U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 11127

  • The following terms were not found in dbVar: Chloropyridin, amine.
    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3130998copy number variation1nstd151human GRCh37 chr4: 93,225,805-93,511,442 , GRCh38.p12 chr4: 92,304,654-92,590,291 GRID2
    nsv3118857copy number variation1nstd151human GRCh37 chr4: 106,967,724-107,170,144 , GRCh38.p12 chr4: 106,046,567-106,248,987 TBCK
    nsv3137060copy number variation1nstd151human GRCh37 chr4: 126,237,564-126,412,928 , GRCh38.p12 chr4: 125,316,409-125,491,773 FAT4
    nsv3130543copy number variation1nstd151human GRCh37 chr4: 94,376,810-94,547,591 , GRCh38.p12 chr4: 93,455,659-93,626,440 GRID2
    nsv3119674copy number variation1nstd151human GRCh37 chr4: 162,680,560-162,841,809 , GRCh38.p12 chr4: 161,759,408-161,920,657 FSTL5
    nsv3128209copy number variation1nstd151human GRCh37 chr4: 151,656,407-151,789,020 , GRCh38.p12 chr4: 150,735,255-150,867,868 LRBA
    nsv3137112copy number variation1nstd151human GRCh37 chr4: 95,376,437-95,507,600 , GRCh38.p12 chr4: 94,455,286-94,586,449 PDLIM5
    nsv3123858copy number variation1nstd151human GRCh37 chr4: 151,719,230-151,850,222 , GRCh38.p12 chr4: 150,798,078-150,929,070 LRBA
    nsv3125888copy number variation1nstd151human GRCh37 chr4: 104,510,836-104,640,837 , GRCh38.p12 chr4: 103,589,679-103,719,680 TACR3
    nsv3119351copy number variation1nstd151human GRCh37 chr4: 89,708,901-89,827,618 , GRCh38.p12 chr4: 88,787,750-88,906,467 FAM13A
    nsv3122208copy number variation3nstd151human GRCh37 chr4: 89,711,734-89,827,618 , GRCh38.p12 chr4: 88,790,583-88,906,467 FAM13A
    nsv3125135copy number variation1nstd151human GRCh37 chr4: 36,115,789-36,231,113 , GRCh38.p12 chr4: 36,114,167-36,229,491 ARAP2
    nsv3137845copy number variation1nstd151human GRCh37 chr4: 151,738,273-151,850,222 , GRCh38.p12 chr4: 150,817,121-150,929,070 LRBA
    nsv3120930copy number variation1nstd151human GRCh37 chr4: 186,168,508-186,278,896 , GRCh38.p12 chr4: 185,247,354-185,357,742 SNX25
    nsv3121665copy number variation1nstd151human GRCh37 chr4: 107,133,904-107,230,122 , GRCh38.p12 chr4: 106,212,747-106,308,965 TBCK
    nsv3130076copy number variation1nstd151human GRCh37 chr4: 162,306,896-162,402,326 , GRCh38.p12 chr4: 161,385,744-161,481,174 FSTL5
    nsv3121702copy number variation1nstd151human GRCh37 chr4: 23,797,442-23,891,585 , GRCh38.p12 chr4: 23,795,819-23,889,962 PPARGC1A
    nsv3132004copy number variation2nstd151human GRCh37 chr4: 23,803,844-23,891,585 , GRCh38.p12 chr4: 23,802,221-23,889,962 PPARGC1A
    nsv3130168copy number variation1nstd151human GRCh37 chr4: 22,389,325-22,475,471 , GRCh38.p12 chr4: 22,387,702-22,473,848 ADGRA3
    nsv3131580copy number variation5nstd151human GRCh37 chr4: 89,744,124-89,827,618 , GRCh38.p12 chr4: 88,822,973-88,906,467 FAM13A
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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