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Variant : CV155824 (GRCh38/hg38 10q26.3(chr10:132178475-133620674)x1) Homo sapiens

Symbol: CV155824
Name: GRCh38/hg38 10q26.3(chr10:132178475-133620674)x1
Condition: See cases [RCV000135399]
Clinical Significance: pathogenic
Last Evaluated: 07/30/2009
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADAM8   ADGRA1   ADGRA1-AS1   CALY   CFAP46   CYP2E1   DPYSL4   ECHS1   FUOM   INPP5A   JAKMIP3   KNDC1   LINC01165   LINC01166   LINC01167   LINC01168   LINC02870   LRRC27   MIR202   MIR202HG   MIR3944   MTG1   NKX6-2   PAOX   PRAP1   PWWP2B   SPRN   STK32C   SYCE1   TUBGCP2   UTF1   VENTX   ZNF511  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_132178475)_(133620674_?)del
NC_000010.10:g.(?_133991979)_(135434178_?)del
NC_000010.9:g.(?_133841969)_(135284168_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3810132,178,475 - 133,620,674CLINVAR
GRCh3710133,991,979 - 135,434,178CLINVAR
Build 3610133,841,969 - 135,284,168CLINVAR
Cytogenetic Map1010q26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482972
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-20
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.