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Variant : CV382915 (GRCh37/hg19 10q24.33(chr10:105045727-105206874)x3) Homo sapiens

Symbol: CV382915
Name: GRCh37/hg19 10q24.33(chr10:105045727-105206874)x3
Condition: See cases [RCV000449058]
Clinical Significance: likely benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ATP5MD   CALHM2   INA   PCGF6   PDCD11   TAF5  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710105,045,727 - 105,206,874CLINVAR
Cytogenetic Map1010q24.33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12853757
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-01-21
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.