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 183

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6648551copy number variation1nstd229human GRCh38 chr1: 29,149,228-29,154,693 , GRCh37.p13 chr1: 29,475,740-29,481,205 SRSF4
    nsv6647913copy number variation1nstd229human GRCh38 chr1: 29,177,426-29,180,494 , GRCh37.p13 chr1: 29,503,938-29,507,006 SRSF4
    nsv6316070copy number variation1nstd223human GRCh38 chr1: 29,177,426-29,180,495 , GRCh37.p13 chr1: 29,503,938-29,507,007 SRSF4
    nsv6323490copy number variation1nstd223human GRCh38 chr1: 29,145,028-29,147,527 , GRCh37.p13 chr1: 29,471,540-29,474,039 SRSF4
    nsv6330360copy number variation1nstd223human GRCh38 chr1: 29,153,848-29,154,442 , GRCh37.p13 chr1: 29,480,360-29,480,954 SRSF4
    nsv5874268copy number variation1nstd209human GRCh38 chr1: 29,143,738-29,147,639 , GRCh37.p13 chr1: 29,470,250-29,474,151 SRSF4
    nsv4772863copy number variation1nstd200human GRCh37 chr1: 29,470,269-29,474,136 , GRCh38.p12 chr1: 29,143,757-29,147,624 SRSF4
    nsv5883359copy number variation1nstd209human GRCh38 chr1: 29,175,147-29,175,420 , GRCh37.p13 chr1: 29,501,659-29,501,932 SRSF4
    nsv4042854copy number variation1nstd166human GRCh37.p13 chr1: 29,503,938-29,507,007 , GRCh38.p12 chr1: 29,177,426-29,180,495 SRSF4
    nsv4037163copy number variation1nstd166human GRCh37.p13 chr1: 29,480,398-29,480,954 , GRCh38.p12 chr1: 29,153,886-29,154,442 SRSF4
    nsv4594461copy number variation1nstd183human GRCh37 chr1: 29,486,011-29,486,852 , GRCh38.p12 chr1: 29,159,499-29,160,340 SRSF4
    nsv1173073copy number variation226nstd112Neandertal, Denisova hominin, human GRCh37 chr1: 29,469,579-29,474,646 , GRCh38.p12 chr1: 29,143,067-29,148,134 SRSF4
    esv2991187copy number variation1estd209human GRCh37 chr1: 29,508,876-29,508,881 , GRCh38.p12 chr1: 29,182,364-29,182,369 SRSF4
    esv2991183copy number variation1estd209human GRCh37 chr1: 29,473,544-29,473,547 , GRCh38.p12 chr1: 29,147,032-29,147,035 SRSF4
    esv2991185copy number variation1estd209human GRCh37 chr1: 29,494,703-29,494,705 , GRCh38.p12 chr1: 29,168,191-29,168,193 SRSF4
    esv2991186copy number variation1estd209human GRCh37 chr1: 29,500,724-29,500,725 , GRCh38.p12 chr1: 29,174,212-29,174,213 SRSF4
    esv2991184copy number variation1estd209human GRCh37 chr1: 29,487,904-29,487,905 , GRCh38.p12 chr1: 29,161,392-29,161,393 SRSF4
    esv2568923copy number variation1estd197human NCBI36 chr1: 29,345,474-29,345,475 , GRCh37.p13 chr1: 29,472,887-29,472,888 , GRCh38.p12 chr1: 29,146,375-29,146,376 SRSF4
    esv2389563copy number variation1estd194human NCBI36 chr1: 29,375,572-29,375,579 , GRCh37.p13 chr1: 29,502,985-29,502,992 , GRCh38.p12 chr1: 29,176,473-29,176,480 SRSF4
    esv2222313copy number variation1estd194human NCBI36 chr1: 29,372,228-29,372,230 , GRCh37.p13 chr1: 29,499,641-29,499,643 , GRCh38.p12 chr1: 29,173,129-29,173,131 SRSF4
    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