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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093917copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,103,876-112,104,288 , GRCh38.p12 chr11: 112,233,153-112,233,565 RPS6P16, PTS
    nsv7093669copy number variation2nstd102humanUncertain significance GRCh37 chr11: 111,171,709-112,104,278 , GRCh38.p12 chr11: 111,300,984-112,233,555 CRYAB, RPS6P16, 43 more genes
    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
    nsv7065935inversion1nstd229human GRCh38 chr11: 107,044,115-113,544,291 , GRCh37.p13 chr11: 106,914,841-113,415,013 LINC02762, TIMM8B, 112 more genes
    nsv6915249copy number variation1nstd229human GRCh38 chr11: 112,198,427-112,225,388 , GRCh37.p13 chr11: 112,069,150-112,096,111 BCO2, MRPS36P4, 2 more genes
    nsv6906442copy number variation1nstd229human GRCh38 chr11: 112,225,709-112,229,242 , GRCh37.p13 chr11: 112,096,432-112,099,965 PTS
    nsv6900237copy number variation1nstd229human GRCh38 chr11: 112,196,001-112,247,900 , GRCh37.p13 chr11: 112,066,724-112,118,623 RPS12P21, PTS, 4 more genes
    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
    nsv6620697copy number variation1nstd224human GRCh37 chr11: 112,064,216-112,362,462 , GRCh38.p12 chr11: 112,193,493-112,491,739 MRPS36P4, PLET1, 12 more genes
    nsv6620695copy number variation1nstd224human GRCh37 chr11: 111,953,288-112,208,967 , GRCh38.p12 chr11: 112,082,564-112,338,244 TIMM8B, NKAPD1, 15 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
    nsv6474741copy number variation1nstd223human GRCh38 chr11: 112,201,101-112,236,800 , GRCh37.p13 chr11: 112,071,824-112,107,523 RPS6P16, PTS, 3 more genes
    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
    nsv6309034copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,097,157-112,104,288 , GRCh38.p12 chr11: 112,226,434-112,233,565 RPS6P16, PTS
    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
    nsv6132074copy number variation1nstd213human GRCh37 chr11: 112,030,000-112,490,001 , GRCh38.p12 chr11: 112,159,277-112,619,278 BCO2, KCTD9P4, 17 more genes
    nsv5672778copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,096,088-112,105,696 , GRCh38.p12 chr11: 112,225,365-112,234,973 RPS6P16, PTS
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
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