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 491

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv4006778copy number variation1estd231human GRCh37 chr4: 89,522,908-89,523,223 , GRCh38.p12 chr4: 88,601,757-88,602,072 HERC3
    nsv6756112copy number variation1nstd229human GRCh38 chr4: 88,536,757-88,543,662 , GRCh37.p13 chr4: 89,457,908-89,464,813 HERC3
    nsv6742740copy number variation1nstd229human GRCh38 chr4: 88,620,941-88,626,418 , GRCh37.p13 chr4: 89,542,092-89,547,569 HERC3
    nsv6754996copy number variation1nstd229human GRCh38 chr4: 88,630,103-88,633,652 , GRCh37.p13 chr4: 89,551,254-89,554,803 HERC3
    nsv6740853copy number variation1nstd229human GRCh38 chr4: 88,601,773-88,602,072 , GRCh37.p13 chr4: 89,522,924-89,523,223 HERC3
    nsv6741085copy number variation1nstd229human GRCh38 chr4: 88,698,573-88,698,612 , GRCh37.p13 chr4: 89,619,724-89,619,763 HERC3
    nsv6382620copy number variation1nstd223human GRCh38 chr4: 88,669,536-88,678,089 , GRCh37.p13 chr4: 89,590,687-89,599,240 HERC3
    nsv6384340copy number variation1nstd223human GRCh38 chr4: 88,564,512-88,567,705 , GRCh37.p13 chr4: 89,485,663-89,488,856 HERC3
    nsv6377214copy number variation1nstd223human GRCh38 chr4: 88,700,588-88,701,467 , GRCh37.p13 chr4: 89,621,739-89,622,618 HERC3
    nsv6390421copy number variation1nstd223human GRCh38 chr4: 88,667,548-88,668,198 , GRCh37.p13 chr4: 89,588,699-89,589,349 HERC3
    nsv6391969copy number variation1nstd223human GRCh38 chr4: 88,649,651-88,650,186 , GRCh37.p13 chr4: 89,570,802-89,571,337 HERC3
    nsv6388578copy number variation1nstd223human GRCh38 chr4: 88,688,134-88,688,502 , GRCh37.p13 chr4: 89,609,285-89,609,653 HERC3
    nsv6390726copy number variation1nstd223human GRCh38 chr4: 88,601,757-88,602,072 , GRCh37.p13 chr4: 89,522,908-89,523,223 HERC3
    nsv5458084copy number variation1nstd206human GRCh38 chr4: 88,601,614-88,602,403 , GRCh37.p13 chr4: 89,522,765-89,523,554 HERC3
    nsv5459759copy number variation1nstd206human GRCh38 chr4: 88,558,550-88,559,086 , GRCh37.p13 chr4: 89,479,701-89,480,237 HERC3
    nsv5456488copy number variation1nstd206human GRCh38 chr4: 88,601,773-88,602,072 , GRCh37.p13 chr4: 89,522,924-89,523,223 HERC3
    nsv5469351copy number variation1nstd206human GRCh38 chr4: 88,539,274-88,539,369 , GRCh37.p13 chr4: 89,460,425-89,460,520 HERC3
    nsv4640039copy number variation1nstd186human GRCh37 chr4: 89,522,789-89,523,223 , GRCh38.p12 chr4: 88,601,638-88,602,072 HERC3
    nsv4643381mobile element deletion1nstd186human GRCh37 chr4: 89,522,909-89,523,223 , GRCh38.p12 chr4: 88,601,758-88,602,072 HERC3
    nsv5382001mobile element deletion2nstd186human GRCh37 chr4: 89,522,924-89,523,223 , GRCh38.p12 chr4: 88,601,773-88,602,072 HERC3
    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