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 1264

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112800copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,889,977-21,463,189 , GRCh38.p12 chr22: 18,339,130-21,108,900 MIR4761, TUBA3FP, 124 more genes
    nsv6112793copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,889,693-21,465,485 , GRCh38.p12 chr22: 18,339,130-21,111,196 THAP7, LOC100129262, 125 more genes
    nsv6112781copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,841,374-21,465,101 , GRCh38.p12 chr22: 18,339,130-21,110,812 SEPTIN5, RNU6-225P, 125 more genes
    nsv6112779copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,889,571-21,464,697 , GRCh38.p12 chr22: 18,339,130-21,110,408 PRODH, MIR3618, 124 more genes
    nsv5980452copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,889,969-21,462,658 , GRCh38.p12 chr22: 18,339,130-21,108,369 LINC01637, BCRP7, 124 more genes
    nsv5976399inversion1nstd209human GRCh38 chr22: 17,577,704-20,098,016 , GRCh37.p13 chr22: 18,057,770-20,703,815 , ARVCF, 90 more genes
    nsv5695673mobile element insertion1nstd211human GRCh38 chr22: 18,881,342-18,881,342 , GRCh37.p13 chr22: 18,868,855-18,868,855 FAM230F
    nsv5673274copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,893,882-21,563,420 , GRCh38.p12 chr22: 18,339,130-21,209,131 UFD1-AS1, LOC100129254, 129 more genes
    nsv5673187copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr22: 18,900,688-21,351,637 , GRCh38.p12 chr22: 18,339,130-20,997,348 RN7SKP131, DGCR6, 114 more genes
    nsv5673185copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,893,882-21,571,027 , GRCh38.p12 chr22: 18,339,130-21,216,738 CCDC188, LOC107987325, 129 more genes
    nsv5671701insertion1nstd207human GRCh38 chr22: 18,892,006-18,892,006 , GRCh37.p13 chr22: 18,879,519-18,879,519 FAM230F
    nsv5670973insertion1nstd207human GRCh38 chr22: 18,873,028-18,873,028 , GRCh37.p13 chr22: 18,860,541-18,860,541 FAM230F
    nsv5670785inversion1nstd207human GRCh38 chr22: 18,746,351-21,188,291 , GRCh37.p13 chr22: 18,733,864-21,542,580 , ARVCF, 114 more genes
    nsv5670625insertion1nstd207human GRCh38 chr22: 18,893,330-18,893,330 , GRCh37.p13 chr22: 18,880,843-18,880,843 FAM230F
    nsv5670588insertion1nstd207human GRCh38 chr22: 18,873,037-18,873,037 , GRCh37.p13 chr22: 18,860,550-18,860,550 FAM230F
    nsv5669349insertion1nstd207human GRCh38 chr22: 18,873,307-18,873,307 , GRCh37.p13 chr22: 18,860,820-18,860,820 FAM230F
    nsv5668275insertion1nstd207human GRCh38 chr22: 18,891,352-18,891,352 , GRCh37.p13 chr22: 18,878,865-18,878,865 FAM230F
    nsv5667715insertion1nstd207human GRCh38 chr22: 18,892,062-18,892,062 , GRCh37.p13 chr22: 18,879,575-18,879,575 FAM230F
    nsv5667237insertion1nstd207human GRCh38 chr22: 18,892,291-18,892,291 , GRCh37.p13 chr22: 18,879,804-18,879,804 FAM230F
    nsv5666677insertion1nstd207human GRCh38 chr22: 18,891,984-18,891,984 , GRCh37.p13 chr22: 18,879,497-18,879,497 FAM230F
    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