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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
    nsv7074999inversion1nstd229human GRCh38 chr11: 82,855,180-83,018,680 , GRCh37.p13 chr11: 82,566,222-82,729,722 RAB30, DDIAS, 2 more genes
    nsv7062836inversion1nstd229human GRCh38 chr11: 82,851,177-83,079,109 , GRCh37.p13 chr11: 82,562,219-82,790,151 PRCP, RAB30-DT, 4 more genes
    nsv6916297copy number variation1nstd229human GRCh38 chr11: 82,904,701-82,961,800 , GRCh37.p13 chr11: 82,615,743-82,672,842 DDIAS, RPL7AP54
    nsv6913950copy number variation1nstd229human GRCh38 chr11: 82,875,883-82,995,968 , GRCh37.p13 chr11: 82,586,925-82,707,010 DDIAS, PRCP, 2 more genes
    nsv6908348copy number variation1nstd229human GRCh38 chr11: 82,906,725-82,907,050 , GRCh37.p13 chr11: 82,617,767-82,618,092 DDIAS
    nsv6637847copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,562,738-88,663,067 , GRCh38.p12 chr11: 80,851,695-88,929,899 PRSS23, MTCO3P25, 92 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6469718copy number variation1nstd223human GRCh38 chr11: 82,915,203-82,915,939 , GRCh37.p13 chr11: 82,626,245-82,626,981 DDIAS
    nsv6465150copy number variation1nstd223human GRCh38 chr11: 82,899,901-82,902,400 , GRCh37.p13 chr11: 82,610,943-82,613,442 DDIAS, PRCP
    nsv6463351copy number variation1nstd223human GRCh38 chr11: 82,908,332-82,920,423 , GRCh37.p13 chr11: 82,619,374-82,631,465 DDIAS
    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
    nsv6313961copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,855,209-98,002,445 , GRCh38.p12 chr11: 78,144,163-98,131,717 MTND5P38, XIAPP2, 252 more genes
    nsv6132383copy number variation1nstd213human GRCh37 chr11: 82,220,000-82,730,001 , GRCh38.p12 chr11: 82,508,958-83,018,959 PRCP, RAB30, 7 more genes
    nsv5926661copy number variation1nstd209human GRCh38 chr11: 82,906,652-82,907,122 , GRCh37.p13 chr11: 82,617,694-82,618,164 DDIAS
    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
    nsv5361508translocation1nstd200human GRCh38 chr11: 82,907,123-82,907,123 , GRCh38 chr11: 82,906,652-82,906,652 , GRCh37.p13 chr11: 82,617,694-82,617,694 , GRCh37.p13 chr11: 82,618,165-82,618,165 DDIAS
    nsv5131698mobile element insertion1nstd203human GRCh38 chr11: 82,918,756-82,918,769 , GRCh37.p13 chr11: 82,629,798-82,629,811 DDIAS
    nsv4989093copy number variation1nstd200human GRCh38 chr11: 82,906,789-83,029,404 , GRCh37.p13 chr11: 82,617,831-82,740,446 RAB30, RPL7AP54, 1 more genes
    nsv4989092copy number variation1nstd200human GRCh38 chr11: 82,893,559-82,913,386 , GRCh37.p13 chr11: 82,604,601-82,624,428 PRCP, DDIAS
    nsv4843532copy number variation1nstd200human GRCh37 chr11: 82,604,601-82,624,428 , GRCh38.p12 chr11: 82,893,559-82,913,386 DDIAS, PRCP
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