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Variant : CV155152 (GRCh38/hg38 4p16.3(chr4:37335-3775112)x1) Homo sapiens

Symbol: CV155152
Name: GRCh38/hg38 4p16.3(chr4:37335-3775112)x1
Condition: See cases [RCV000134785]
Clinical Significance: pathogenic
Last Evaluated: 08/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC092535.4   AC116565.1   AC139887.2   ADD1   ADRA2C   ATP5ME   C4orf48   CFAP99   CPLX1   CTBP1   CTBP1-AS   CTBP1-DT   DGKQ   DOK7   FAM193A   FAM53A   FGFR3   FGFRL1   GAK   GRK4   HAUS3   HGFAC   HTT   HTT-AS   IDUA   LETM1   LINC00955   LINC02171   LRPAP1   MAEA   MFSD10   MIR4800   MIR571   MIR943   MSANTD1   MXD4   MYL5   NAT8L   NELFA   NKX1-1   NOP14   NOP14-AS1   NSD2   PCGF3   PDE6B   PDE6B-AS1   PIGG   POLN   RGS12   RNF212   RNF4   SCARNA22   SH3BP2   SLBP   SLC26A1   SLC49A3   SPON2   TACC3   TMEM129   TMEM175   TMEM271   TNIP2   UVSSA   ZFYVE28   ZNF141   ZNF595   ZNF718   ZNF721   ZNF732  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000004.12:g.(?_37335)_(3775112_?)del
NC_000004.11:g.(?_37336)_(3776839_?)del
NC_000004.10:g.(?_27336)_(3746637_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38437,335 - 3,775,112CLINVAR
GRCh37437,336 - 3,776,839CLINVAR
Build 36427,336 - 3,746,637CLINVAR
Cytogenetic Map44p16.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9482362
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-09-08
Status: ACTIVE



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