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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5715590mobile element insertion1nstd211human GRCh38 chr11: 119,313,727-119,313,727 , GRCh37.p13 chr11: 119,184,437-119,184,437 MCAM
    nsv5556165mobile element insertion1nstd206human GRCh38 chr11: 119,313,727-119,313,778 , GRCh37.p13 chr11: 119,184,437-119,184,488 MCAM
    nsv5506805copy number variation1nstd206human GRCh38 chr11: 119,311,421-119,311,496 , GRCh37.p13 chr11: 119,182,131-119,182,206 MCAM, MIR6756
    nsv5380954copy number variation1nstd102humanUncertain significance GRCh37 chr11: 119,077,108-120,133,495 , GRCh38.p12 chr11: 119,206,398-120,262,786 NECTIN1-DT, RNU6-262P, 29 more genes
    nsv4980965copy number variation1nstd200human GRCh38 chr11: 119,317,352-119,319,375 , GRCh37.p13 chr11: 119,188,062-119,190,085 MCAM
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4675236copy number variation1nstd102humanUncertain significance GRCh37 chr11: 118,280,670-119,650,105 , GRCh38.p12 chr11: 118,409,955-119,779,396 SETP16, UPK2, 59 more genes
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
    nsv4616371copy number variation1nstd183human GRCh37 chr11: 119,185,374-119,185,418 , GRCh38.p12 chr11: 119,314,664-119,314,708 MCAM
    nsv4455281copy number variation1nstd102humanPathogenic GRCh37 chr11: 117,830,263-134,938,470 , GRCh38.p12 chr11: 117,959,548-135,068,576 NTM-AS1, LOC403312, 369 more genes
    nsv4349506copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,691,675-134,889,485 , GRCh38.p12 chr11: 116,820,959-135,019,591 LOC107984407, DCPS, 394 more genes
    nsv4349045copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,700,253-134,904,063 , GRCh38.p12 chr11: 116,829,537-135,034,169 MPZL3, ADAMTS8, 393 more genes
    nsv4197842copy number variation1nstd166human GRCh37.p13 chr11: 119,182,131-119,182,206 , GRCh38.p12 chr11: 119,311,421-119,311,496 MCAM, MIR6756
    nsv3964674insertion1nstd168human GRCh37.p13 chr11: 119,174,240-119,235,317 , GRCh38 chr11: 119,303,530-119,364,607 CBL, MCAM, 5 more genes
    nsv3923375copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,722,088-134,868,420 , NCBI36 chr11: 116,227,298-134,373,630 , GRCh38 chr11: 116,851,372-134,998,526 VPS26B, LOC105369531, 390 more genes
    nsv3922253copy number variation1nstd102humanPathogenic GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246 RPS27P19, UBASH3B, 655 more genes
    nsv3916857copy number variation2nstd102humanPathogenic NCBI36 chr11: 116,227,321-134,373,617 , GRCh37 chr11: 116,722,111-134,868,407 , GRCh38 chr11: 116,851,395-134,998,513 RPUSD4, ELOCP22, 390 more genes
    nsv3916826copy number variation1nstd102humanPathogenic NCBI36 chr11: 118,559,939-134,452,384 , GRCh37.p13 chr11: 119,054,729-134,946,516 , GRCh38.p12 chr11: 119,184,020-135,076,622 NECTIN1-DT, TP53AIP1, 317 more genes
    nsv3915068copy number variation1nstd102humanPathogenic NCBI36 chr11: 118,165,684-134,373,617 , GRCh37 chr11: 118,660,474-134,868,407 , GRCh38 chr11: 118,789,765-134,998,513 GSEC, LOC399975, 337 more genes
    nsv3913230copy number variation1nstd102humanPathogenic GRCh38 chr11: 113,444,446-120,648,921 , NCBI36 chr11: 112,820,378-120,024,840 , GRCh37 chr11: 113,315,168-120,519,630 ARHGEF12, LOC105369526, 169 more genes
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