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Variant : CV159082 (GRCh38/hg38 3p26.3-25.3(chr3:32241-11379835)x1) Homo sapiens

Symbol: CV159082
Name: GRCh38/hg38 3p26.3-25.3(chr3:32241-11379835)x1
Condition: See cases [RCV000138376]
Clinical Significance: pathogenic|likely benign
Last Evaluated: 07/11/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ARL8B   ARPC4   ARPC4-TTLL3   ATG7   ATP2B2   ATP2B2-IT2   BHLHE40   BHLHE40-AS1   BRK1   BRPF1   CAMK1   CAV3   CHL1   CHL1-AS1   CHL1-AS2   CIDEC   CNTN4   CNTN4-AS1   CNTN4-AS2   CNTN6   CPNE9   CRBN   CRELD1   EDEM1   EGOT   EMC3   EMC3-AS1   FANCD2   FANCD2OS   GHRL   GHRLOS   GRM7   GRM7-AS1   GRM7-AS2   GRM7-AS3   HRH1   IL17RC   IL17RE   IL5RA   IRAK2   ITPR1   ITPR1-DT   JAGN1   LHFPL4   LINC00312   LINC00606   LINC00852   LINC01266   LMCD1   LMCD1-AS1   LRRN1   MIR12127   MIR378B   MIR4790   MIR885   MTMR14   OGG1   OXTR   PRRT3   PRRT3-AS1   RAD18   RPUSD3   SEC13   SETD5   SETMAR   SLC6A1   SLC6A1-AS1   SLC6A11   SRGAP3   SRGAP3-AS2   SRGAP3-AS3   SRGAP3-AS4   SSUH2   SUMF1   TADA3   TATDN2   THUMPD3   THUMPD3-AS1   TRNT1   TTLL3   VHL  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_32241)_(11379835_?)del
NC_000003.11:g.(?_73914)_(11421309_?)del
NC_000003.10:g.(?_48914)_(11396309_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38332,241 - 11,379,835CLINVAR
GRCh37373,914 - 11,421,309CLINVAR
Build 36348,914 - 11,396,309CLINVAR
Cytogenetic Map33p26.3-25.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485925
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.