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Variant : CV803293 (GRCh37/hg19 8p23.1(chr8:6999219-8641125)x3) Homo sapiens

Symbol: CV803293
Name: GRCh37/hg19 8p23.1(chr8:6999219-8641125)x3
Condition: not provided [RCV001006061]
Clinical Significance: uncertain significance
Last Evaluated: 11/13/2018
Review Status: no assertion criteria provided
Related Genes: CLDN23   DEFB103A   DEFB103B   DEFB104A   DEFB104B   DEFB105A   DEFB105B   DEFB106A   DEFB106B   DEFB107A   DEFB107B   DEFB4A   DEFB4B   SPAG11A   SPAG11B   USP17L1   USP17L3   USP17L4   USP17L8   ZNF705B   ZNF705G  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3786,999,219 - 8,641,125CLINVAR
Cytogenetic Map88p23.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 25320725
Created: 2020-04-07
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.