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Items: 1 to 20 of 210

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097523copy number variation2nstd102humanPathogenic GRCh37 chr5: 176,289,625-177,151,363 , GRCh38.p12 chr5: 176,862,624-177,724,362 PFN3, DBN1, 29 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
    nsv7096767copy number variation1nstd102humanUncertain significance GRCh37 chr5: 176,618,865-177,036,696 , GRCh38.p12 chr5: 177,191,864-177,609,695 PFN3, NSD1, 21 more genes
    nsv7050002inversion1nstd229human GRCh38 chr5: 175,906,338-177,936,522 , GRCh37.p13 chr5: 175,333,341-177,363,523 PRR7, OR1X5P, 60 more genes
    nsv7047250inversion1nstd229human GRCh38 chr5: 177,481,353-177,487,139 , GRCh37.p13 chr5: 176,908,354-176,914,140 PDLIM7
    nsv7042905inversion1nstd229human GRCh38 chr5: 177,489,945-177,523,841 , GRCh37.p13 chr5: 176,916,946-176,950,842 PDLIM7, FAM193B, 2 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
    nsv6791511copy number variation1nstd229human GRCh38 chr5: 177,484,190-177,488,066 , GRCh37.p13 chr5: 176,911,191-176,915,067 PDLIM7
    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
    nsv6636832copy number variation1nstd102humanUncertain significance GRCh37 chr5: 176,718,361-176,957,659 , GRCh38.p12 chr5: 177,291,360-177,530,658 PRR7-AS1, PFN3, 16 more genes
    nsv6636357copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 176,547,912-177,126,647 , GRCh38.p12 chr5: 177,120,911-177,699,646 DBN1, F12, 24 more genes
    nsv6636258copy number variation1nstd102humanUncertain significance GRCh37 chr5: 176,616,151-177,107,778 , GRCh38.p12 chr5: 177,189,150-177,680,777 RPL21P60, DBN1, 23 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
    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
    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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