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Variant : CV159717 (GRCh38/hg38 6p21.31(chr6:33836334-34176285)x1) Homo sapiens

Symbol: CV159717
Name: GRCh38/hg38 6p21.31(chr6:33836334-34176285)x1
Condition: See cases [RCV000138894]
Clinical Significance: uncertain significance
Last Evaluated: 06/01/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: GRM4   LINC01016   MIR1275   MIR7159  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000006.12:g.(?_33836334)_(34176285_?)del
NC_000006.11:g.(?_33804111)_(34144062_?)del
NC_000006.10:g.(?_33912089)_(34252040_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38633,836,334 - 34,176,285CLINVAR
GRCh37633,804,111 - 34,144,062CLINVAR
Build 36633,912,089 - 34,252,040CLINVAR
Cytogenetic Map66p21.31CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9486427
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-21
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.