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 154

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7060811inversion1nstd229human GRCh38 chr8: 66,867,173-66,996,888 , GRCh37.p13 chr8: 67,779,408-67,909,123 PPP1R42, SNHG6, 4 more genes
    nsv6848593copy number variation1nstd229human GRCh38 chr8: 66,853,627-67,142,119 , GRCh37.p13 chr8: 67,765,862-68,054,354 SNHG6, C8orf44-SGK3, 10 more genes
    nsv6839562copy number variation1nstd229human GRCh38 chr8: 66,955,837-67,206,457 , GRCh37.p13 chr8: 67,868,072-68,118,692 ARFGEF1, CSPP1, 7 more genes
    nsv6636616copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,642,641-68,406,704 , GRCh38.p12 chr8: 66,730,406-67,494,469 C8orf44-SGK3, LOC105375885, 16 more genes
    nsv6636205copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,261,729-68,676,568 , GRCh38.p12 chr8: 66,349,494-67,764,333 C8orf44-SGK3, SNHG6, 36 more genes
    nsv6633020copy number variation1nstd224human GRCh37 chr8: 67,734,618-68,102,996 , GRCh38.p12 chr8: 66,822,383-67,190,761 MCMDC2, TCF24, 12 more genes
    nsv6632899copy number variation1nstd224human GRCh37 chr8: 67,786,385-68,163,686 , GRCh38.p12 chr8: 66,874,150-67,251,451 COPS5, SNHG6, 10 more genes
    nsv6574006inversion1nstd223human GRCh38 chr8: 66,944,947-66,945,319 , GRCh37.p13 chr8: 67,857,182-67,857,554 TCF24
    nsv6433181copy number variation1nstd223human GRCh38 chr8: 66,961,201-66,963,400 , GRCh37.p13 chr8: 67,873,436-67,875,635 PPP1R42, TCF24
    nsv6424371copy number variation1nstd223human GRCh38 chr8: 66,791,690-67,039,259 , GRCh37.p13 chr8: 67,703,925-67,951,494 PPP1R42, LOC100288001, 7 more genes
    nsv6290731copy number variation1nstd102humanPathogenic GRCh37 chr8: 66,045,954-69,807,260 , GRCh38.p12 chr8: 65,133,719-68,895,025 LINC00967, LOC107986950, 64 more genes
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv6136068copy number variation1nstd213human GRCh37 chr8: 67,390,000-69,660,001 , GRCh38.p12 chr8: 66,477,765-68,747,766 ARFGEF1, SGK3, 41 more genes
    nsv5712900mobile element insertion1nstd211human GRCh38 chr8: 66,947,638-66,947,638 , GRCh37.p13 chr8: 67,859,873-67,859,873 TCF24
    nsv5560573sequence alteration1nstd206human GRCh38 chr8: 66,567,052-67,159,532 , GRCh37.p13 chr8: 67,479,287-68,071,767 PTTG3P, MCMDC2, 15 more genes
    nsv5479923copy number variation1nstd206human GRCh38 chr8: 66,948,295-66,948,674 , GRCh37.p13 chr8: 67,860,530-67,860,909 TCF24
    nsv5408855mobile element insertion1nstd206human GRCh38 chr8: 66,947,638-66,947,689 , GRCh37.p13 chr8: 67,859,873-67,859,924 TCF24
    nsv5381480copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,786,376-68,165,857 , GRCh38.p12 chr8: 66,874,141-67,253,622 NPM1P44, LOC100288001, 10 more genes
    nsv5305794copy number variation1nstd204human GRCh38.p13 chr8: 66,931,202-66,956,273 , GRCh37.p13 chr8: 67,843,437-67,868,508 TCF24
    nsv5246833copy number variation1nstd204human GRCh38.p13 chr8: 66,930,291-66,956,472 , GRCh37.p13 chr8: 67,842,526-67,868,707 TCF24
    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