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Items: 1 to 20 of 277

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974579inversion1nstd209human GRCh38 chr2: 96,682,737-96,686,840 , GRCh37.p13 chr2: 97,348,474-97,352,577 FER1L5
    nsv5956846insertion1nstd209human GRCh38 chr2: 96,659,288-96,659,288 , GRCh37.p13 chr2: 97,325,025-97,325,025 FER1L5
    nsv5876678copy number variation1nstd209human GRCh38 chr2: 95,981,467-97,579,646 , GRCh37.p13 chr2: 96,647,215-98,196,109 , ARID5A, 48 more genes
    nsv5875449copy number variation1nstd209human GRCh38 chr2: 96,681,824-96,682,120 , GRCh37.p13 chr2: 97,347,561-97,347,857 FER1L5
    nsv5874943copy number variation1nstd209human GRCh38 chr2: 96,658,504-96,659,184 , GRCh37.p13 chr2: 97,324,241-97,324,921 FER1L5
    nsv5833537copy number variation1nstd209human GRCh38 chr2: 96,682,753-96,684,468 , GRCh37.p13 chr2: 97,348,490-97,350,205 FER1L5
    nsv5714548mobile element insertion1nstd211human GRCh38 chr2: 96,654,898-96,654,898 , GRCh37.p13 chr2: 97,320,635-97,320,635 FER1L5
    nsv5622377insertion1nstd207human GRCh38 chr2: 96,659,342-96,659,342 , GRCh37.p13 chr2: 97,325,079-97,325,079 FER1L5
    nsv5610022insertion1nstd207human GRCh38 chr2: 96,659,350-96,659,350 , GRCh37.p13 chr2: 97,325,087-97,325,087 FER1L5
    nsv5580654copy number variation1nstd207human GRCh38 chr2: 96,659,435-96,659,484 , GRCh37.p13 chr2: 97,325,172-97,325,221 FER1L5
    nsv5565173copy number variation1nstd207human GRCh38 chr2: 96,659,290-96,659,400 , GRCh37.p13 chr2: 97,325,027-97,325,137 FER1L5
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5452136copy number variation1nstd206human GRCh38 chr2: 96,678,362-96,678,704 , GRCh37.p13 chr2: 97,344,099-97,344,441 FER1L5
    nsv5446001copy number variation1nstd206human GRCh38 chr2: 96,691,885-96,724,476 , GRCh37.p13 chr2: 97,357,622-97,390,213 LMAN2L, FER1L5
    nsv5445900copy number variation1nstd206human GRCh38 chr2: 96,658,317-96,659,179 , GRCh37.p13 chr2: 97,324,054-97,324,916 FER1L5
    nsv5436014copy number variation1nstd206human GRCh38 chr2: 96,669,450-96,670,266 , GRCh37.p13 chr2: 97,335,187-97,336,003 FER1L5
    nsv5381491copy number variation1nstd102humanPathogenic GRCh37 chr2: 96,755,045-98,021,592 , GRCh38.p12 chr2: 96,089,297-97,285,797 LOC100421288, STARD7, 34 more genes
    nsv5381324copy number variation1nstd102humanPathogenic GRCh37 chr2: 96,737,083-98,193,473 , GRCh38.p12 chr2: 96,071,335-97,577,010 IGKV2OR2-8, LOC100506076, 42 more genes
    nsv5215020copy number variation1nstd204human GRCh38.p13 chr2: 96,060,101-97,188,600 , GRCh37.p13 chr2: 96,725,849-97,854,337 RN7SL313P, NCAPH, 33 more genes
    nsv5208747copy number variation1nstd204human GRCh38.p13 chr2: 96,686,819-96,688,218 , GRCh37.p13 chr2: 97,352,556-97,353,955 FER1L5
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