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Variant : CV156440 (GRCh38/hg38 13q12.12(chr13:22822881-23533846)x1) Homo sapiens

Symbol: CV156440
Name: GRCh38/hg38 13q12.12(chr13:22822881-23533846)x1
Condition: See cases [RCV000135940]
Clinical Significance: uncertain significance
Last Evaluated: 02/25/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC00327   LINC00621   SACS   SACS-AS1   SGCG  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000013.11:g.(?_22822881)_(23533846_?)del
NC_000013.10:g.(?_23397020)_(24107985_?)del
NC_000013.9:g.(?_22295020)_(23005985_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381322,822,881 - 23,533,846CLINVAR
GRCh371323,397,020 - 24,107,985CLINVAR
Build 361322,295,020 - 23,005,985CLINVAR
Cytogenetic Map1313q12.12CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483506
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.