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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094183copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,421-75,283,128 , GRCh38.p12 chr11: 71,435,375-75,572,083 LOC112268078, LRTOMT, 142 more genes
    nsv6908275copy number variation1nstd229human GRCh38 chr11: 71,281,500-72,194,614 , GRCh37.p13 chr11: 71,088,949-71,905,658 DEFB130C, ANAPC15, 40 more genes
    nsv6898152copy number variation1nstd229human GRCh38 chr11: 72,135,925-72,135,961 , GRCh37.p13 chr11: 71,846,971-71,847,007 FOLR3
    nsv6637545copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,777,538-72,144,933 , GRCh38.p12 chr11: 72,066,492-72,433,889 CLPB, FOLR3, 15 more genes
    nsv6577125inversion1nstd223human GRCh38 chr11: 72,137,499-72,138,245 , GRCh37.p13 chr11: 71,848,545-71,849,291 FOLR3
    nsv6470560copy number variation1nstd223human GRCh38 chr11: 72,025,209-72,302,197 , GRCh37.p13 chr11: 71,736,255-72,013,241 CLPB, FOLR3, 14 more genes
    nsv6468780copy number variation1nstd223human GRCh38 chr11: 72,136,048-72,172,507 , GRCh37.p13 chr11: 71,847,094-71,883,551 FOLR3P1, FOLR1P1, 1 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6314007copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,567,724-72,488,649 , GRCh38.p12 chr11: 71,856,678-72,777,604 STARD10, PDE2A, 38 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5355353translocation1nstd200human GRCh38 chr11: 72,139,219-72,139,219 , GRCh38 chr11: 72,177,195-72,177,195 , GRCh37.p13 chr11: 71,850,263-71,850,263 , GRCh37.p13 chr11: 71,888,239-71,888,239 FOLR3, FOLR3P1
    nsv5331481translocation1nstd200human GRCh37 chr11: 71,850,263-71,850,263 , GRCh37 chr11: 71,888,239-71,888,239 , GRCh38.p12 chr11: 72,139,219-72,139,219 , GRCh38.p12 chr11: 72,177,195-72,177,195 FOLR3, FOLR3P1
    nsv5278677copy number variation1nstd204human GRCh37.p13 chr11: 71,772,747-71,889,344 , GRCh38.p13 chr11: 72,061,701-72,178,300 FOLR3, NUMA1, 7 more genes
    nsv4985128copy number variation1nstd200human GRCh38 chr11: 72,135,955-72,172,560 , GRCh37.p13 chr11: 71,847,001-71,883,604 FOLR1P1, FOLR3P1, 1 more genes
    nsv4681893copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,401-71,907,241 , GRCh38.p12 chr11: 71,435,355-72,196,197 OR7E128P, ZNF705EP, 39 more genes
    nsv4425434copy number variation1nstd174human GRCh37 chr11: 71,847,797-71,890,984 , GRCh38.p12 chr11: 72,136,751-72,179,940 FOLR1P1, FOLR3, 1 more genes
    nsv4415121copy number variation1nstd174human GRCh37 chr11: 71,846,443-71,892,793 , GRCh38.p12 chr11: 72,135,397-72,181,749 FOLR3, FOLR1P1, 1 more genes
    nsv4376986copy number variation1nstd173human GRCh37 chr11: 71,847,808-71,873,232 , GRCh38.p12 chr11: 72,136,762-72,162,188 FOLR1P1, FOLR3
    nsv4372237copy number variation2nstd173human GRCh37 chr11: 71,847,228-71,873,232 , GRCh38.p12 chr11: 72,136,182-72,162,188 FOLR3, FOLR1P1
    nsv4205732copy number variation1nstd166human GRCh37.p13 chr11: 71,848,500-71,886,000 , GRCh38.p12 chr11: 72,137,454-72,174,956 FOLR3P1, FOLR3, 1 more genes
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