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 151

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5538176copy number variation1nstd206human GRCh38 chr22: 30,322,815-30,323,124 , GRCh37.p13 chr22: 30,718,804-30,719,113 TBC1D10A
    nsv5360492translocation1nstd200human GRCh38 chr22: 30,326,946-30,326,946 , GRCh38 chr22: 30,327,015-30,327,015 , GRCh37.p13 chr22: 30,723,004-30,723,004 , GRCh37.p13 chr22: 30,722,935-30,722,935 TBC1D10A
    nsv5031934copy number variation1nstd200human GRCh38 chr22: 30,325,636-30,356,897 , GRCh37.p13 chr22: 30,721,625-30,752,886 SF3A1, CCDC157, 1 more genes
    nsv4870957copy number variation1nstd200human GRCh37 chr22: 30,722,934-30,723,004 , GRCh38.p12 chr22: 30,326,945-30,327,015 TBC1D10A
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4676292copy number variation1nstd102humanPathogenic GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410 PDXP-DT, PDGFB, 550 more genes
    nsv4562195insertion1nstd166human GRCh37.p13 chr22: 30,704,298-30,704,298 , GRCh38.p12 chr22: 30,308,309-30,308,309 TBC1D10A
    nsv4534523copy number variation1nstd166human GRCh37.p13 chr22: 30,723,042-30,723,107 , GRCh38.p12 chr22: 30,327,053-30,327,118 TBC1D10A
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 IGLV3-27, XKR3, 1082 more genes
    nsv4436827inversion1nstd102humanLikely pathogenic GRCh38.p12 chr22: 29,288,727-31,344,669 , GRCh37 chr22: 29,684,716-31,740,655 AP1B1, EWSR1, 81 more genes
    nsv4383389copy number variation1nstd173human GRCh37 chr22: 21,465,662-33,984,045 , GRCh38.p12 chr22: 21,111,373-33,588,059 , XBP1, 450 more genes
    nsv4316382inversion1nstd166human GRCh37.p13 chr22: 22,466,414-30,881,792 , GRCh38.p12 chr22: 22,112,004-30,485,805 , CRYBB2, 313 more genes
    nsv4291884copy number variation1nstd166human GRCh37.p13 chr22: 30,720,000-30,725,000 , GRCh38.p12 chr22: 30,324,011-30,329,011 TBC1D10A
    nsv4287990copy number variation1nstd166human GRCh37.p13 chr22: 30,667,005-30,900,811 , GRCh38.p12 chr22: 30,271,016-30,504,824 , SEC14L3, 15 more genes
    nsv4284223copy number variation1nstd166human GRCh37.p13 chr22: 30,722,935-30,723,004 , GRCh38.p12 chr22: 30,326,946-30,327,015 TBC1D10A
    nsv3923324copy number variation1nstd102humanUncertain significance NCBI36 chr22: 29,038,245-29,676,302 , GRCh37 chr22: 30,708,245-31,346,302 , GRCh38 chr22: 30,312,256-30,950,316 SLC35E4, OSBP2, 28 more genes
    nsv3923205copy number variation1nstd102humanPathogenic NCBI36 chr22: 25,177,008-30,177,912 , GRCh37 chr22: 26,847,008-31,847,912 , GRCh38 chr22: 26,451,042-31,451,926 DRG1, THOC5, 138 more genes
    nsv3922708copy number variation1nstd102humanPathogenic GRCh38 chr22: 23,279,231-36,247,369 , GRCh37 chr22: 23,621,418-36,643,415 , NCBI36 chr22: 21,951,418-34,973,361 DRICH1, MMP11, 316 more genes
    nsv3919881copy number variation1nstd102humanPathogenic GRCh37 chr22: 17,397,633-51,178,213 , GRCh38 chr22: 16,916,743-50,739,785 , NCBI36 chr22: 15,777,633-49,525,079 MIR12114, MIR6820, 1059 more genes
    nsv3919429copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,661,724-32,217,179 , GRCh38 chr22: 18,178,957-31,821,193 , NCBI36 chr22: 17,041,724-30,547,179 PCAT14, MIR3199-1, 533 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