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Items: 1 to 20 of 277

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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
    nsv7142585insertion1nstd232human GRCh37.p13 chr3: 119,419,919-119,419,919 , GRCh38.p12 chr3: 119,701,072-119,701,072 CFAP91, LOC105374064
    nsv7043452inversion1nstd229human GRCh38 chr3: 119,694,898-119,720,795 , GRCh37.p13 chr3: 119,413,745-119,439,642 CFAP91, LOC105374064
    nsv7041333inversion1nstd229human GRCh38 chr3: 119,602,733-121,708,334 , GRCh37.p13 chr3: 119,321,580-121,427,181 RABL3, PTOV1P1, 44 more genes
    nsv7039920inversion1nstd229human GRCh38 chr3: 119,602,735-121,711,940 , GRCh37.p13 chr3: 119,321,582-121,430,787 LINC02049, GSK3B, 44 more genes
    nsv6713409copy number variation1nstd229human GRCh38 chr3: 119,707,001-119,745,100 , GRCh37.p13 chr3: 119,425,848-119,463,947 CFAP91
    nsv6712539copy number variation1nstd229human GRCh38 chr3: 119,766,435-119,767,144 , GRCh37.p13 chr3: 119,485,282-119,485,991 CFAP91
    nsv6707973copy number variation1nstd229human GRCh38 chr3: 119,717,903-119,717,943 , GRCh37.p13 chr3: 119,436,750-119,436,790 CFAP91
    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
    nsv6704191copy number variation1nstd229human GRCh38 chr3: 119,722,771-119,722,846 , GRCh37.p13 chr3: 119,441,618-119,441,693 CFAP91
    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
    nsv6702306copy number variation1nstd229human GRCh38 chr3: 119,719,888-119,722,380 , GRCh37.p13 chr3: 119,438,735-119,441,227 CFAP91
    nsv6698757copy number variation1nstd229human GRCh38 chr3: 119,741,349-119,741,734 , GRCh37.p13 chr3: 119,460,196-119,460,581 CFAP91
    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
    nsv6574329inversion1nstd223human GRCh38 chr3: 119,712,961-119,713,262 , GRCh37.p13 chr3: 119,431,808-119,432,109 CFAP91
    nsv6566301inversion1nstd223human GRCh38 chr3: 119,712,689-119,713,268 , GRCh37.p13 chr3: 119,431,536-119,432,115 CFAP91
    nsv6563134inversion1nstd223human GRCh38 chr3: 119,730,757-119,730,913 , GRCh37.p13 chr3: 119,449,604-119,449,760 CFAP91
    nsv6558695inversion1nstd223human GRCh38 chr3: 115,305,653-119,971,699 , GRCh37.p13 chr3: 115,024,500-119,690,546 LOC105374060, RN7SL815P, 52 more genes
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