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Items: 1 to 20 of 238

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6717832copy number variation1nstd229human GRCh38 chr3: 23,903,965-23,908,993 , GRCh37.p13 chr3: 23,945,456-23,950,484 NKIRAS1
    nsv6716868copy number variation1nstd229human GRCh38 chr3: 23,901,044-23,906,413 , GRCh37.p13 chr3: 23,942,535-23,947,904 NKIRAS1
    nsv6716714copy number variation1nstd229human GRCh38 chr3: 23,893,375-23,897,343 , GRCh37.p13 chr3: 23,934,866-23,938,834 NKIRAS1
    nsv6715349copy number variation1nstd229human GRCh38 chr3: 23,767,217-24,101,093 , GRCh37.p13 chr3: 23,808,708-24,142,584 ARL4AP4, UBE2E1-AS1, 6 more genes
    nsv6634367copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,836,340-25,357,427 , GRCh38.p12 chr3: 13,794,843-25,315,936 TMEM43, SLC6A6, 132 more genes
    nsv6629003copy number variation1nstd224human GRCh37 chr3: 23,982,330-24,006,336 , GRCh38.p12 chr3: 23,940,839-23,964,845 NR1D2, NKIRAS1
    nsv6555215inversion1nstd223human GRCh38 chr3: 23,905,948-23,906,919 , GRCh37.p13 chr3: 23,947,439-23,948,410 NKIRAS1
    nsv6551685inversion1nstd223human GRCh38 chr3: 23,928,728-23,929,722 , GRCh37.p13 chr3: 23,970,219-23,971,213 NKIRAS1
    nsv6549677inversion1nstd223human GRCh38 chr3: 23,905,878-23,907,143 , GRCh37.p13 chr3: 23,947,369-23,948,634 NKIRAS1
    nsv6549002inversion1nstd223human GRCh38 chr3: 23,909,291-23,910,129 , GRCh37.p13 chr3: 23,950,782-23,951,620 NKIRAS1
    nsv6547349inversion1nstd223human GRCh38 chr3: 23,925,631-23,926,112 , GRCh37.p13 chr3: 23,967,122-23,967,603 NKIRAS1
    nsv6539751inversion1nstd223human GRCh38 chr3: 23,911,293-23,912,017 , GRCh37.p13 chr3: 23,952,784-23,953,508 NKIRAS1
    nsv6358154copy number variation1nstd223human GRCh38 chr3: 23,892,279-23,892,839 , GRCh37.p13 chr3: 23,933,770-23,934,330 NKIRAS1
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv6135011copy number variation1nstd213human GRCh37 chr3: 23,210,000-24,090,001 , GRCh38.p12 chr3: 23,168,509-24,048,510 RPL15, UBE2E1, 9 more genes
    nsv5900737copy number variation1nstd209human GRCh38 chr3: 23,943,009-23,943,484 , GRCh37.p13 chr3: 23,984,500-23,984,975 NR1D2, NKIRAS1
    nsv5725330mobile element insertion1nstd211human GRCh38 chr3: 23,913,064-23,913,064 , GRCh37.p13 chr3: 23,954,555-23,954,555 NKIRAS1
    nsv5206784mobile element deletion1nstd204human GRCh38.p13 chr3: 23,911,759-23,912,071 , GRCh37.p13 chr3: 23,953,250-23,953,562 NKIRAS1
    nsv5181224mobile element insertion1nstd203human GRCh38 chr3: 23,930,502-23,930,548 , GRCh37.p13 chr3: 23,971,993-23,972,039 NKIRAS1
    nsv5074336mobile element insertion1nstd203human GRCh38 chr3: 23,933,658-23,933,672 , GRCh37.p13 chr3: 23,975,149-23,975,163 NKIRAS1
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