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 92

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv6732675copy number variation1nstd229human GRCh38 chr4: 52,191,024-52,824,366 , GRCh37.p13 chr4: 53,057,190-53,690,533 LOC107986279, USP46-DT, 9 more genes
    nsv6724910copy number variation1nstd229human GRCh38 chr4: 52,549,568-52,825,492 , GRCh37.p13 chr4: 53,415,734-53,691,659 DANCR, SNORA26, 6 more genes
    nsv6637063copy number variation1nstd102humanUncertain significance GRCh37 chr4: 52,685,980-59,272,025 , GRCh38.p12 chr4: 51,819,814-58,405,859 SPINK2, RN7SL492P, 100 more genes
    nsv6637004copy number variation1nstd102humanUncertain significance GRCh37 chr4: 53,098,544-53,949,065 , GRCh38.p12 chr4: 52,232,378-53,082,898 LINC01618, LOC107986279, 12 more genes
    nsv6636907copy number variation1nstd102humanUncertain significance GRCh37 chr4: 53,434,611-54,079,547 , GRCh38.p12 chr4: 52,568,445-53,213,380 USP46, LOC107986281, 9 more genes
    nsv6376992copy number variation1nstd223human GRCh38 chr4: 52,658,201-52,660,900 , GRCh37.p13 chr4: 53,524,368-53,527,067 USP46, USP46-DT
    nsv6313624copy number variation1nstd102humanUncertain significance GRCh37 chr4: 53,091,609-53,953,124 , GRCh38.p12 chr4: 52,225,443-53,086,957 LOC100419861, RASL11B, 12 more genes
    nsv6313491copy number variation1nstd102humanUncertain significance GRCh37 chr4: 53,435,144-54,091,178 , GRCh38.p12 chr4: 52,568,978-53,225,011 USP46-DT, RASL11B, 9 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291206copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,685,685-58,104,722 , GRCh38.p12 chr4: 51,819,519-57,238,556 SRD5A3, DCUN1D4, 96 more genes
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 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