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Variant : CV382120 (GRCh37/hg19 15q13.1-13.3(chr15:29214105-32418220)x1) Homo sapiens

Symbol: CV382120
Name: GRCh37/hg19 15q13.1-13.3(chr15:29214105-32418220)x1
Condition: See cases [RCV000446254]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: APBA2   ARHGAP11B   CHRFAM7A   CHRNA7   FAM189A1   FAN1   GOLGA8H   GOLGA8J   KLF13   MIR211   MTMR10   NSMCE3   OTUD7A   TJP1   TRPM1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371529,214,105 - 32,418,220CLINVAR
Cytogenetic Map1515q13.1-13.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12850980
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2019-10-08
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.