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 493

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5897178copy number variation1nstd209human GRCh38 chr4: 932,428-932,511 , GRCh37.p13 chr4: 926,216-926,299 GAK, TMEM175
    nsv5895284copy number variation1nstd209human GRCh38 chr4: 940,254-941,180 , GRCh37.p13 chr4: 934,042-934,968 TMEM175
    nsv5893160copy number variation1nstd209human GRCh38 chr4: 939,352-939,486 , GRCh37.p13 chr4: 933,140-933,274 TMEM175
    nsv5688526mobile element insertion2nstd211human GRCh38 chr4: 934,429-934,429 , GRCh37.p13 chr4: 928,217-928,217 TMEM175
    nsv5673651copy number variation1nstd102humanPathogenic GRCh37 chr4: 493,125-998,181 , GRCh38.p12 chr4: 499,336-1,004,393 ATP5ME, PDE6B, 19 more genes
    nsv5620817insertion1nstd207human GRCh38 chr4: 950,684-950,684 , GRCh37.p13 chr4: 944,472-944,472 TMEM175
    nsv5569538copy number variation1nstd207human GRCh38 chr4: 939,352-939,486 , GRCh37.p13 chr4: 933,140-933,274 TMEM175
    nsv5453510copy number variation1nstd206human GRCh38 chr4: 952,104-952,196 , GRCh37.p13 chr4: 945,892-945,984 TMEM175
    nsv5443866copy number variation1nstd206human GRCh38 chr4: 932,429-932,512 , GRCh37.p13 chr4: 926,217-926,300 GAK, TMEM175
    nsv5395325mobile element insertion1nstd206human GRCh38 chr4: 934,429-934,480 , GRCh37.p13 chr4: 928,217-928,268 TMEM175
    nsv5381775copy number variation1nstd102humanPathogenic GRCh37 chr4: 388,344-3,872,380 , GRCh38.p12 chr4: 394,555-3,870,653 RN7SL671P, HTT-AS, 96 more genes
    nsv5352443translocation1nstd200human GRCh38 chr4: 932,429-932,429 , GRCh38 chr4: 932,512-932,512 , GRCh37.p13 chr4: 926,300-926,300 , GRCh37.p13 chr4: 926,217-926,217 TMEM175, GAK
    nsv5303786copy number variation1nstd204human GRCh37.p13 chr4: 926,187-926,329 , GRCh38.p13 chr4: 932,399-932,541 GAK, TMEM175
    nsv5223166copy number variation1nstd204human GRCh38.p13 chr4: 637,201-1,087,400 , GRCh37.p13 chr4: 630,990-1,081,188 , SLC26A1, 19 more genes
    nsv5098682mobile element insertion1nstd203human GRCh38 chr4: 934,420-934,429 , GRCh37.p13 chr4: 928,208-928,217 TMEM175
    nsv5094628mobile element insertion1nstd203human GRCh38 chr4: 934,415-934,429 , GRCh37.p13 chr4: 928,203-928,217 TMEM175
    nsv5089962mobile element insertion1nstd203human GRCh38 chr4: 934,417-934,429 , GRCh37.p13 chr4: 928,205-928,217 TMEM175
    nsv5089830mobile element insertion1nstd203human GRCh38 chr4: 934,422-934,429 , GRCh37.p13 chr4: 928,210-928,217 TMEM175
    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