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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5698204mobile element insertion2nstd211human GRCh38 chr11: 118,973,103-118,973,103 , GRCh37.p13 chr11: 118,843,813-118,843,813 FOXR1
    nsv5658423insertion1nstd207human GRCh38 chr11: 118,973,103-118,973,103 , GRCh37.p13 chr11: 118,843,813-118,843,813 FOXR1
    nsv5413996mobile element insertion1nstd206human GRCh38 chr11: 118,973,103-118,973,154 , GRCh37.p13 chr11: 118,843,813-118,843,864 FOXR1
    nsv5127895mobile element insertion1nstd203human GRCh38 chr11: 118,973,085-118,973,103 , GRCh37.p13 chr11: 118,843,795-118,843,813 FOXR1
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4722888insertion1nstd186human GRCh37 chr11: 118,843,795-118,843,795 , GRCh38.p12 chr11: 118,973,085-118,973,085 FOXR1
    nsv4683551copy number variation9nstd102humanUncertain significance, Pathogenic GRCh37 chr11: 117,856,768-118,972,385 , GRCh38.p12 chr11: 117,986,053-119,101,675 MIR6716, TREHP1, 48 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
    nsv4554080insertion1nstd166human GRCh37.p13 chr11: 118,843,795-118,843,795 , GRCh38.p12 chr11: 118,973,085-118,973,085 FOXR1
    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
    nsv4451218copy number variation1nstd102humanUncertain significance GRCh37 chr11: 118,007,722-119,170,511 , GRCh38.p12 chr11: 118,137,007-119,299,801 ABCG4, CCDC153, 52 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
    nsv4203619copy number variation1nstd166human GRCh37.p13 chr11: 118,840,985-118,842,634 , GRCh38.p12 chr11: 118,970,275-118,971,924 FOXR1
    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
    nsv3918358copy number variation1nstd102humanLikely benign NCBI36 chr11: 118,309,002-118,591,211 , GRCh38 chr11: 118,933,083-119,215,291 , GRCh37 chr11: 118,803,792-119,086,001 SLC37A4, ABCG4, 19 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
    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
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