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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
    nsv7147377copy number variation1nstd232human GRCh37.p13 chr11: 67,803,846-67,803,925 , GRCh38.p12 chr11: 68,036,379-68,036,458 NDUFS8
    nsv7138026copy number variation1nstd232human GRCh37.p13 chr11: 67,800,477-67,800,574 , GRCh38.p12 chr11: 68,033,010-68,033,107 NDUFS8, MIR4691, 1 more genes
    nsv7094099copy number variation1nstd102humanUncertain significance GRCh37 chr11: 67,759,017-68,216,538 , GRCh38.p12 chr11: 67,991,546-68,449,070 LRP5, UNC93B1, 11 more genes
    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
    nsv7075597inversion1nstd229human GRCh38 chr11: 68,033,455-68,052,741 , GRCh37.p13 chr11: 67,800,922-67,820,208 NDUFS8, MIR4691, 3 more genes
    nsv7075540inversion1nstd229human GRCh38 chr11: 67,968,443-71,626,784 , GRCh37.p13 chr11: 67,735,914-71,337,830 S100A11P3, CCND1, 76 more genes
    nsv7068248inversion1nstd229human GRCh38 chr11: 68,036,364-68,036,472 , GRCh37.p13 chr11: 67,803,831-67,803,939 NDUFS8
    nsv7063416inversion1nstd229human GRCh38 chr11: 67,577,505-68,052,740 , GRCh37.p13 chr11: 67,344,976-67,820,207 ALDH3B1, FAM86C2P, 30 more genes
    nsv6912757copy number variation1nstd229human GRCh38 chr11: 66,793,001-68,121,500 , GRCh37.p13 chr11: 66,560,472-67,888,967 CHKA-DT, LOC107984341, 66 more genes
    nsv6911763copy number variation1nstd229human GRCh38 chr11: 67,577,408-68,033,450 , GRCh37.p13 chr11: 67,344,879-67,800,917 LINC02754, LOC112268076, 27 more genes
    nsv6911508copy number variation1nstd229human GRCh38 chr11: 67,541,590-68,051,961 , GRCh37.p13 chr11: 67,309,061-67,819,428 NDUFV1, ENPP7P7, 30 more genes
    nsv6911163copy number variation1nstd229human GRCh38 chr11: 68,035,176-68,035,858 , GRCh37.p13 chr11: 67,802,643-67,803,325 NDUFS8
    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
    nsv6905813copy number variation1nstd229human GRCh38 chr11: 67,694,101-68,081,300 , GRCh37.p13 chr11: 67,461,572-67,848,767 OR7E1P, UNC93B5, 21 more genes
    nsv6469517copy number variation1nstd223human GRCh38 chr11: 68,034,801-68,035,600 , GRCh37.p13 chr11: 67,802,268-67,803,067 NDUFS8
    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
    nsv6132115copy number variation1nstd213human GRCh37 chr11: 67,280,000-68,040,001 , GRCh38.p12 chr11: 67,512,529-68,272,533 C11orf24, DOC2GP, 35 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
    nsv6022957copy number variation1nstd212human GRCh38 chr11: 68,034,848-68,035,796 , GRCh37.p13 chr11: 67,802,315-67,803,263 NDUFS8
    nsv5922883copy number variation1nstd209human GRCh38 chr11: 68,034,843-68,035,791 , GRCh37.p13 chr11: 67,802,310-67,803,258 NDUFS8
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