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Variant : CV382351 (GRCh37/hg19 15q11.2(chr15:20733395-23487423)x3) Homo sapiens

Symbol: CV382351
Name: GRCh37/hg19 15q11.2(chr15:20733395-23487423)x3
Condition: See cases [RCV000449296]
Clinical Significance: benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: CYFIP1   GOLGA6L1   GOLGA6L6   NIPA1   NIPA2   OR4M2   OR4N4   POTEB   POTEB2   TUBGCP5  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371520,733,395 - 23,487,423CLINVAR
Cytogenetic Map1515q11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12853992
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2019-10-15
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.