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 162

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052940inversion1nstd229human GRCh38 chr4: 73,455,263-76,320,440 , GRCh37.p13 chr4: 74,320,980-77,241,593 , RASSF6, 65 more genes
    nsv7045939inversion1nstd229human GRCh38 chr4: 69,867,306-75,844,103 , GRCh37.p13 chr4: 70,733,024-76,765,256 , PF4V1, 99 more genes
    nsv7040415inversion1nstd229human GRCh38 chr4: 72,183,424-80,893,316 , GRCh37.p13 chr4: 73,049,141-81,814,470 , KPNA2P1, 148 more genes
    nsv6756994copy number variation1nstd229human GRCh38 chr4: 73,978,039-75,072,537 , GRCh37.p13 chr4: 74,843,756-75,997,747 LOC105377280, LOC105377277, 22 more genes
    nsv6752725copy number variation1nstd229human GRCh38 chr4: 74,452,030-74,462,167 , GRCh37.p13 chr4: 75,317,747-75,327,884 AREG
    nsv6750657copy number variation1nstd229human GRCh38 chr4: 74,199,394-75,056,456 , GRCh37.p13 chr4: 75,065,111-75,981,666 MTHFD2L, HSPE1P23, 12 more genes
    nsv6749244copy number variation1nstd229human GRCh38 chr4: 71,830,854-79,510,197 , GRCh37.p13 chr4: 72,696,571-80,431,351 , COX18, 134 more genes
    nsv6749090copy number variation1nstd229human GRCh38 chr4: 74,442,501-74,450,900 , GRCh37.p13 chr4: 75,308,218-75,316,617 AREG
    nsv6738651copy number variation1nstd229human GRCh38 chr4: 74,168,885-74,760,317 , GRCh37.p13 chr4: 75,034,602-75,382,209 BTC, EREG, 5 more genes
    nsv6636541copy number variation1nstd102humanUncertain significance GRCh37 chr4: 75,244,024-75,866,729 , GRCh38.p12 chr4: 74,378,307-74,941,519 HSPE1P23, LOC105377282, 7 more genes
    nsv6565136inversion1nstd223human GRCh38 chr4: 74,413,523-83,001,891 , GRCh37.p13 chr4: 75,279,240-83,923,044 RNU6-615P, SHROOM3, 144 more genes
    nsv6391982copy number variation1nstd223human GRCh38 chr4: 74,452,030-74,462,167 , GRCh37.p13 chr4: 75,317,747-75,327,884 AREG
    nsv6391428copy number variation1nstd223human GRCh38 chr4: 74,450,910-74,639,938 , GRCh37.p13 chr4|NW_003571035.1: 1-123,446 , GRCh37.p13 chr4: 75,382,210-75,565,154 AREG, LOC107986229
    nsv6387290copy number variation1nstd223human GRCh38 chr4: 74,189,282-74,801,973 , GRCh37.p13 chr4: 75,054,999-75,727,183 EREG, EPGN, 5 more genes
    nsv6314916copy number variation1nstd102humanPathogenic GRCh38 chr4: 67,833,055-82,716,065 , GRCh37.p13 chr4: 68,698,773-83,637,218 MICOS10P4, SULT1B1, 274 more genes
    nsv6313715copy number variation1nstd102humanPathogenic GRCh37 chr4: 73,055,313-80,083,154 , GRCh38.p12 chr4: 72,189,596-79,162,000 CCNG2, FTLP9, 129 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6135609copy number variation1nstd213human GRCh37 chr4: 75,050,000-75,430,001 , GRCh38.p12 chr4: 74,184,283-74,561,653 AREG, EREG, 4 more genes
    nsv6135608copy number variation1nstd213human GRCh37 chr4: 74,850,000-75,530,001 , GRCh38.p12 chr4: 73,984,283-74,604,784 AREG, EREG, 13 more genes
    nsv6135360copy number variation1nstd213human GRCh37 chr4: 74,880,000-75,500,001 , GRCh38.p12 chr4: 74,014,283-74,574,820 AREG, EREG, 10 more genes
    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