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 699

    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
    nsv6112789copy number variation1nstd102humanPathogenic GRCh37 chr22: 20,730,996-21,465,342 , GRCh38.p12 chr22: 20,376,706-21,111,053 IGLL4P, CRKL, 39 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
    nsv5980456copy number variation1nstd102humanUncertain significance GRCh37 chr22: 20,737,912-21,465,659 , GRCh38.p12 chr22: 20,383,622-21,111,370 KRT18P5, SLC9A3P2, 39 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
    nsv5967784inversion1nstd209human GRCh38 chr22: 20,337,735-21,327,040 , GRCh37.p13 chr22: 20,325,258-21,681,329 , CRKL, 49 more genes
    nsv5964986copy number variation1nstd209human GRCh38 chr22: 20,860,838-20,860,910 , GRCh37.p13 chr22: 21,215,126-21,215,198 SNAP29
    nsv5963759copy number variation1nstd209human GRCh38 chr22: 20,865,173-20,868,782 , GRCh37.p13 chr22: 21,219,461-21,223,070 SNAP29
    nsv5954847copy number variation1nstd209human GRCh38 chr22: 20,879,263-20,879,494 , GRCh37.p13 chr22: 21,233,551-21,233,782 SNAP29
    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
    nsv5670785inversion1nstd207human GRCh38 chr22: 18,746,351-21,188,291 , GRCh37.p13 chr22: 18,733,864-21,542,580 , ARVCF, 114 more genes
    nsv5548031copy number variation1nstd206human GRCh38 chr22: 20,875,882-20,879,029 , GRCh37.p13 chr22: 21,230,170-21,233,317 SNAP29
    nsv5547366copy number variation1nstd206human GRCh38 chr22: 20,875,594-20,875,713 , GRCh37.p13 chr22: 21,229,882-21,230,001 SNAP29
    nsv5546016copy number variation1nstd206human GRCh38 chr22: 20,689,282-21,312,400 , GRCh37.p13 chr22: 21,043,570-21,666,689 , BCRP2, 30 more genes
    nsv5543736copy number variation1nstd206human GRCh38 chr22: 20,860,838-20,860,932 , GRCh37.p13 chr22: 21,215,126-21,215,220 SNAP29
    nsv5542624copy number variation1nstd206human GRCh38 chr22: 20,874,083-20,876,006 , GRCh37.p13 chr22: 21,228,371-21,230,294 SNAP29
    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