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Variant : CV155899 (GRCh38/hg38 14q11.2(chr14:21973760-22442515)x1) Homo sapiens

Symbol: CV155899
Name: GRCh38/hg38 14q11.2(chr14:21973760-22442515)x1
Condition: See cases [RCV000135471]
Clinical Significance: benign
Last Evaluated: 07/30/2009
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: TRA   TRAV16   TRAV17   TRAV18   TRAV19   TRAV20   TRAV21   TRAV22   TRAV23DV6   TRAV24   TRAV25   TRAV26-1   TRAV26-2   TRAV27   TRAV29DV5   TRAV30   TRAV34   TRAV35   TRAV36DV7   TRAV38-1   TRAV38-2DV8   TRAV39   TRAV40   TRAV41   TRAV8-6   TRAV8-7   TRD   TRDD1   TRDD2   TRDV1   TRDV2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000014.9:g.(?_21973760)_(22442515_?)del
NC_000014.8:g.(?_22441989)_(22911507_?)del
NC_000014.7:g.(?_21511829)_(21981347_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381421,973,760 - 22,442,515CLINVAR
GRCh371422,441,989 - 22,911,507CLINVAR
Build 361421,511,829 - 21,981,347CLINVAR
Cytogenetic Map1414q11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483044
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-11-12
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.