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Items: 1 to 20 of 265

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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
    nsv7096531copy number variation1nstd102humanUncertain significance GRCh37 chr3: 121,489,192-125,313,644 , GRCh38.p12 chr3: 121,770,345-125,594,800 MEMO1P6, HACD2, 62 more genes
    nsv7051864inversion1nstd229human GRCh38 chr3: 121,708,189-122,055,779 , GRCh37.p13 chr3: 121,427,036-121,774,626 GOLGB1, LOC101927010, 5 more genes
    nsv7051687inversion1nstd229human GRCh38 chr3: 121,633,562-121,844,144 , GRCh37.p13 chr3: 121,352,409-121,562,991 GOLGB1, IQCB1, 4 more genes
    nsv7046540inversion1nstd229human GRCh38 chr3: 121,879,351-122,055,789 , GRCh37.p13 chr3: 121,598,198-121,774,636 LOC101927010, CD86, 3 more genes
    nsv6717236copy number variation1nstd229human GRCh38 chr3: 121,868,002-121,873,471 , GRCh37.p13 chr3: 121,586,849-121,592,318 EAF2
    nsv6710031copy number variation1nstd229human GRCh38 chr3: 121,845,461-121,854,335 , GRCh37.p13 chr3: 121,564,308-121,573,182 EAF2
    nsv6708326copy number variation1nstd229human GRCh38 chr3: 121,664,201-121,844,100 , GRCh37.p13 chr3: 121,383,048-121,562,947 GOLGB1, IQCB1, 1 more genes
    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
    nsv6706228copy number variation1nstd229human GRCh38 chr3: 121,126,833-121,857,712 , GRCh37.p13 chr3: 120,845,680-121,576,559 POLQ, GOLGB1, 10 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
    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
    nsv6569581inversion1nstd223human GRCh38 chr3: 121,192,997-121,858,688 , GRCh37.p13 chr3: 120,911,844-121,577,535 RPL7AP11, STXBP5L, 10 more genes
    nsv6567732inversion1nstd223human GRCh38 chr3: 121,881,709-121,882,074 , GRCh37.p13 chr3: 121,600,556-121,600,921 EAF2
    nsv6565554inversion1nstd223human GRCh38 chr3: 121,884,066-121,884,476 , GRCh37.p13 chr3: 121,602,913-121,603,323 EAF2
    nsv6562801inversion1nstd223human GRCh38 chr3: 121,881,818-121,882,335 , GRCh37.p13 chr3: 121,600,665-121,601,182 EAF2
    nsv6371782copy number variation1nstd223human GRCh38 chr3: 121,848,423-121,848,941 , GRCh37.p13 chr3: 121,567,270-121,567,788 EAF2
    nsv6368765copy number variation1nstd223human GRCh38 chr3: 121,872,292-121,872,982 , GRCh37.p13 chr3: 121,591,139-121,591,829 EAF2
    nsv6311770copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,365,818-133,465,047 , GRCh38.p12 chr3: 120,646,971-133,746,203 HNRNPA1P23, MIX23, 278 more genes
    nsv6254612mobile element insertion1nstd215human GRCh38 chr3: 121,849,972-121,849,972 , GRCh37.p13 chr3: 121,568,819-121,568,819 EAF2
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