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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5705155mobile element insertion1nstd211human GRCh38 chr22: 37,301,709-37,301,709 , GRCh37.p13 chr22: 37,697,750-37,697,750 CYTH4, LOC105373024
    nsv5163665mobile element insertion1nstd203human GRCh38 chr22: 37,297,184-37,297,194 , GRCh37.p13 chr22: 37,693,225-37,693,235 CYTH4, LOC105373024
    nsv5038469copy number variation1nstd200human GRCh38 chr22: 37,288,046-37,288,143 , GRCh37.p13 chr22: 37,684,087-37,684,184 CYTH4
    nsv5037297copy number variation1nstd200human GRCh38 chr22: 37,315,730-37,315,887 , GRCh37.p13 chr22: 37,711,771-37,711,928 LOC105373024, CYTH4
    nsv5035087copy number variation1nstd200human GRCh38 chr22: 37,290,945-37,291,088 , GRCh37.p13 chr22: 37,686,986-37,687,129 CYTH4, LOC105373024
    nsv4872061copy number variation1nstd200human GRCh37 chr22: 37,711,771-37,711,928 , GRCh38.p12 chr22: 37,315,730-37,315,887 CYTH4, LOC105373024
    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
    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
    nsv4630469copy number variation1nstd183human GRCh37 chr22: 37,613,169-37,714,871 , GRCh38.p12 chr22: 37,217,129-37,318,830 LOC105373024, SSTR3, 3 more genes
    nsv4567612insertion1nstd166human GRCh37.p13 chr22: 37,677,267-37,677,267 , GRCh38.p12 chr22: 37,281,226-37,281,226 CYTH4
    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
    nsv4289065copy number variation1nstd166human GRCh37.p13 chr22: 37,686,986-37,687,129 , GRCh38.p12 chr22: 37,290,945-37,291,088 CYTH4, LOC105373024
    nsv4278013copy number variation1nstd166human GRCh37.p13 chr22: 37,381,892-38,500,309 , GRCh38.p12 chr22: 36,985,851-38,104,302 GGA1, GALR3, 46 more genes
    nsv3922128copy number variation1nstd102humanPathogenic GRCh37 chr22: 35,729,986-39,296,182 , NCBI36 chr22: 34,059,986-37,626,128 , GRCh38 chr22: 35,333,993-38,900,177 LOC102724378, CARD10, 120 more genes
    nsv3919881copy number variation1nstd102humanPathogenic GRCh37 chr22: 17,397,633-51,178,213 , GRCh38 chr22: 16,916,743-50,739,785 , NCBI36 chr22: 15,777,633-49,525,079 MIR12114, MIR6820, 1059 more genes
    nsv3919085copy number variation1nstd102humanPathogenic NCBI36 chr22: 17,008,132-49,591,432 , GRCh37.p13 chr22: 18,628,132-51,244,566 , GRCh38.p12 chr22: 18,145,365-50,806,138 IGLV2-28, LINC01310, 1023 more genes
    nsv3918055copy number variation1nstd102humanUncertain significance GRCh37 chr22: 37,300,872-37,951,517 , NCBI36 chr22: 35,630,818-36,281,463 , GRCh38 chr22: 36,904,830-37,555,510 LOC105373024, ELFN2, 21 more genes
    nsv3917356copy number variation1nstd102humanUncertain significance GRCh37 chr22: 37,520,289-37,976,764 , NCBI36 chr22: 35,850,235-36,306,710 , GRCh38 chr22: 37,124,249-37,580,757 C1QTNF6, LOC105373024, 12 more genes
    nsv3914747copy number variation1nstd102humanPathogenic NCBI36 chr22: 35,278,369-36,395,868 , GRCh38 chr22: 36,552,376-37,669,915 , GRCh37 chr22: 36,948,423-38,065,922 ELFN2, LGALS2, 35 more genes
    nsv3913775copy number variation1nstd102humanPathogenic NCBI36 chr22: 15,777,498-49,525,130 , GRCh38 chr22: 16,916,608-50,739,836 , GRCh37 chr22: 17,397,498-51,178,264 ZNF280A, RFPL1S, 1059 more genes
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