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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074145inversion1nstd229human GRCh38 chr11: 104,112,094-113,544,164 , GRCh37.p13 chr11: 103,982,822-113,414,886 COLCA1, LOC105369491, 150 more genes
    nsv7072241inversion1nstd229human GRCh38 chr11: 110,457,672-110,457,823 , GRCh37.p13 chr11: 110,328,396-110,328,547 FDX1
    nsv7069281inversion1nstd229human GRCh38 chr11: 107,936,485-114,400,629 , GRCh37.p13 chr11: 107,807,211-114,271,351 LRRC37A13P, POU2AF3, 121 more genes
    nsv7065935inversion1nstd229human GRCh38 chr11: 107,044,115-113,544,291 , GRCh37.p13 chr11: 106,914,841-113,415,013 LINC02762, TIMM8B, 112 more genes
    nsv6912231copy number variation1nstd229human GRCh38 chr11: 110,421,608-110,430,627 , GRCh37.p13 chr11: 110,292,332-110,301,351 FDX1
    nsv6911917copy number variation1nstd229human GRCh38 chr11: 110,430,548-110,449,804 , GRCh37.p13 chr11: 110,301,272-110,320,528 FDX1
    nsv6908160copy number variation1nstd229human GRCh38 chr11: 110,433,209-110,435,608 , GRCh37.p13 chr11: 110,303,933-110,306,332 FDX1
    nsv6906990copy number variation1nstd229human GRCh38 chr11: 110,436,782-110,447,643 , GRCh37.p13 chr11: 110,307,506-110,318,367 FDX1
    nsv6901856copy number variation1nstd229human GRCh38 chr11: 110,391,986-111,106,264 , GRCh37.p13 chr11: 110,262,710-110,976,988 LOC105369489, LINC02550, 8 more genes
    nsv6899195copy number variation1nstd229human GRCh38 chr11: 110,436,917-110,440,641 , GRCh37.p13 chr11: 110,307,641-110,311,365 FDX1
    nsv6637811copy number variation1nstd102humanPathogenic GRCh37 chr11: 109,328,787-116,414,966 , GRCh38.p12 chr11: 109,458,061-116,544,249 LOC102723966, NXPE4, 129 more genes
    nsv6586218inversion1nstd223human GRCh38 chr11: 107,936,497-114,408,912 , GRCh37.p13 chr11: 107,807,223-114,279,634 LOC107984390, ATF4P4, 121 more genes
    nsv6470555copy number variation1nstd223human GRCh38 chr11: 110,436,781-110,447,642 , GRCh37.p13 chr11: 110,307,505-110,318,366 FDX1
    nsv6468357copy number variation1nstd223human GRCh38 chr11: 110,429,601-110,430,500 , GRCh37.p13 chr11: 110,300,325-110,301,224 FDX1
    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
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 more genes
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv6274662copy number variation1nstd214human GRCh38 chr11: 110,444,698-110,444,747 , GRCh37.p13 chr11: 110,315,422-110,315,471 FDX1
    nsv6273830copy number variation1nstd214human GRCh38 chr11: 110,444,667-110,444,744 , GRCh37.p13 chr11: 110,315,391-110,315,468 FDX1
    nsv6258334mobile element insertion1nstd215human GRCh38 chr11: 110,452,062-110,452,062 , GRCh37.p13 chr11: 110,322,786-110,322,786 FDX1
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