U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 99

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673865copy number variation1nstd102humanPathogenic GRCh37 chr8: 145,738,945-145,743,168 , GRCh38.p12 chr8: 144,513,561-144,517,784 LRRC14, RECQL4
    nsv6312817copy number variation1nstd102humanPathogenic GRCh37 chr8: 145,739,302-145,743,168 , GRCh38.p12 chr8: 144,513,918-144,517,784 LRRC14, RECQL4
    nsv6312816copy number variation1nstd102humanPathogenic GRCh37 chr8: 145,738,234-145,741,987 , GRCh38.p12 chr8: 144,512,851-144,516,603 LRRC14, RECQL4
    nsv4683161copy number variation1nstd102humanPathogenic GRCh37 chr8: 145,740,310-145,743,178 , GRCh38.p12 chr8: 144,514,926-144,517,794 LRRC14, RECQL4
    nsv4681887copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 145,738,591-145,742,902 , GRCh38.p12 chr8: 144,513,208-144,517,518 LRRC14, RECQL4
    nsv5564447copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,742,505-145,742,567 , GRCh38 chr8: 144,517,121-144,517,183 LRRC14, RECQL4
    nsv5381554copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,737,517-145,743,168 , GRCh38.p12 chr8: 144,512,134-144,517,784 LRRC14, RECQL4
    nsv7098168copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,742,424-145,743,168 , GRCh38.p12 chr8: 144,517,040-144,517,784 LRRC14, RECQL4
    nsv3872276copy number variation1nstd102humanUncertain significance GRCh38 chr8: 144,517,592-144,517,794 , GRCh37 chr8: 145,742,976-145,743,178 LRRC14, RECQL4
    nsv5564498copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,742,976-145,743,168 , GRCh38.p12 chr8: 144,517,592-144,517,784 LRRC14, RECQL4
    nsv4681906copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr8: 145,736,814-145,743,168 , GRCh38.p12 chr8: 144,511,431-144,517,784 LRRC14, RECQL4, 1 more genes
    nsv6312711copy number variation1nstd102humanPathogenic GRCh37 chr8: 145,742,531-145,747,630 , GRCh38.p12 chr8: 144,517,147-144,522,246 LRRC14, RECQL4, 1 more genes
    nsv4450060copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,736,804-145,743,178 , GRCh38.p12 chr8: 144,511,421-144,517,794 LRRC14, MFSD3, 1 more genes
    nsv3879118copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,736,809-145,743,174 , GRCh38.p12 chr8: 144,511,426-144,517,790 LRRC14, RECQL4, 1 more genes
    nsv5564448copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,736,814-145,742,902 , GRCh38.p12 chr8: 144,511,431-144,517,518 LRRC14, RECQL4, 1 more genes
    nsv7097655copy number variation1nstd102humanPathogenic GRCh37 chr8: 145,741,748-145,958,266 , GRCh38.p12 chr8: 144,516,364-144,732,881 LRRC14, RECQL4, 5 more genes
    nsv3915173copy number variation1nstd102humanPathogenic NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636 LRRC14, RN7SL474P, 2109 more genes
    nsv3901821copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028 LRRC14, TBC1D31, 2109 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LRRC14, LOC101929488, 2105 more genes
    nsv3916777copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575 LRRC14, RPL5P22, 2105 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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