119,187,204-119,198,240 , GRCh37.p13 chr3: 118,906,051-118,917,087 UPK1B
    nsv7049104inversion1nstd229human GRCh38 chr3: 114,751,914-119,661,867 , GRCh37.p13 chr3: 114,470,761-119,380,714 LINC00901, EIF4E2P2, 50 more genes
    nsv6714040copy number variation1nstd229human GRCh38 chr3: 119,135,323-119,250,941 , GRCh37.p13 chr3: 118,854,170-118,969,788 TEX55, B4GALT4-AS1, 3 more genes
    nsv6713840copy number variation1nstd229human GRCh38 chr3: 119,121,101-119,191,700 , GRCh37.p13 chr3: 118,839,948-118,910,547 IGSF11, TEX55, 1 more genes
    nsv6712660copy number variation1nstd229human GRCh38 chr3: 119,178,701-119,183,700 , GRCh37.p13 chr3: 118,897,548-118,902,547 UPK1B
    nsv6709379copy number variation1nstd229human GRCh38 chr3: 119,182,224-119,192,640 , GRCh37.p13 chr3: 118,901,071-118,911,487 UPK1B
    nsv6707907copy number variation1nstd229human GRCh38 chr3: 113,856,250-122,791,940 , GRCh37.p13 chr3: 113,575,097-122,510,787 COX17, LOC105374052, 133 more genes
    nsv6707813copy number variation1nstd229human GRCh38 chr3: 119,177,258-119,179,580 , GRCh37.p13 chr3: 118,896,105-118,898,427 UPK1B
    nsv6703931copy number variation1nstd229human GRCh38 chr3: 118,573,267-126,079,281 , GRCh37.p13 chr3: 118,292,114-125,798,124 RPS24P9, LOC105374064, 149 more genes
    nsv6702830copy number variation1nstd229human GRCh38 chr3: 119,187,201-119,206,200 , GRCh37.p13 chr3: 118,906,048-118,925,047 UPK1B
    nsv6701887copy number variation1nstd229human GRCh38 chr3: 119,136,526-119,283,876 , GRCh37.p13 chr3: 118,855,373-119,002,723 B4GALT4-AS1, B4GALT4, 3 more genes
    nsv6701524copy number variation1nstd229human GRCh38 chr3: 119,172,801-119,184,300 , GRCh37.p13 chr3: 118,891,648-118,903,147 UPK1B
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6637150copy number variation1nstd102humanUncertain significance GRCh37 chr3: 116,109,191-120,328,013 , GRCh38.p12 chr3: 116,390,344-120,609,166 LOC101926953, LOC105374058, 60 more genes
    nsv6558695inversion1nstd223human GRCh38 chr3: 115,305,653-119,971,699 , GRCh37.p13 chr3: 115,024,500-119,690,546 LOC105374060, RN7SL815P, 52 more genes
    nsv6373713copy number variation1nstd223human GRCh38 chr3: 119,178,701-119,183,600 , GRCh37.p13 chr3: 118,897,548-118,902,447 UPK1B
    nsv6372571copy number variation1nstd223human GRCh38 chr3: 119,196,646-119,206,078 , GRCh37.p13 chr3: 118,915,493-118,924,925 UPK1B
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