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Variant : CV162867 (GRCh38/hg38 13q13.2-13.3(chr13:34151122-35159055)x1) Homo sapiens

Symbol: CV162867
Name: GRCh38/hg38 13q13.2-13.3(chr13:34151122-35159055)x1
Condition: See cases [RCV000141615]
Clinical Significance: uncertain significance
Last Evaluated: 09/16/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC00457   LINC02343   NBEA  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000013.11:g.(?_34151122)_(35159055_?)del
NC_000013.10:g.(?_34725259)_(35733192_?)del
NC_000013.9:g.(?_33623259)_(34631192_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381334,151,122 - 35,159,055CLINVAR
GRCh371334,725,259 - 35,733,192CLINVAR
Build 361333,623,259 - 34,631,192CLINVAR
Cytogenetic Map1313q13.2-13.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489140
Created: 2014-09-09
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.