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 77

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5281292copy number variation1nstd204human GRCh38.p13 chr22: 41,124,301-41,900,100 , GRCh37.p13 chr22: 41,520,305-42,296,104 SNU13, RANGAP1, 34 more genes
    nsv5034253copy number variation1nstd200human GRCh38 chr22: 41,706,511-41,712,835 , GRCh37.p13 chr22: 42,102,515-42,108,839 HMGN2P10, MEI1
    nsv5032425inversion1nstd200human GRCh38 chr22: 41,452,969-44,153,937 , GRCh37.p13 chr22: 41,848,973-44,549,817 , LOC101927393, 95 more genes
    nsv5031848copy number variation1nstd200human GRCh38 chr22: 41,692,369-41,719,697 , GRCh37.p13 chr22: 42,088,373-42,115,701 C22orf46P, HMGN2P10, 1 more genes
    nsv4877290copy number variation1nstd200human GRCh37 chr22: 42,102,515-42,108,839 , GRCh38.p12 chr22: 41,706,511-41,712,835 MEI1, HMGN2P10
    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
    nsv4729846copy number variation1nstd102humanUncertain significance GRCh37 chr22: 41,853,620-42,385,978 , GRCh38.p12 chr22: 41,457,616-41,989,974 RNU6ATAC22P, CSDC2, 23 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
    nsv4676232copy number variation1nstd102humanPathogenic GRCh37 chr22: 40,502,364-51,197,838 , GRCh38.p12 chr22: 40,106,360-50,759,410 MIR378I, SNORD13P1, 274 more genes
    nsv4623773copy number variation1nstd183human GRCh37 chr22: 42,091,077-42,114,496 , GRCh38.p12 chr22: 41,695,073-41,718,492 MEI1, C22orf46P, 1 more genes
    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
    nsv4384202copy number variation1nstd173human GRCh37 chr22: 42,089,094-42,112,295 , GRCh38.p12 chr22: 41,693,090-41,716,291 HMGN2P10, C22orf46P, 1 more genes
    nsv3924136copy number variation1nstd102humanPathogenic GRCh38 chr22: 40,202,014-50,735,806 , GRCh37 chr22: 40,598,018-51,174,234 , NCBI36 chr22: 38,927,964-49,521,100 CYP2D8P, TBC1D22A-AS1, 270 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
    nsv3919563copy number variation1nstd102humanUncertain significance GRCh38 chr22: 41,645,339-42,565,798 , NCBI36 chr22: 40,371,289-41,291,748 , GRCh37 chr22: 42,041,343-42,961,804 OLA1P1, NFAM1, 41 more genes
    nsv3919085copy number variation1nstd102humanPathogenic NCBI36 chr22: 17,008,132-49,591,432 , GRCh37.p13 chr22: 18,628,132-51,244,566 , GRCh38.p12 chr22: 18,145,365-50,806,138 IGLV2-28, LINC01310, 1023 more genes
    nsv3913775copy number variation1nstd102humanPathogenic NCBI36 chr22: 15,777,498-49,525,130 , GRCh38 chr22: 16,916,608-50,739,836 , GRCh37 chr22: 17,397,498-51,178,264 ZNF280A, RFPL1S, 1059 more genes
    nsv3911730copy number variation1nstd102humanPathogenic NCBI36 chr22: 40,003,772-41,140,907 , GRCh38 chr22: 41,277,822-42,414,957 , GRCh37 chr22: 41,673,826-42,810,963 LOC105373044, CENPM, 50 more genes
    nsv3910659copy number variation1nstd102humanPathogenic NCBI36 chr22: 37,642,438-49,574,364 , GRCh37.p13 chr22: 39,312,492-51,227,498 , GRCh38.p12 chr22: 38,916,487-50,789,070 LOC100506472, MCHR1, 314 more genes
    nsv3910634copy number variation1nstd102humanPathogenic GRCh38 chr22: 37,061,769-50,738,932 , NCBI36 chr22: 35,787,755-49,524,226 , GRCh37 chr22: 37,457,809-51,177,360 HDAC10, RPS25P10, 381 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