Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV157101 (GRCh38/hg38 7q11.23(chr7:75568161-76584760)x1) Homo sapiens

Symbol: CV157101
Name: GRCh38/hg38 7q11.23(chr7:75568161-76584760)x1
Condition: See cases [RCV000136550]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC004980.1   CCL24   CCL26   DTX2   HIP1   HSPB1   MDH2   MIR4651   POR   RHBDD2   SNORA14A   SPDYE16   SRRM3   SSC4D   STYXL1   TMEM120A   UPK3B   YWHAG   ZP3  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_75568161)_(76584760_?)del
NC_000007.13:g.(?_75197465)_(76214077_?)del
NC_000007.12:g.(?_75035401)_(76052013_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38775,568,161 - 76,584,760CLINVAR
GRCh37775,197,465 - 76,214,077CLINVAR
Build 36775,035,401 - 76,052,013CLINVAR
Cytogenetic Map77q11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9484111
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-28
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.