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Variant : CV673562 (GRCh37/hg19 12q23.2-23.3(chr12:102414522-105845768)x1) Homo sapiens

Symbol: CV673562
Name: GRCh37/hg19 12q23.2-23.3(chr12:102414522-105845768)x1
Condition: not provided [RCV000846678]
Clinical Significance: uncertain significance
Last Evaluated: 12/27/2017
Review Status: no assertion criteria provided
Related Genes: ALDH1L2   APPL2   ASCL1   C12orf42   C12orf45   C12orf73   C12orf75   CHST11   EID3   GLT8D2   HCFC2   HSP90B1   IGF1   NFYB   NT5DC3   NUP37   PAH   PARPBP   PMCH   SLC41A2   STAB2   TDG   TXNRD1   WASHC3   WASHC4  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3712102,414,522 - 105,845,768CLINVAR
Cytogenetic Map1212q23.2-23.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14977247
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-01-14
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.