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 856

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5955101insertion1nstd209human GRCh38 chr1: 92,742,641-92,742,641 , GRCh37.p13 chr1: 93,208,198-93,208,198 EVI5
    nsv5953674insertion1nstd209human GRCh38 chr1: 92,669,547-92,669,547 , GRCh37.p13 chr1: 93,135,104-93,135,104 EVI5
    nsv5948727insertion1nstd209human GRCh38 chr1: 92,701,962-92,701,962 , GRCh37.p13 chr1: 93,167,519-93,167,519 EVI5
    nsv5885008copy number variation1nstd209human GRCh38 chr1: 92,722,357-92,727,552 , GRCh37.p13 chr1: 93,187,914-93,193,109 EVI5
    nsv5878953copy number variation1nstd209human GRCh38 chr1: 92,719,086-92,720,488 , GRCh37.p13 chr1: 93,184,643-93,186,045 EVI5
    nsv5875981copy number variation1nstd209human GRCh38 chr1: 92,689,223-92,689,754 , GRCh37.p13 chr1: 93,154,780-93,155,311 EVI5
    nsv5870215copy number variation1nstd209human GRCh38 chr1: 92,770,600-92,772,392 , GRCh37.p13 chr1: 93,236,157-93,237,949 EVI5
    nsv5830813copy number variation2nstd209human GRCh38 chr1: 92,770,508-92,771,986 , GRCh37.p13 chr1: 93,236,065-93,237,543 EVI5
    nsv5830811copy number variation1nstd209human GRCh38 chr1: 92,722,258-92,726,845 , GRCh37.p13 chr1: 93,187,815-93,192,402 EVI5
    nsv5830810copy number variation2nstd209human GRCh38 chr1: 92,719,104-92,720,521 , GRCh37.p13 chr1: 93,184,661-93,186,078 EVI5
    nsv5718019mobile element insertion2nstd211human GRCh38 chr1: 92,676,086-92,676,086 , GRCh37.p13 chr1: 93,141,643-93,141,643 EVI5
    nsv5691604mobile element insertion2nstd211human GRCh38 chr1: 92,598,969-92,598,969 , GRCh37.p13 chr1: 93,064,526-93,064,526 EVI5
    nsv5690420mobile element insertion1nstd211human GRCh38 chr1: 92,634,230-92,634,230 , GRCh37.p13 chr1: 93,099,787-93,099,787 EVI5
    nsv5688229mobile element insertion1nstd211human GRCh38 chr1: 92,638,267-92,638,267 , GRCh37.p13 chr1: 93,103,824-93,103,824 EVI5
    nsv5687586mobile element insertion2nstd211human GRCh38 chr1: 92,529,383-92,529,383 , GRCh37.p13 chr1: 92,994,940-92,994,940 EVI5
    nsv5686495mobile element insertion2nstd211human GRCh38 chr1: 92,693,551-92,693,551 , GRCh37.p13 chr1: 93,159,108-93,159,108 EVI5
    nsv5684314mobile element insertion2nstd211human GRCh38 chr1: 92,768,299-92,768,299 , GRCh37.p13 chr1: 93,233,856-93,233,856 EVI5
    nsv5679370mobile element insertion2nstd211human GRCh38 chr1: 92,701,973-92,701,973 , GRCh37.p13 chr1: 93,167,530-93,167,530 EVI5
    nsv5605768insertion1nstd207human GRCh38 chr1: 92,701,962-92,701,962 , GRCh37.p13 chr1: 93,167,519-93,167,519 EVI5
    nsv5574997copy number variation1nstd207human GRCh38 chr1: 92,719,086-92,720,488 , GRCh37.p13 chr1: 93,184,643-93,186,045 EVI5
    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