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Items: 1 to 20 of 184

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094100copy number variation1nstd102humanPathogenic GRCh37 chr11: 67,816,336-67,818,296 , GRCh38.p12 chr11: 68,048,869-68,050,829 TCIRG1
    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
    nsv7093252copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 67,809,262-67,809,435 , GRCh38 chr11: 68,041,795-68,041,968 TCIRG1
    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
    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
    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
    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
    nsv6904987copy number variation1nstd229human GRCh38 chr11: 68,040,736-68,045,304 , GRCh37.p13 chr11: 67,808,203-67,812,771 TCIRG1, MIR6753
    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
    nsv6309446copy number variation1nstd102humanPathogenic GRCh37 chr11: 67,814,890-67,818,296 , GRCh38.p12 chr11: 68,047,423-68,050,829 TCIRG1
    nsv6309232copy number variation1nstd102humanPathogenic GRCh37 chr11: 67,814,890-67,815,449 , GRCh38.p12 chr11: 68,047,423-68,047,982 TCIRG1
    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
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5274366copy number variation1nstd204human GRCh37.p13 chr11: 67,774,371-67,862,467 , GRCh38.p13 chr11: 68,006,901-68,095,000 ALDH3B1, CHKA, 5 more genes
    nsv4979961copy number variation1nstd200human GRCh38 chr11: 68,047,168-68,048,383 , GRCh37.p13 chr11: 67,814,635-67,815,850 TCIRG1
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