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Items: 1 to 20 of 169

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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
    nsv7069281inversion1nstd229human GRCh38 chr11: 107,936,485-114,400,629 , GRCh37.p13 chr11: 107,807,211-114,271,351 LRRC37A13P, POU2AF3, 121 more genes
    nsv7068895inversion1nstd229human GRCh38 chr11: 100,518,680-109,308,656 , GRCh37.p13 chr11: 100,389,411-109,179,383 LINC02719, RNA5SP349, 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
    nsv6915723copy number variation1nstd229human GRCh38 chr11: 108,461,871-108,473,259 , GRCh37.p13 chr11: 108,332,598-108,343,986 POGLUT3, C11orf65
    nsv6907718copy number variation1nstd229human GRCh38 chr11: 107,314,715-108,574,752 , GRCh37.p13 chr11: 107,185,441-108,445,479 SLN, SUCLG2P3, 18 more genes
    nsv6906629copy number variation1nstd229human GRCh38 chr11: 108,478,301-108,481,400 , GRCh37.p13 chr11: 108,349,028-108,352,127 POGLUT3
    nsv6903062copy number variation1nstd229human GRCh38 chr11: 108,432,901-108,478,500 , GRCh37.p13 chr11: 108,303,628-108,349,227 C11orf65, POGLUT3
    nsv6637687copy number variation1nstd102humanPathogenic GRCh37 chr11: 101,371,503-109,306,519 , GRCh38.p12 chr11: 101,500,772-109,435,793 GRIA4, MTND1P36, 111 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
    nsv6578547inversion1nstd223human GRCh38 chr11: 104,070,004-110,020,477 , GRCh37.p13 chr11: 103,940,732-109,891,203 ACAT1, RNU6-654P, 69 more genes
    nsv6473044copy number variation1nstd223human GRCh38 chr11: 108,497,601-108,499,900 , GRCh37.p13 chr11: 108,368,328-108,370,627 LOC112267909, POGLUT3
    nsv6462602copy number variation1nstd223human GRCh38 chr11: 108,470,832-108,473,294 , GRCh37.p13 chr11: 108,341,559-108,344,021 POGLUT3
    nsv6459754copy number variation1nstd223human GRCh38 chr11: 108,469,073-108,470,698 , GRCh37.p13 chr11: 108,339,800-108,341,425 POGLUT3, C11orf65
    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
    nsv6309021copy number variation2nstd102humanUncertain significance GRCh37 chr11: 107,992,334-108,464,263 , GRCh38.p12 chr11: 108,121,607-108,593,536 EXPH5, C11orf65, 5 more genes
    nsv6301130copy number variation1nstd186human GRCh37 chr11: 108,339,801-108,341,402 , GRCh38.p12 chr11: 108,469,074-108,470,675 POGLUT3, C11orf65
    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
    nsv6132070copy number variation1nstd213human GRCh37 chr11: 108,270,000-108,510,001 , GRCh38.p12 chr11: 108,399,273-108,639,274 EXPH5, POGLUT3, 2 more genes
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