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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6714902copy number variation1nstd229human GRCh38 chr3: 23,948,461-23,948,554 , GRCh37.p13 chr3: 23,989,952-23,990,045 NR1D2
    nsv6709095copy number variation1nstd229human GRCh38 chr3: 23,962,834-23,962,943 , GRCh37.p13 chr3: 24,004,325-24,004,434 NR1D2
    nsv6700354copy number variation1nstd229human GRCh38 chr3: 23,948,851-23,956,102 , GRCh37.p13 chr3: 23,990,342-23,997,593 NR1D2
    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
    nsv6375062copy number variation1nstd223human GRCh38 chr3: 23,980,601-23,982,600 , GRCh37.p13 chr3: 24,022,092-24,024,091 NR1D2
    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
    nsv6253822mobile element insertion1nstd215human GRCh38 chr3: 23,957,408-23,957,408 , GRCh37.p13 chr3: 23,998,899-23,998,899 NR1D2
    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
    nsv6054727insertion1nstd212human GRCh38 chr3: 23,950,381-23,950,381 , GRCh37.p13 chr3: 23,991,872-23,991,872 NR1D2
    nsv5900737copy number variation1nstd209human GRCh38 chr3: 23,943,009-23,943,484 , GRCh37.p13 chr3: 23,984,500-23,984,975 NR1D2, NKIRAS1
    nsv5690949mobile element insertion1nstd211human GRCh38 chr3: 23,957,408-23,957,408 , GRCh37.p13 chr3: 23,998,899-23,998,899 NR1D2
    nsv5447873copy number variation1nstd206human GRCh38 chr3: 23,948,461-23,948,554 , GRCh37.p13 chr3: 23,989,952-23,990,045 NR1D2
    nsv5446712copy number variation1nstd206human GRCh38 chr3: 23,947,689-23,947,796 , GRCh37.p13 chr3: 23,989,180-23,989,287 NR1D2
    nsv5060925mobile element insertion1nstd203human GRCh38 chr3: 23,980,553-23,980,567 , GRCh37.p13 chr3: 24,022,044-24,022,058 NR1D2
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4796680copy number variation1nstd200human GRCh37 chr3: 23,984,524-23,984,976 , GRCh38.p12 chr3: 23,943,033-23,943,485 NKIRAS1, NR1D2
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