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 397

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968895inversion1nstd209human GRCh38 chr1: 86,344,334-89,254,011 , GRCh37.p13 chr1: 86,810,017-89,719,694 , CLCA1, 53 more genes
    nsv5884423copy number variation1nstd209human GRCh38 chr1: 86,615,915-86,636,116 , GRCh37.p13 chr1: 87,081,598-87,101,799 CLCA4-AS1, CLCA3P
    nsv5873028copy number variation1nstd209human GRCh38 chr1: 86,631,307-86,632,694 , GRCh37.p13 chr1: 87,096,990-87,098,377 CLCA4-AS1, CLCA3P
    nsv5869850copy number variation1nstd209human GRCh38 chr1: 86,663,226-86,673,646 , GRCh37.p13 chr1: 87,128,909-87,139,329 CLCA4-AS1
    nsv5869037copy number variation1nstd209human GRCh38 chr1: 86,562,528-86,573,602 , GRCh37.p13 chr1: 87,028,211-87,039,285 CLCA4, CLCA4-AS1
    nsv5830826copy number variation1nstd209human GRCh38 chr1: 86,631,254-86,632,754 , GRCh37.p13 chr1: 87,096,937-87,098,437 CLCA3P, CLCA4-AS1
    nsv5830782copy number variation1nstd209human GRCh38 chr1: 86,631,255-86,634,291 , GRCh37.p13 chr1: 87,096,938-87,099,974 CLCA4-AS1, CLCA3P
    nsv5830781copy number variation2nstd209human GRCh38 chr1: 86,627,779-86,630,999 , GRCh37.p13 chr1: 87,093,462-87,096,682 CLCA4-AS1
    nsv5830780copy number variation1nstd209human GRCh38 chr1: 86,611,802-86,615,819 , GRCh37.p13 chr1: 87,077,485-87,081,502 CLCA4-AS1
    nsv5830779copy number variation1nstd209human GRCh38 chr1: 86,610,368-86,630,530 , GRCh37.p13 chr1: 87,076,051-87,096,213 CLCA4-AS1
    nsv5830778copy number variation1nstd209human GRCh38 chr1: 86,563,280-86,573,342 , GRCh37.p13 chr1: 87,028,963-87,039,025 CLCA4, CLCA4-AS1
    nsv5830518copy number variation1nstd209human GRCh38 chr1: 86,631,256-86,636,136 , GRCh37.p13 chr1: 87,096,939-87,101,819 CLCA3P, CLCA4-AS1
    nsv5721071mobile element insertion1nstd211human GRCh38 chr1: 86,689,673-86,689,673 , GRCh37.p13 chr1: 87,155,356-87,155,356 CLCA4-AS1
    nsv5682476mobile element insertion1nstd211human GRCh38 chr1: 86,590,531-86,590,531 , GRCh37.p13 chr1: 87,056,214-87,056,214 CLCA4-AS1
    nsv5674896mobile element insertion2nstd211human GRCh38 chr1: 86,569,501-86,569,501 , GRCh37.p13 chr1: 87,035,184-87,035,184 CLCA4, CLCA4-AS1
    nsv5620439insertion1nstd207human GRCh38 chr1: 86,589,969-86,589,969 , GRCh37.p13 chr1: 87,055,652-87,055,652 CLCA4-AS1
    nsv5617721insertion1nstd207human GRCh38 chr1: 86,634,068-86,634,068 , GRCh37.p13 chr1: 87,099,751-87,099,751 CLCA4-AS1, CLCA3P
    nsv5607946insertion1nstd207human GRCh38 chr1: 86,674,895-86,674,895 , GRCh37.p13 chr1: 87,140,578-87,140,578 CLCA4-AS1
    nsv5583512copy number variation1nstd207human GRCh38 chr1: 86,634,078-86,636,115 , GRCh37.p13 chr1: 87,099,761-87,101,798 CLCA4-AS1, CLCA3P
    nsv5576807copy number variation1nstd207human GRCh38 chr1: 86,610,328-86,610,995 , GRCh37.p13 chr1: 87,076,011-87,076,678 CLCA4-AS1
    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