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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5894678copy number variation1nstd209human GRCh38 chr5: 87,038,746-87,057,733 , GRCh37.p13 chr5: 86,334,563-86,353,550 LOC645261
    nsv5843237copy number variation1nstd209human GRCh38 chr5: 87,038,725-87,057,662 , GRCh37.p13 chr5: 86,334,542-86,353,479 LOC645261
    nsv5459904copy number variation1nstd206human GRCh38 chr5: 87,038,771-87,057,709 , GRCh37.p13 chr5: 86,334,588-86,353,526 LOC645261
    nsv5228190copy number variation1nstd204human GRCh38.p13 chr5: 87,041,979-87,056,365 , GRCh37.p13 chr5: 86,337,796-86,352,182 LOC645261
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4948993copy number variation1nstd200human GRCh38 chr5: 87,050,698-87,056,790 , GRCh37.p13 chr5: 86,346,515-86,352,607 LOC645261
    nsv4947049copy number variation1nstd200human GRCh38 chr5: 87,038,720-87,057,778 , GRCh37.p13 chr5: 86,334,537-86,353,595 LOC645261
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4793207copy number variation1nstd200human GRCh37 chr5: 86,334,584-86,353,560 , GRCh38.p12 chr5: 87,038,767-87,057,743 LOC645261
    nsv4675667copy number variation1nstd102humanPathogenic GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166 LOC101929380, LIX1-AS1, 318 more genes
    nsv4591801copy number variation1nstd183human GRCh37 chr5: 86,338,981-86,352,702 , GRCh38.p12 chr5: 87,043,164-87,056,885 LOC645261
    nsv4457339copy number variation1nstd102humanPathogenic GRCh37 chr5: 83,497,559-88,416,354 , GRCh38.p12 chr5: 84,201,741-89,120,537 LINC02144, NBPF22P, 47 more genes
    nsv4456926copy number variation1nstd102humanUncertain significance GRCh37 chr5: 85,607,233-86,539,904 , GRCh38.p12 chr5: 86,311,415-87,244,087 SNORD138, MIR4280, 11 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4328126inversion1nstd166human GRCh37.p13 chr5: 75,669,511-101,876,780 , GRCh38.p12 chr5: 76,373,686-102,541,076 , BHMT, 331 more genes
    nsv4124247copy number variation1nstd166human GRCh37.p13 chr5: 86,334,588-86,353,538 , GRCh38.p12 chr5: 87,038,771-87,057,721 LOC645261
    nsv3924896copy number variation1nstd102humanPathogenic GRCh38 chr5: 84,603,580-111,435,081 , GRCh37 chr5: 83,899,398-110,770,779 , NCBI36 chr5: 83,935,154-110,798,678 LOC107986438, GGCTP1, 254 more genes
    nsv3922083copy number variation1nstd102humanPathogenic GRCh38 chr5: 86,766,959-92,148,845 , GRCh37 chr5: 86,062,776-91,444,662 , NCBI36 chr5: 86,098,532-91,480,418 LOC107986387, RN7SL629P, 52 more genes
    nsv3920548copy number variation1nstd102humanPathogenic GRCh38 chr5: 86,343,721-88,779,835 , NCBI36 chr5: 85,675,295-88,111,408 , GRCh37 chr5: 85,639,539-88,075,652 RNU6-727P, TMEM161B-DT, 31 more genes
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