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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv7093933copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 65,325,080-65,639,825 , GRCh38.p12 chr11: 65,557,609-65,872,354 ZNRD2-DT, ZNRD2, 22 more genes
    nsv7062888inversion1nstd229human GRCh38 chr11: 65,331,143-66,048,384 , GRCh37.p13 chr11: 65,098,614-65,815,855 FAUP4, MAP3K11, 50 more genes
    nsv7061449inversion1nstd229human GRCh38 chr11: 65,331,281-66,115,058 , GRCh37.p13 chr11: 65,098,752-65,882,529 LOC100420020, LINC02736, 53 more genes
    nsv6917808copy number variation1nstd229human GRCh38 chr11: 65,582,765-65,597,627 , GRCh37.p13 chr11: 65,350,236-65,365,098 KCNK7, EHBP1L1, 1 more genes
    nsv6912389copy number variation1nstd229human GRCh38 chr11: 65,604,598-65,954,847 , GRCh37.p13 chr11: 65,372,069-65,722,318 RNASEH2C, C11orf68, 24 more genes
    nsv6911951copy number variation1nstd229human GRCh38 chr11: 65,590,601-65,605,800 , GRCh37.p13 chr11: 65,358,072-65,373,271 KCNK7, MAP3K11, 1 more genes
    nsv6911106copy number variation1nstd229human GRCh38 chr11: 65,607,301-65,618,300 , GRCh37.p13 chr11: 65,374,772-65,385,771 PCNX3, MAP3K11
    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
    nsv6469340copy number variation1nstd223human GRCh38 chr11: 65,603,701-65,605,000 , GRCh37.p13 chr11: 65,371,172-65,372,471 MAP3K11
    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
    nsv6314192copy number variation1nstd102humanUncertain significance GRCh37 chr11: 64,935,724-66,405,514 , GRCh38.p12 chr11: 65,168,253-66,638,043 CNIH2, GAL3ST3, 95 more genes
    nsv6309121copy number variation2nstd102humanPathogenic GRCh37 chr11: 64,522,783-66,283,694 , GRCh38.p12 chr11: 64,755,311-66,516,223 SF3B2, ZNRD2-DT, 124 more genes
    nsv6275153copy number variation1nstd214human GRCh38 chr11: 65,596,839-65,596,913 , GRCh37.p13 chr11: 65,364,310-65,364,384 MAP3K11
    nsv6132269copy number variation1nstd213human GRCh37 chr11: 64,390,000-65,950,001 , GRCh38.p12 chr11: 64,622,528-66,182,530 MRPL49, CTSW, 103 more genes
    nsv6132112copy number variation1nstd213human GRCh37 chr11: 64,220,000-68,010,001 , GRCh38.p12 chr11: 64,452,528-68,242,533 ACTN3, ALDH3B1, 212 more genes
    nsv6080997insertion1nstd212human GRCh38 chr11: 65,609,333-65,609,333 , GRCh37.p13 chr11: 65,376,804-65,376,804 MAP3K11
    nsv6029410copy number variation1nstd212human GRCh38 chr11: 65,596,815-65,596,891 , GRCh37.p13 chr11: 65,364,286-65,364,362 MAP3K11
    nsv5921184copy number variation1nstd209human GRCh38 chr11: 65,596,834-65,596,912 , GRCh37.p13 chr11: 65,364,305-65,364,383 MAP3K11
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