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Variant : CV550759 (NC_000019.9:g.10132458_10230550dup) Homo sapiens

Symbol: CV550759
Name: NC_000019.9:g.10132458_10230550dup
Condition: not provided [RCV000677920]
Clinical Significance: uncertain significance
Last Evaluated: 02/26/2018
Review Status: criteria provided, single submitter
Related Genes: ANGPTL6   EIF3G   P2RY11   PPAN   PPAN-P2RY11   RDH8   SHFL  
Variant Type: duplication (SO:1000035)
Source: CLINVAR
Evidence: provider interpretation
HGVS Name(s): NC_000019.9:g.10132458_10230550dup
Position
Human AssemblyChrPosition (strand)Source
GRCh371910,132,458 - 10,230,550CLINVAR
Cytogenetic Map1919p13.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13785920
Created: 2018-09-11
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.