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Variant : CV156646 (GRCh38/hg38 22q13.31-13.33(chr22:43992879-50683114)x3) Homo sapiens

Symbol: CV156646
Name: GRCh38/hg38 22q13.31-13.33(chr22:43992879-50683114)x3
Condition: See cases [RCV000136124]
Clinical Significance: benign
Last Evaluated: 10/01/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADM2   AL079301.1   AL117329.1   ALG12   ARHGAP8   ARSA   ATXN10   BRD1   C22orf34   CDPF1   CELSR1   CERK   CHKB   CHKB-CPT1B   CHKB-DT   CPT1B   CRELD2   DENND6B   FAM118A   FBLN1   GRAMD4   GTSE1   GTSE1-DT   HDAC10   IL17REL   KIAA0930   KLHDC7B   KLHDC7B-DT   LINC00207   LINC00229   LINC00898   LINC00899   LINC01310   LINC01589   LINC01644   LINC01656   LMF2   MAPK11   MAPK12   MAPK8IP2   MIOX   MIR12114   MIR1249   MIR3201   MIR3619   MIR3667   MIR4535   MIR4762   MIR4763   MIR6821   MIRLET7A3   MIRLET7B   MIRLET7BHG   MLC1   MOV10L1   NCAPH2   NUP50   NUP50-DT   ODF3B   PANX2   PARVB   PARVG   PHF21B   PIM3   PKDREJ   PLXNB2   PPARA   PPP6R2   PRR34   PRR34-AS1   PRR5   PRR5-ARHGAP8   RIBC2   RTL6   SAMM50   SBF1   SCO2   SELENOO   SHANK3   SHISAL1   SMC1B   SYCE3   TAFA5   TBC1D22A   TBC1D22A-AS1   TRABD   TRMU   TRU-TCA2-1   TTC38   TTLL8   TUBGCP6   TYMP   UPK3A   WNT7B   Z82186.1   Z84468.1   ZBED4  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000022.11:g.(?_43992879)_(50683114_?)dup
Human AssemblyChrPosition (strand)Source
GRCh382243,992,879 - 50,683,114CLINVAR
GRCh372244,388,759 - 51,121,542CLINVAR
Build 362242,720,092 - 49,468,408CLINVAR
Cytogenetic Map2222q13.31-13.33CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 9483686
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-30
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.