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Variant : CV675491 (GRCh37/hg19 11p15.1(chr11:16775884-18418719)x3) Homo sapiens

Symbol: CV675491
Name: GRCh37/hg19 11p15.1(chr11:16775884-18418719)x3
Condition: not provided [RCV000848590]
Clinical Significance: uncertain significance
Last Evaluated: 06/26/2018
Review Status: no assertion criteria provided
Related Genes: ABCC8   C11orf58   GTF2H1   HPS5   KCNC1   KCNJ11   LDHA   MRGPRX3   MRGPRX4   MYOD1   NCR3LG1   NUCB2   OTOG   PIK3C2A   PLEKHA7   RPS13   SAA1   SAA2   SAA2-SAA4   SAA4   SAAL1   SERGEF   TPH1   USH1C  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371116,775,884 - 18,418,719CLINVAR
Cytogenetic Map1111p15.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14980135
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-06-30
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.