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Variant : CV436416 (GRCh37/hg19 16q22.1(chr16:69369131-69941373)x3) Homo sapiens

Symbol: CV436416
Name: GRCh37/hg19 16q22.1(chr16:69369131-69941373)x3
Condition: See cases [RCV000511639]
Clinical Significance: uncertain significance
Last Evaluated: 02/16/2015
Review Status: no assertion criteria provided
Related Genes: COG8   CYB5B   NFAT5   NIP7   NOB1   NQO1   TERF2   TMED6   WWP2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371669,369,131 - 69,941,373CLINVAR
Cytogenetic Map1616q22.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13444609
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-11-12
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.