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Variant : CV160761 (GRCh38/hg38 8p23.1(chr8:8253505-9758024)x1) Homo sapiens

Symbol: CV160761
Name: GRCh38/hg38 8p23.1(chr8:8253505-9758024)x1
Condition: See cases [RCV000139792]
Clinical Significance: uncertain significance
Last Evaluated: 06/01/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC022784.1   CLDN23   ERI1   MFHAS1   MIR4660   MIR597   PPP1R3B   PRAG1   SNORD3I   TNKS  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_8253505)_(9758024_?)del
NC_000008.10:g.(?_8111027)_(9615534_?)del
NC_000008.9:g.(?_8148437)_(9652944_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3888,253,505 - 9,758,024CLINVAR
GRCh3788,111,027 - 9,615,534CLINVAR
Build 3688,148,437 - 9,652,944CLINVAR
Cytogenetic Map88p23.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487322
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-30
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.