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Items: 1 to 20 of 83

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv6915591copy number variation1nstd229human GRCh38 chr11: 60,848,131-60,852,519 , GRCh37.p13 chr11: 60,615,604-60,619,992 PTGDR2, CCDC86
    nsv6913154copy number variation1nstd229human GRCh38 chr11: 60,773,126-60,850,850 , GRCh37.p13 chr11: 60,540,599-60,618,323 MS4A15, PTGDR2, 3 more genes
    nsv6912097copy number variation1nstd229human GRCh38 chr11: 60,841,201-60,843,800 , GRCh37.p13 chr11: 60,608,674-60,611,273 CCDC86
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6902105copy number variation1nstd229human GRCh38 chr11: 60,850,968-60,858,187 , GRCh37.p13 chr11: 60,618,441-60,625,660 PTGDR2, CCDC86
    nsv6474481copy number variation1nstd223human GRCh38 chr11: 60,851,201-60,853,600 , GRCh37.p13 chr11: 60,618,674-60,621,073 PTGDR2, CCDC86
    nsv6465312copy number variation1nstd223human GRCh38 chr11: 60,838,661-60,840,411 , GRCh37.p13 chr11: 60,606,134-60,607,884 CCDC86
    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
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv5506058copy number variation1nstd206human GRCh38 chr11: 60,838,493-60,840,376 , GRCh37.p13 chr11: 60,605,966-60,607,849 CCDC86
    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
    nsv5325627inversion1nstd204human GRCh37.p13 chr11: 58,669,453-61,321,541 , GRCh38.p13 chr11: 58,901,980-61,554,069 , CD5, 118 more genes
    nsv4984989copy number variation1nstd200human GRCh38 chr11: 60,838,394-60,840,488 , GRCh37.p13 chr11: 60,605,867-60,607,961 CCDC86
    nsv4885672inversion1nstd200human GRCh37 chr11: 58,669,461-61,321,541 , GRCh38.p12 chr11: 58,901,988-61,554,069 , MS4A2, 118 more genes
    nsv4831656copy number variation1nstd200human GRCh37 chr11: 60,605,867-60,607,961 , GRCh38.p12 chr11: 60,838,394-60,840,488 CCDC86
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
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