Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV159610 (GRCh38/hg38 12q23.3(chr12:103500125-104726872)x1) Homo sapiens

Symbol: CV159610
Name: GRCh38/hg38 12q23.3(chr12:103500125-104726872)x1
Condition: See cases [RCV000138809]
Clinical Significance: uncertain significance
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: C12orf42   C12orf73   CHST11   EID3   GLT8D2   HCFC2   HSP90B1   LINC02385   LINC02401   MIR3652   MIR3922   NFYB   NT5DC3   STAB2   TDG   TXNRD1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000012.12:g.(?_103500125)_(104726872_?)del
NC_000012.11:g.(?_103893903)_(105120650_?)del
NC_000012.10:g.(?_102418033)_(103644780_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3812103,500,125 - 104,726,872CLINVAR
GRCh3712103,893,903 - 105,120,650CLINVAR
Build 3612102,418,033 - 103,644,780CLINVAR
Cytogenetic Map1212q23.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9486346
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-30
Status: ACTIVE



NHLBI Logo

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