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 160

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7056901inversion1nstd229human GRCh38 chr5: 178,724,559-178,724,593 , GRCh37.p13 chr5: 178,151,560-178,151,594 ZNF354A
    nsv7041901inversion1nstd229human GRCh38 chr5: 175,920,087-179,128,938 , GRCh37.p13 chr5: 175,347,090-178,555,939 LOC100288803, NHP2, 98 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
    nsv6795952copy number variation1nstd229human GRCh38 chr5: 178,722,629-178,725,699 , GRCh37.p13 chr5: 178,149,630-178,152,700 ZNF354A
    nsv6795790copy number variation1nstd229human GRCh38 chr5: 178,442,220-179,237,764 , GRCh37.p13 chr5: 177,869,221-178,664,765 LOC100288803, RN7SKP70, 18 more genes
    nsv6788065copy number variation1nstd229human GRCh38 chr5: 178,651,183-179,054,533 , GRCh37.p13 chr5: 178,078,184-178,481,534 GRM6, RNU1-39P, 13 more genes
    nsv6781251copy number variation1nstd229human GRCh38 chr5: 178,256,072-179,080,937 , GRCh37.p13 chr5: 177,683,073-178,507,938 ZNF354B, ZNF354A, 20 more genes
    nsv6780844copy number variation1nstd229human GRCh38 chr5: 178,693,345-178,777,486 , GRCh37.p13 chr5: 178,120,346-178,204,487 AACSP1, MSANTD5, 1 more genes
    nsv6780522copy number variation1nstd229human GRCh38 chr5: 178,424,750-178,866,017 , GRCh37.p13 chr5: 177,851,751-178,293,018 ZNF354A, ZNF354B, 8 more genes
    nsv6779592copy number variation1nstd229human GRCh38 chr5: 178,725,807-178,726,129 , GRCh37.p13 chr5: 178,152,808-178,153,130 ZNF354A
    nsv6778868copy number variation1nstd229human GRCh38 chr5: 178,408,171-178,917,083 , GRCh37.p13 chr5: 177,835,172-178,344,084 ZFP2, RN7SKP70, 11 more genes
    nsv6636731copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,125,235-178,759,093 , GRCh38.p12 chr5: 178,698,234-179,332,092 LOC100422593, ZNF879, 14 more genes
    nsv6636440copy number variation1nstd102humanUncertain significance GRCh37 chr5: 177,746,012-179,975,280 , GRCh38.p12 chr5: 178,319,011-180,548,280 RUFY1-AS1, RPS15AP18, 60 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
    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
    nsv6313755copy number variation1nstd102humanUncertain significance GRCh37 chr5: 177,954,576-180,198,875 , GRCh38.p12 chr5: 178,527,575-180,771,875 MIR340, RASGEF1C, 64 more genes
    nsv6313622copy number variation1nstd102humanUncertain significance GRCh37 chr5: 177,926,393-178,613,706 , GRCh38.p12 chr5: 178,499,392-179,186,705 RN7SKP70, ADAMTS2, 18 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
    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