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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097525copy number variation1nstd102humanUncertain significance GRCh37 chr5: 177,419,710-177,422,934 , GRCh38.p12 chr5|NT_187652.1: 127,555-130,779 , GRCh38.p12 chr5: 177,992,709-177,995,933 PROP1
    nsv7097268copy number variation1nstd102humanUncertain significance GRCh37 chr5: 177,419,710-177,578,014 , GRCh38.p12 chr5: 177,992,709-178,151,013 RPL19P9, RMND5B, 6 more genes
    nsv7097267copy number variation3nstd102humanUncertain significance GRCh37 chr5: 175,158,654-179,263,593 , GRCh38.p12 chr5: 175,731,651-179,836,593 LOC112267937, LMAN2, 122 more genes
    nsv7097135copy number variation1nstd102humanUncertain significance GRCh37 chr5: 177,031,160-178,414,004 , GRCh38.p12 chr5: 177,604,159-178,987,003 MSANTD5, COL23A1, 41 more genes
    nsv7041943inversion1nstd229human GRCh38 chr5: 176,986,483-178,673,578 , GRCh37.p13 chr5: 176,413,484-178,100,579 DBN1, LOC100419951, 54 more genes
    nsv7041901inversion1nstd229human GRCh38 chr5: 175,920,087-179,128,938 , GRCh37.p13 chr5: 175,347,090-178,555,939 LOC100288803, NHP2, 98 more genes
    nsv7040659inversion1nstd229human GRCh38 chr5: 174,927,732-178,443,561 , GRCh37.p13 chr5: 174,354,735-177,870,562 RN7SKP148, FAM193B-DT, 90 more genes
    nsv7038290inversion1nstd229human GRCh38 chr5: 172,489,078-179,485,008 , GRCh37.p13 chr5: 171,916,082-178,912,009 ZFP2, NHP2, 168 more genes
    nsv6788306copy number variation1nstd229human GRCh38 chr5: 177,990,710-177,991,286 , GRCh37.p13 chr5: 177,417,711-177,418,287 PROP1
    nsv6636855copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 176,516,440-177,773,252 , GRCh38.p12 chr5: 177,089,439-178,346,251 DBN1, F12, 47 more genes
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 287 more genes
    nsv6630508copy number variation1nstd224human GRCh37 chr5: 177,408,429-177,422,908 , GRCh38.p12 chr5: 177,981,428-177,995,907 , GRCh38.p12 chr5|NT_187546.1: 120,009-131,892 , GRCh38.p12 chr5|NT_187652.1: 116,244-130,753 PROP1
    nsv6630316copy number variation2nstd224human GRCh37 chr5: 177,373,622-177,507,767 , GRCh38.p12 chr5: 177,946,621-178,080,766 PROP1, SUDS3P1, 4 more genes
    nsv6630315copy number variation1nstd224human GRCh37 chr5: 177,266,026-177,573,274 , GRCh38.p12 chr5: 177,839,025-178,146,273 SUDS3P1, RPL19P9, 9 more genes
    nsv6630314copy number variation1nstd224human GRCh37 chr5: 177,135,730-177,867,175 , GRCh38.p12 chr5: 177,708,729-178,440,174 SUDS3P1, MRPL50P3, 24 more genes
    nsv6630130copy number variation1nstd224human GRCh37 chr5: 176,898,619-177,507,767 , GRCh38.p12 chr5: 177,471,618-178,080,766 DDX41, SUDS3P1, 20 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6312189copy number variation1nstd102humanUncertain significance GRCh37 chr5: 176,047,812-177,422,934 , GRCh38.p12 chr5: 176,620,811-177,995,933 PFN3, UIMC1, 42 more genes
    nsv6296741copy number variation1nstd186human GRCh37 chr5: 177,096,325-178,737,001 , GRCh38.p12 chr5: 177,669,324-179,310,000 , ADAMTS2, 48 more genes
    nsv6291240copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 176,497,464-177,776,599 , GRCh38.p12 chr5: 177,070,463-178,349,598 DBN1, F12, 48 more genes
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