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 1200

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147511insertion1nstd232human GRCh37.p13 chr4: 66,469,801-66,469,801 , GRCh38.p12 chr4: 65,604,083-65,604,083 EPHA5
    nsv7054721inversion1nstd229human GRCh38 chr4: 65,506,976-65,520,511 , GRCh37.p13 chr4: 66,372,694-66,386,229 EPHA5
    nsv7042248inversion1nstd229human GRCh38 chr4: 65,412,821-65,415,159 , GRCh37.p13 chr4: 66,278,539-66,280,877 EPHA5
    nsv6757735copy number variation1nstd229human GRCh38 chr4: 62,015,862-66,463,521 , GRCh37.p13 chr4: 62,881,580-67,329,239 EXOC5P1, MTCO3P28, 37 more genes
    nsv6756776copy number variation1nstd229human GRCh38 chr4: 65,416,701-65,419,600 , GRCh37.p13 chr4: 66,282,419-66,285,318 EPHA5
    nsv6756547copy number variation1nstd229human GRCh38 chr4: 65,580,741-65,581,175 , GRCh37.p13 chr4: 66,446,459-66,446,893 EPHA5
    nsv6756221copy number variation1nstd229human GRCh38 chr4: 65,582,672-65,677,910 , GRCh37.p13 chr4: 66,448,390-66,543,628 EPHA5-AS1, EPHA5
    nsv6755896copy number variation1nstd229human GRCh38 chr4: 65,446,334-65,450,546 , GRCh37.p13 chr4: 66,312,052-66,316,264 EPHA5
    nsv6755584copy number variation1nstd229human GRCh38 chr4: 65,506,301-65,506,700 , GRCh37.p13 chr4: 66,372,019-66,372,418 EPHA5
    nsv6754788copy number variation1nstd229human GRCh38 chr4: 65,297,846-65,321,502 , GRCh37.p13 chr4: 66,163,564-66,187,220 EPHA5
    nsv6753199copy number variation1nstd229human GRCh38 chr4: 65,454,109-65,456,456 , GRCh37.p13 chr4: 66,319,827-66,322,174 EPHA5
    nsv6752360copy number variation1nstd229human GRCh38 chr4: 65,462,749-65,480,503 , GRCh37.p13 chr4: 66,328,467-66,346,221 EPHA5
    nsv6751910copy number variation1nstd229human GRCh38 chr4: 65,462,824-65,469,671 , GRCh37.p13 chr4: 66,328,542-66,335,389 EPHA5
    nsv6751213copy number variation1nstd229human GRCh38 chr4: 65,654,367-65,655,124 , GRCh37.p13 chr4: 66,520,085-66,520,842 EPHA5
    nsv6749999copy number variation1nstd229human GRCh38 chr4: 65,416,165-65,416,861 , GRCh37.p13 chr4: 66,281,883-66,282,579 EPHA5
    nsv6749575copy number variation1nstd229human GRCh38 chr4: 65,650,823-65,659,964 , GRCh37.p13 chr4: 66,516,541-66,525,682 EPHA5
    nsv6748959copy number variation1nstd229human GRCh38 chr4: 65,557,701-65,559,900 , GRCh37.p13 chr4: 66,423,419-66,425,618 EPHA5
    nsv6748663copy number variation1nstd229human GRCh38 chr4: 65,634,034-65,634,106 , GRCh37.p13 chr4: 66,499,752-66,499,824 EPHA5
    nsv6746810copy number variation1nstd229human GRCh38 chr4: 65,432,196-65,442,552 , GRCh37.p13 chr4: 66,297,914-66,308,270 EPHA5
    nsv6745457copy number variation1nstd229human GRCh38 chr4: 65,451,502-65,458,156 , GRCh37.p13 chr4: 66,317,220-66,323,874 EPHA5
    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