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Items: 1 to 20 of 147

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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
    nsv7076680inversion1nstd229human GRCh38 chr11: 72,466,691-73,774,399 , GRCh37.p13 chr11: 72,177,735-73,485,444 OR8R1P, PDE2A, 33 more genes
    nsv7075390inversion1nstd229human GRCh38 chr11: 72,466,687-73,774,399 , GRCh37.p13 chr11: 72,177,731-73,485,444 RAB6A, MIR139, 33 more genes
    nsv7069623inversion1nstd229human GRCh38 chr11: 73,257,626-73,338,349 , GRCh37.p13 chr11: 72,968,671-73,049,394 LOC105369382, P2RY6, 2 more genes
    nsv6910780copy number variation1nstd229human GRCh38 chr11: 73,227,625-73,480,382 , GRCh37.p13 chr11: 72,938,670-73,191,427 ARHGEF17-AS1, FAM168A, 6 more genes
    nsv6908862copy number variation1nstd229human GRCh38 chr11: 73,268,567-73,270,804 , GRCh37.p13 chr11: 72,979,612-72,981,849 P2RY6
    nsv6908633copy number variation1nstd229human GRCh38 chr11: 73,291,218-73,297,119 , GRCh37.p13 chr11: 73,002,263-73,008,164 P2RY6
    nsv6904187copy number variation1nstd229human GRCh38 chr11: 73,250,563-73,307,540 , GRCh37.p13 chr11: 72,961,608-73,018,585 ARHGEF17, ARHGEF17-AS1, 2 more genes
    nsv6901405copy number variation1nstd229human GRCh38 chr11: 73,289,408-73,291,761 , GRCh37.p13 chr11: 73,000,453-73,002,806 P2RY6
    nsv6898622copy number variation1nstd229human GRCh38 chr11: 73,272,666-73,273,085 , GRCh37.p13 chr11: 72,983,711-72,984,130 P2RY6
    nsv6457085copy number variation1nstd223human GRCh38 chr11: 73,289,270-73,291,723 , GRCh37.p13 chr11: 73,000,315-73,002,768 P2RY6
    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
    nsv5913360copy number variation1nstd209human GRCh38 chr11: 73,289,408-73,291,760 , GRCh37.p13 chr11: 73,000,453-73,002,805 P2RY6
    nsv5866843copy number variation1nstd209human GRCh38 chr11: 73,289,380-73,291,522 , GRCh37.p13 chr11: 73,000,425-73,002,567 P2RY6
    nsv5506591copy number variation1nstd206human GRCh38 chr11: 73,289,388-73,291,787 , GRCh37.p13 chr11: 73,000,433-73,002,832 P2RY6
    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
    nsv5339419translocation1nstd200human GRCh37 chr11: 73,010,007-73,010,007 , GRCh37 chr11: 73,009,860-73,009,860 , GRCh38.p12 chr11: 73,298,815-73,298,815 , GRCh38.p12 chr11: 73,298,962-73,298,962 P2RY6
    nsv5301435copy number variation1nstd204human GRCh38.p13 chr11: 73,298,789-73,298,987 , GRCh37.p13 chr11: 73,009,834-73,010,032 P2RY6
    nsv5271506copy number variation1nstd204human GRCh38.p13 chr11: 73,251,201-73,280,600 , GRCh37.p13 chr11: 72,962,246-72,991,645 P2RY6, LOC105369382
    nsv5128799mobile element insertion1nstd203human GRCh38 chr11: 73,274,496-73,274,540 , GRCh37.p13 chr11: 72,985,541-72,985,585 P2RY6
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