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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5949511copy number variation1nstd209human GRCh38 chr22: 41,609,532-41,609,825 , GRCh37.p13 chr22: 42,005,536-42,005,829 DESI1
    nsv5669225insertion1nstd207human GRCh38 chr22: 41,610,080-41,610,080 , GRCh37.p13 chr22: 42,006,084-42,006,084 DESI1
    nsv5549198copy number variation1nstd206human GRCh38 chr22: 41,574,318-41,606,433 , GRCh37.p13 chr22: 41,970,322-42,002,437 CSDC2, DESI1, 1 more genes
    nsv5299062copy number variation1nstd204human GRCh38.p13 chr22: 41,442,501-41,665,900 , GRCh37.p13 chr22: 41,838,505-42,061,904 CSDC2, LOC105373043, 8 more genes
    nsv5281292copy number variation1nstd204human GRCh38.p13 chr22: 41,124,301-41,900,100 , GRCh37.p13 chr22: 41,520,305-42,296,104 SNU13, RANGAP1, 34 more genes
    nsv5038827copy number variation1nstd200human GRCh38 chr22: 41,566,331-41,606,492 , GRCh37.p13 chr22: 41,962,335-42,002,496 DESI1, CSDC2, 1 more genes
    nsv5032425inversion1nstd200human GRCh38 chr22: 41,452,969-44,153,937 , GRCh37.p13 chr22: 41,848,973-44,549,817 , LOC101927393, 95 more genes
    nsv5031981copy number variation1nstd200human GRCh38 chr22: 41,585,527-41,599,747 , GRCh37.p13 chr22: 41,981,531-41,995,751 PMM1, DESI1
    nsv5031946copy number variation1nstd200human GRCh38 chr22: 41,609,084-41,611,719 , GRCh37.p13 chr22: 42,005,088-42,007,723 DESI1
    nsv4888026copy number variation1nstd200human GRCh37 chr22: 41,970,322-42,002,437 , GRCh38.p12 chr22: 41,574,318-41,606,433 DESI1, CSDC2, 1 more genes
    nsv4881875copy number variation1nstd200human GRCh37 chr22: 42,005,088-42,007,723 , GRCh38.p12 chr22: 41,609,084-41,611,719 DESI1
    nsv4873468copy number variation1nstd200human GRCh37 chr22: 41,991,758-41,992,161 , GRCh38.p12 chr22: 41,595,754-41,596,157 DESI1
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4729846copy number variation1nstd102humanUncertain significance GRCh37 chr22: 41,853,620-42,385,978 , GRCh38.p12 chr22: 41,457,616-41,989,974 RNU6ATAC22P, CSDC2, 23 more genes
    nsv4676292copy number variation1nstd102humanPathogenic GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410 PDXP-DT, PDGFB, 550 more genes
    nsv4676232copy number variation1nstd102humanPathogenic GRCh37 chr22: 40,502,364-51,197,838 , GRCh38.p12 chr22: 40,106,360-50,759,410 MIR378I, SNORD13P1, 274 more genes
    nsv4676125copy number variation1nstd102humanUncertain significance GRCh37 chr22: 41,871,935-42,026,428 , GRCh38.p12 chr22: 41,475,931-41,630,424 LOC105373044, ACO2, 5 more genes
    nsv4628998copy number variation1nstd183human GRCh37 chr22: 42,016,995-42,017,379 , GRCh38.p12 chr22: 41,620,991-41,621,375 DESI1, XRCC6
    nsv4627559copy number variation1nstd183human GRCh37 chr22: 41,996,640-42,021,638 , GRCh38.p12 chr22: 41,600,636-41,625,634 DESI1, XRCC6
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 IGLV3-27, XKR3, 1082 more genes
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