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Variant : CV381400 (GRCh37/hg19 10q24.32-24.33(chr10:104853173-105357653)x4) Homo sapiens

Symbol: CV381400
Name: GRCh37/hg19 10q24.32-24.33(chr10:104853173-105357653)x4
Condition: See cases [RCV000448445]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ATP5MD   CALHM1   CALHM2   CALHM3   INA   NEURL1   NT5C2   PCGF6   PDCD11   SH3PXD2A   TAF5  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710104,853,173 - 105,357,653CLINVAR
Cytogenetic Map1010q24.32-24.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12853153
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-01-14
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.