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Variant : CV156429 (GRCh38/hg38 7q11.23(chr7:75529854-76626561)x3) Homo sapiens

Symbol: CV156429
Name: GRCh38/hg38 7q11.23(chr7:75529854-76626561)x3
Condition: See cases [RCV000135929]
Clinical Significance: uncertain significance
Last Evaluated: 02/25/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC004980.1   CCL24   CCL26   DTX2   HIP1   HSPB1   MDH2   MIR4651   POMZP3   POR   RHBDD2   SNORA14A   SPDYE16   SRRM3   SSC4D   STYXL1   TMEM120A   UPK3B   YWHAG   ZP3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_75529854)_(76626561_?)dup
NC_000007.13:g.(?_75159180)_(76255878_?)dup
NC_000007.12:g.(?_74997116)_(76093814_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38775,529,854 - 76,626,561CLINVAR
GRCh37775,159,180 - 76,255,878CLINVAR
Build 36774,997,116 - 76,093,814CLINVAR
Cytogenetic Map77q11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9483495
Created: 2014-09-09
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.