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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5949619insertion1nstd209human GRCh38 chr3: 161,438,914-161,438,914 , GRCh37.p13 chr3: 161,156,702-161,156,702 LINC02067
    nsv5692601mobile element insertion1nstd211human GRCh38 chr3: 161,425,965-161,425,965 , GRCh37.p13 chr3: 161,143,753-161,143,753 LINC02067
    nsv5606764insertion1nstd207human GRCh38 chr3: 161,438,914-161,438,914 , GRCh37.p13 chr3: 161,156,702-161,156,702 LINC02067
    nsv5560984sequence alteration1nstd206human GRCh37.p13 chr3: 161,086,425-162,243,749 , GRCh38 chr3: 161,368,637-162,525,961 OTOL1, SPTSSB, 6 more genes
    nsv5538574insertion1nstd206human GRCh38 chr3: 161,438,946-161,438,965 , GRCh37.p13 chr3: 161,156,734-161,156,753 LINC02067
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5099297mobile element insertion1nstd203human GRCh38 chr3: 161,443,825-161,443,834 , GRCh37.p13 chr3: 161,161,613-161,161,622 LINC02067
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4798256copy number variation1nstd200human GRCh37 chr3: 161,105,005-162,439,344 , GRCh38.p12 chr3: 161,387,217-162,721,556 OTOL1, RPL23AP42, 5 more genes
    nsv4762509insertion1nstd199human GRCh37 chr3: 161,156,722-161,156,722 , GRCh38.p12 chr3: 161,438,934-161,438,934 LINC02067
    nsv4728438copy number variation1nstd102humanUncertain significance GRCh37 chr3: 160,488,346-161,322,790 , GRCh38.p12 chr3: 160,770,558-161,605,002 PSMC1P7, EEF1GP4, 11 more genes
    nsv4723874insertion1nstd186human GRCh37 chr3: 161,156,702-161,156,702 , GRCh38.p12 chr3: 161,438,914-161,438,914 LINC02067
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 MTAPP1, PLS1, 339 more genes
    nsv4540303insertion1nstd166human GRCh37.p13 chr3: 161,156,702-161,156,702 , GRCh38.p12 chr3: 161,438,914-161,438,914 LINC02067
    nsv4521222copy number variation1nstd166human GRCh37.p13 chr3: 160,945,999-161,276,000 , GRCh38.p12 chr3: 161,228,211-161,558,212 LOC105374187, LOC112268450, 8 more genes
    nsv4469848mobile element insertion1nstd166human GRCh37.p13 chr3: 161,146,447-161,146,447 , GRCh38.p12 chr3: 161,428,659-161,428,659 LINC02067, RPL23AP42
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4327115inversion1nstd166human GRCh37.p13 chr3: 131,882,701-162,233,318 , GRCh38.p12 chr3: 132,163,857-162,515,530 , ATP1B3, 446 more genes
    nsv3922860copy number variation1nstd102humanUncertain significance GRCh37 chr3: 161,019,834-161,804,660 , NCBI36 chr3: 162,502,528-163,287,354 , GRCh38 chr3: 161,302,046-162,086,872 LOC107986150, PSMC1P7, 6 more genes
    nsv3919833copy number variation1nstd102humanPathogenic GRCh38 chr3: 158,141,556-172,788,324 , NCBI36 chr3: 159,342,039-173,988,808 , GRCh37 chr3: 157,859,345-172,506,114 NMD3, TRV-AAC1-1, 173 more genes
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