U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 512

    loading data ...

    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
    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
    nsv7050002inversion1nstd229human GRCh38 chr5: 175,906,338-177,936,522 , GRCh37.p13 chr5: 175,333,341-177,363,523 PRR7, OR1X5P, 60 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
    nsv6792238copy number variation1nstd229human GRCh38 chr5: 177,710,101-177,711,400 , GRCh37.p13 chr5: 177,137,102-177,138,401 FAM153A, LOC107986489
    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
    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
    nsv6635594copy number variation1nstd227human GRCh37 chr5: 177,135,730-177,376,317 , GRCh38.p12 chr5: 177,708,729-177,949,316 FAM153A, OR1X5P, 6 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
    nsv6630565copy number variation1nstd224human GRCh37 chr5: 177,005,613-177,222,590 , GRCh38.p12 chr5: 177,578,612-177,795,589 B4GALT7, TMED9, 4 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
    nsv6298188copy number variation1nstd186human GRCh37 chr5: 177,150,001-177,156,325 , GRCh38.p12 chr5: 177,723,000-177,729,324 LOC107986489, FAM153A
    nsv6296741copy number variation1nstd186human GRCh37 chr5: 177,096,325-178,737,001 , GRCh38.p12 chr5: 177,669,324-179,310,000 , ADAMTS2, 48 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center