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 366

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940105copy number variation1nstd209human GRCh38 chr19: 1,243,036-1,243,610 , GRCh37.p13 chr19: 1,243,035-1,243,609 ATP5F1D
    esv3218222copy number variation1estd209human GRCh37 chr19: 1,240,768-1,240,772 , GRCh38.p12 chr19: 1,240,769-1,240,773 ATP5F1D
    esv3218221copy number variation1estd209human GRCh37 chr19: 1,240,756-1,240,759 , GRCh38.p12 chr19: 1,240,757-1,240,760 ATP5F1D
    esv2319936copy number variation1estd194human NCBI36 chr19: 1,192,405-1,192,406 , GRCh37.p13 chr19: 1,241,405-1,241,406 , GRCh38.p12 chr19: 1,241,406-1,241,407 ATP5F1D
    esv2267693copy number variation1estd194human NCBI36 chr19: 1,192,390-1,192,391 , GRCh37.p13 chr19: 1,241,390-1,241,391 , GRCh38.p12 chr19: 1,241,391-1,241,392 ATP5F1D
    esv1773646copy number variation1estd22human NCBI36 chr19: 1,191,771-1,191,774 , GRCh37.p13 chr19: 1,240,771-1,240,774 , GRCh38.p12 chr19: 1,240,772-1,240,775 ATP5F1D
    esv1667548copy number variation1estd22human NCBI36 chr19: 1,192,403-1,192,404 , GRCh37.p13 chr19: 1,241,403-1,241,404 , GRCh38.p12 chr19: 1,241,404-1,241,405 ATP5F1D
    nsv5285835copy number variation1nstd204human GRCh38.p13 chr19: 1,241,050-1,242,449 , GRCh37.p13 chr19: 1,241,049-1,242,448 ATP5F1D
    nsv5292756copy number variation1nstd204human GRCh38.p13 chr19: 1,240,550-1,241,649 , GRCh37.p13 chr19: 1,240,549-1,241,648 ATP5F1D
    nsv7095265copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,241,850-1,244,436 , GRCh38.p12 chr19: 1,241,851-1,244,437 ATP5F1D, LOC102723811
    nsv7000141copy number variation1nstd229human GRCh38 chr19: 1,244,246-1,244,403 , GRCh37.p13 chr19: 1,244,245-1,244,402 ATP5F1D, LOC102723811
    nsv4258123copy number variation1nstd166human GRCh37.p13 chr19: 1,244,245-1,244,402 , GRCh38.p12 chr19: 1,244,246-1,244,403 LOC102723811, ATP5F1D
    nsv6145904copy number variation1nstd206human GRCh38 chr19: 1,238,000-1,244,000 , GRCh37.p13 chr19: 1,237,999-1,243,999 CBARP, ATP5F1D
    nsv6306890copy number variation1nstd186human GRCh37 chr19: 1,237,999-1,243,999 , GRCh38.p12 chr19: 1,238,000-1,244,000 ATP5F1D, CBARP
    nsv5287384copy number variation1nstd204human GRCh38.p13 chr19: 1,233,348-1,242,649 , GRCh37.p13 chr19: 1,233,347-1,242,648 ATP5F1D, CBARP
    esv3770942complex chromosomal rearrangement1estd192human GRCh37 chr19: 1,243,721-1,243,741 , GRCh37 chr6: 30,831,041-30,831,061 , GRCh38.p12 chr6: 30,863,264-30,863,284 , GRCh38.p12 chr19: 1,243,722-1,243,742 RN7SKP186, ATP5F1D
    nsv3893093copy number variation1nstd102humanBenign GRCh37 chr19: 1,241,594-1,250,885 , GRCh38.p12 chr19: 1,241,595-1,250,886 ATP5F1D, LOC102723811, 1 more genes
    nsv3897821copy number variation1nstd102humanBenign GRCh37 chr19: 1,242,574-1,250,885 , GRCh38.p12 chr19: 1,242,575-1,250,886 LOC102723811, MIDN, 1 more genes
    nsv3891796copy number variation1nstd102humanBenign GRCh37 chr19: 1,199,815-1,244,170 , GRCh38.p12 chr19: 1,199,816-1,244,171 ATP5F1D, HMGB2P1, 2 more genes
    nsv3900174copy number variation1nstd102humanBenign GRCh37 chr19: 1,218,523-1,257,027 , GRCh38.p12 chr19: 1,218,524-1,257,028 STK11, LOC102723811, 3 more genes
    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