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Variant : CV674274 (GRCh37/hg19 12q21.31-21.32(chr12:86138213-88183106)x1) Homo sapiens

Symbol: CV674274
Name: GRCh37/hg19 12q21.31-21.32(chr12:86138213-88183106)x1
Condition: not provided [RCV000847390]
Clinical Significance: uncertain significance
Last Evaluated: 11/14/2017
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
GRCh371286,138,213 - 88,183,106CLINVAR
Cytogenetic Map1212q21.31-21.32CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14978016
Created: 2019-10-08
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.