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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906695copy number variation1nstd209human GRCh38 chr3: 149,122,793-149,128,306 , GRCh37.p13 chr3: 148,840,580-148,846,093 HPS3
    nsv5889639copy number variation1nstd209human GRCh38 chr3: 149,166,254-149,166,800 , GRCh37.p13 chr3: 148,884,041-148,884,587 HPS3, CP
    nsv5834708copy number variation1nstd209human GRCh38 chr3: 149,122,810-149,128,108 , GRCh37.p13 chr3: 148,840,597-148,845,895 HPS3
    nsv5685204mobile element insertion1nstd211human GRCh38 chr3: 149,130,894-149,130,894 , GRCh37.p13 chr3: 148,848,681-148,848,681 HPS3
    nsv5673557copy number variation1nstd102humanPathogenic GRCh37 chr3: 148,847,511-148,847,747 , GRCh38.p12 chr3: 149,129,724-149,129,960 HPS3
    nsv5451791copy number variation1nstd206human GRCh38 chr3: 149,126,663-149,130,599 , GRCh37.p13 chr3: 148,844,450-148,848,386 HPS3
    nsv5447447copy number variation1nstd206human GRCh38 chr3: 149,166,254-149,166,806 , GRCh37.p13 chr3: 148,884,041-148,884,593 HPS3, CP
    nsv5446732copy number variation1nstd206human GRCh38 chr3: 149,123,369-149,138,129 , GRCh37.p13 chr3: 148,841,156-148,855,916 HPS3
    nsv5406008mobile element insertion1nstd206human GRCh38 chr3: 149,130,894-149,130,945 , GRCh37.p13 chr3: 148,848,681-148,848,732 HPS3
    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
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4912312copy number variation1nstd200human GRCh38 chr3: 149,166,254-149,166,806 , GRCh37.p13 chr3: 148,884,041-148,884,593 CP, HPS3
    nsv4797956copy number variation1nstd200human GRCh37 chr3: 148,884,041-148,884,593 , GRCh38.p12 chr3: 149,166,254-149,166,806 HPS3, CP
    nsv4791493copy number variation1nstd200human GRCh37 chr3: 148,844,500-148,848,396 , GRCh38.p12 chr3: 149,126,713-149,130,609 HPS3
    nsv4714455copy number variation1nstd195human GRCh37 chr3: 148,844,801-149,097,551 , GRCh38.p12 chr3: 149,127,014-149,379,764 , CP, 7 more genes
    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
    nsv4683682copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 148,859,072-148,859,177 , GRCh38.p12 chr3: 149,141,285-149,141,390 HPS3
    nsv4683405copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 148,856,981-148,858,808 , GRCh38 chr3: 149,139,194-149,141,021 HPS3
    nsv4682548copy number variation1nstd102humanUncertain significance GRCh37 chr3: 148,891,481-148,899,940 , GRCh38.p12 chr3: 149,173,694-149,182,153 HPS3, CP
    nsv4682141copy number variation1nstd102humanPathogenic GRCh37 chr3: 148,847,511-148,847,727 , GRCh38.p12 chr3: 149,129,724-149,129,940 HPS3
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