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Variant : CV73491 (GRCh38/hg38 7q11.23(chr7:75769688-76066509)x1) Homo sapiens

Symbol: CV73491
Name: GRCh38/hg38 7q11.23(chr7:75769688-76066509)x1
Condition: See cases [RCV000052686]
Clinical Significance: uncertain significance
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: CCL24   CCL26   MDH2   MIR4651   POR   RHBDD2   SNORA14A   STYXL1   TMEM120A  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_75769688)_(76066509_?)del
NW_003871064.1:g.(?_3298924)_(3595745_?)del
NC_000007.12:g.(?_75236942)_(75533763_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38775,769,688 - 76,066,509CLINVAR
Build 36775,236,942 - 75,533,763CLINVAR
Cytogenetic Map77q11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 8619661
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2020-07-28
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.