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 242

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5878440copy number variation1nstd209human GRCh38 chr1: 159,127,411-159,131,711 , GRCh37.p13 chr1: 159,097,201-159,101,501 AIM2
    nsv5872469copy number variation1nstd209human GRCh38 chr1: 159,096,295-159,098,487 , GRCh37.p13 chr1: 159,066,085-159,068,277 AIM2
    nsv5828260copy number variation1nstd209human GRCh38 chr1: 159,127,369-159,131,761 , GRCh37.p13 chr1: 159,097,159-159,101,551 AIM2
    nsv5828259copy number variation1nstd209human GRCh38 chr1: 159,067,835-159,068,834 , GRCh37.p13 chr1: 159,037,625-159,038,624 AIM2
    nsv5828056copy number variation1nstd209human GRCh38 chr1: 159,096,260-159,098,459 , GRCh37.p13 chr1: 159,066,050-159,068,249 AIM2
    nsv5725491mobile element insertion1nstd211human GRCh38 chr1: 159,066,526-159,066,526 , GRCh37.p13 chr1: 159,036,316-159,036,316 AIM2
    nsv5720733mobile element insertion1nstd211human GRCh38 chr1: 159,081,782-159,081,782 , GRCh37.p13 chr1: 159,051,572-159,051,572 RAD1P2, AIM2
    nsv5688956mobile element insertion1nstd211human GRCh38 chr1: 159,058,017-159,058,017 , GRCh37.p13 chr1: 159,027,807-159,027,807 , AIM2
    nsv5563915mobile element insertion1nstd206human GRCh38 chr1: 159,066,526-159,066,577 , GRCh37.p13 chr1: 159,036,316-159,036,367 AIM2
    nsv5563838mobile element insertion1nstd206human GRCh38 chr1: 159,081,782-159,081,833 , GRCh37.p13 chr1: 159,051,572-159,051,623 AIM2, RAD1P2
    nsv5429313copy number variation1nstd206human GRCh38 chr1: 159,127,414-159,131,712 , GRCh37.p13 chr1: 159,097,204-159,101,502 AIM2
    nsv5416817copy number variation1nstd206human GRCh38 chr1: 159,104,910-159,105,991 , GRCh37.p13 chr1: 159,074,700-159,075,781 AIM2
    nsv5416744copy number variation1nstd206human GRCh38 chr1: 159,096,301-159,098,488 , GRCh37.p13 chr1: 159,066,091-159,068,278 AIM2
    nsv5414526copy number variation1nstd206human GRCh38 chr1: 159,103,958-159,104,867 , GRCh37.p13 chr1: 159,073,748-159,074,657 AIM2
    nsv5398307mobile element insertion1nstd206human GRCh38 chr1: 159,058,017-159,058,068 , GRCh37.p13 chr1: 159,027,807-159,027,858 , AIM2
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5361484translocation1nstd200human GRCh38 chr1: 159,098,488-159,098,488 , GRCh38 chr1: 159,096,301-159,096,301 , GRCh37.p13 chr1: 159,068,278-159,068,278 , GRCh37.p13 chr1: 159,066,091-159,066,091 AIM2
    nsv5282614copy number variation1nstd204human GRCh38.p13 chr1: 159,096,301-159,098,488 , GRCh37.p13 chr1: 159,066,091-159,068,278 AIM2
    nsv5211742copy number variation1nstd204human GRCh38.p13 chr1: 159,092,501-159,098,500 , GRCh37.p13 chr1: 159,062,291-159,068,290 AIM2
    nsv5207381copy number variation1nstd204human GRCh38.p13 chr1: 159,096,260-159,098,509 , GRCh37.p13 chr1: 159,066,050-159,068,299 AIM2
    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