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Variant : CV555162 (GRCh37/hg19 12q21.31-21.32(chr12:86115942-88186381)x1) Homo sapiens

Symbol: CV555162
Name: GRCh37/hg19 12q21.31-21.32(chr12:86115942-88186381)x1
Condition: not provided [RCV000683467]
Clinical Significance: uncertain significance
Last Evaluated: 07/26/2017
Review Status: no assertion criteria provided
Related Genes: MGAT4C   NTS   RASSF9  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371286,115,942 - 88,186,381CLINVAR
Cytogenetic Map1212q21.31-21.32CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13796897
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-05-26
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.