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 120

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5560573sequence alteration1nstd206human GRCh38 chr8: 66,567,052-67,159,532 , GRCh37.p13 chr8: 67,479,287-68,071,767 PTTG3P, MCMDC2, 15 more genes
    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
    nsv4729605copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,744,375-68,387,850 , GRCh38.p12 chr8: 66,832,140-67,475,615 SNORD87, ARFGEF1-DT, 15 more genes
    nsv4729318copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,810,924-67,920,345 , GRCh38.p12 chr8: 66,898,689-67,008,110 MCMDC2, SNORD87, 4 more genes
    nsv4675786copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,718,713-68,020,835 , GRCh38.p12 chr8: 66,806,478-67,108,600 COPS5, SNHG6, 10 more genes
    nsv4675746copy number variation1nstd102humanLikely benign GRCh37 chr8: 67,828,205-68,074,172 , GRCh38.p12 chr8: 66,915,970-67,161,937 TCF24, COPS5, 8 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4455839copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,780,228-68,161,496 , GRCh38.p12 chr8: 66,867,993-67,249,261 LOC105375885, CSPP1, 10 more genes
    nsv4387546copy number variation1nstd173human GRCh37 chr8: 65,023,339-68,301,135 , GRCh38.p12 chr8: 64,110,782-67,388,900 , LOC105375885, 56 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4338988sequence alteration1nstd166human GRCh37.p13 chr8: 67,835,310-67,836,951 , GRCh38.p12 chr8: 66,923,075-66,924,716 MCMDC2, SNHG6
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv4169834copy number variation1nstd166human GRCh37.p13 chr8: 67,833,440-67,833,508 , GRCh38.p12 chr8: 66,921,205-66,921,273 SNHG6, MCMDC2, 1 more genes
    nsv4168641copy number variation1nstd166human GRCh37.p13 chr8: 67,837,708-67,837,810 , GRCh38.p12 chr8: 66,925,473-66,925,575 MCMDC2, SNHG6
    nsv4156721copy number variation1nstd166human GRCh37.p13 chr8: 67,836,757-67,838,118 , GRCh38.p12 chr8: 66,924,522-66,925,883 SNHG6, MCMDC2
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3923011copy number variation1nstd102humanPathogenic GRCh38 chr8: 66,171,669-93,505,509 , GRCh37 chr8: 67,083,904-94,517,737 , NCBI36 chr8: 67,246,458-94,586,913 CA3, HAUS1P3, 353 more genes
    nsv3922631copy number variation1nstd102humanPathogenic GRCh38 chr8: 61,691,800-82,537,696 , NCBI36 chr8: 62,766,913-83,612,486 , GRCh37 chr8: 62,604,359-83,449,931 NCOA2, LOC107986893, 284 more genes
    nsv3919282copy number variation1nstd102humanPathogenic GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824 MIR4662B, LOC101927845, 2104 more genes
    nsv3919200copy number variation1nstd102humanPathogenic GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639 LOC112268023, LOC105375925, 2103 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