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Variant : CV155215 (GRCh38/hg38 8p23.1(chr8:7195674-7834323)x1) Homo sapiens

Symbol: CV155215
Name: GRCh38/hg38 8p23.1(chr8:7195674-7834323)x1
Condition: See cases [RCV000134832]
Clinical Significance: benign
Last Evaluated: 09/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: DEFB103B   DEFB104B   DEFB105A   DEFB105B   DEFB106A   DEFB106B   DEFB107A   DEFB107B   DEFB109B   DEFB4B   FAM66B   LINC00965   PRR23D1   PRR23D2   SPAG11B   USP17L1   USP17L4   ZNF705G  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_7195674)_(7834323_?)del
NC_000008.10:g.(?_7053196)_(7691845_?)del
NC_000008.9:g.(?_7040606)_(7729255_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3887,195,674 - 7,834,323CLINVAR
GRCh3787,053,196 - 7,691,845CLINVAR
Build 3687,040,606 - 7,729,255CLINVAR
Cytogenetic Map88p23.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482409
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-08-04
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.