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Items: 1 to 20 of 192

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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
    nsv7049104inversion1nstd229human GRCh38 chr3: 114,751,914-119,661,867 , GRCh37.p13 chr3: 114,470,761-119,380,714 LINC00901, EIF4E2P2, 50 more genes
    nsv6712012copy number variation1nstd229human GRCh38 chr3: 119,514,501-119,523,200 , GRCh37.p13 chr3: 119,233,348-119,242,047 TIMMDC1, CD80
    nsv6709115copy number variation1nstd229human GRCh38 chr3: 119,514,257-119,515,133 , GRCh37.p13 chr3: 119,233,104-119,233,980 TIMMDC1
    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
    nsv6704409copy number variation1nstd229human GRCh38 chr3: 119,468,099-119,806,079 , GRCh37.p13 chr3: 119,186,946-119,524,926 POPDC2, CFAP91, 13 more genes
    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
    nsv6702544copy number variation1nstd229human GRCh38 chr3: 119,505,897-119,509,074 , GRCh37.p13 chr3: 119,224,744-119,227,921 TIMMDC1
    nsv6699554copy number variation1nstd229human GRCh38 chr3: 119,510,712-119,573,194 , GRCh37.p13 chr3: 119,229,559-119,292,041 CSRP2P1, TIMMDC1, 2 more genes
    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
    nsv6573730inversion1nstd223human GRCh38 chr3: 119,512,652-119,514,949 , GRCh37.p13 chr3: 119,231,499-119,233,796 TIMMDC1
    nsv6565807inversion1nstd223human GRCh38 chr3: 119,509,089-119,509,694 , GRCh37.p13 chr3: 119,227,936-119,228,541 TIMMDC1
    nsv6564002inversion1nstd223human GRCh38 chr3: 119,504,938-119,505,661 , GRCh37.p13 chr3: 119,223,785-119,224,508 TIMMDC1
    nsv6559467inversion1nstd223human GRCh38 chr3: 119,509,042-119,509,530 , GRCh37.p13 chr3: 119,227,889-119,228,377 TIMMDC1
    nsv6558695inversion1nstd223human GRCh38 chr3: 115,305,653-119,971,699 , GRCh37.p13 chr3: 115,024,500-119,690,546 LOC105374060, RN7SL815P, 52 more genes
    nsv6357445copy number variation1nstd223human GRCh38 chr3: 119,514,234-119,515,109 , GRCh37.p13 chr3: 119,233,081-119,233,956 TIMMDC1
    nsv6134575copy number variation1nstd213human GRCh37 chr3: 116,870,000-132,100,001 , GRCh38.p12 chr3: 117,151,153-132,381,157 ACP3, ADCY5, 308 more genes
    nsv5991082copy number variation1nstd212human GRCh38 chr3: 119,501,505-119,501,934 , GRCh37.p13 chr3: 119,220,352-119,220,781 TIMMDC1
    nsv5893813copy number variation1nstd209human GRCh38 chr3: 119,514,234-119,515,108 , GRCh37.p13 chr3: 119,233,081-119,233,955 TIMMDC1
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