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Variant : CV154288 (GRCh38/hg38 8p23.1(chr8:7256134-7294303)x1) Homo sapiens

Symbol: CV154288
Name: GRCh38/hg38 8p23.1(chr8:7256134-7294303)x1
Condition: See cases [RCV000134019]
Clinical Significance: benign
Last Evaluated: 05/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC00965  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_7256134)_(7294303_?)del
NC_000008.10:g.(?_7113656)_(7151825_?)del
NC_000008.9:g.(?_7101066)_(7139235_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3887,256,134 - 7,294,303CLINVAR
GRCh3787,113,656 - 7,151,825CLINVAR
Build 3687,101,066 - 7,139,235CLINVAR
Cytogenetic Map88p23.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9481604
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.