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Variant : CV157842 (GRCh38/hg38 6q22.31-22.32(chr6:121829616-126154472)x1) Homo sapiens

Symbol: CV157842
Name: GRCh38/hg38 6q22.31-22.32(chr6:121829616-126154472)x1
Condition: See cases [RCV000137174]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CLVS2   FABP7   HDDC2   HEY2   HINT3   HSF2   LINC02523   NCOA7   NCOA7-AS1   NKAIN2   PKIB   RNF217   RNF217-AS1   SERINC1   SMPDL3A   TPD52L1   TRDN   TRDN-AS1   TRE-CTC1-7   TRMT11  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000006.12:g.(?_121829616)_(126154472_?)del
NC_000006.11:g.(?_122150762)_(126475618_?)del
NC_000006.10:g.(?_122192461)_(126517311_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh386121,829,616 - 126,154,472CLINVAR
GRCh376122,150,762 - 126,475,618CLINVAR
Build 366122,192,461 - 126,517,311CLINVAR
Cytogenetic Map66q22.31-22.32CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9484733
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-21
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.