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Variant : CV72168 (GRCh38/hg38 7q11.23(chr7:75526437-76499472)x1) Homo sapiens

Symbol: CV72168
Name: GRCh38/hg38 7q11.23(chr7:75526437-76499472)x1
Condition: See cases [RCV000051302]
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   DTX2   HIP1   HSPB1   MDH2   MIR4651   POR   RHBDD2   SNORA14A   SRRM3   SSC4D   STYXL1   TMEM120A   YWHAG   ZP3  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_75526437)_(76499472_?)del
NC_000007.13:g.(?_75155767)_(76128789_?)del
NC_000007.12:g.(?_74993703)_(75966725_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38775,526,437 - 76,499,472CLINVAR
GRCh37775,155,767 - 76,128,789CLINVAR
Build 36774,993,703 - 75,966,725CLINVAR
Cytogenetic Map77q11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 8618327
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.