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Variant : CV161285 (GRCh38/hg38 3p26.3-25.3(chr3:32241-9574994)x1) Homo sapiens

Symbol: CV161285
Name: GRCh38/hg38 3p26.3-25.3(chr3:32241-9574994)x1
Condition: See cases [RCV000140239]
Clinical Significance: pathogenic
Last Evaluated: 10/09/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ARL8B   BHLHE40   BHLHE40-AS1   CAV3   CHL1   CHL1-AS1   CHL1-AS2   CNTN4   CNTN4-AS1   CNTN4-AS2   CNTN6   CRBN   EDEM1   EGOT   GRM7   GRM7-AS1   GRM7-AS2   GRM7-AS3   IL5RA   ITPR1   ITPR1-DT   LHFPL4   LINC00312   LINC01266   LMCD1   LMCD1-AS1   LRRN1   MIR4790   OXTR   RAD18   SETD5   SETMAR   SRGAP3   SRGAP3-AS2   SRGAP3-AS3   SRGAP3-AS4   SSUH2   SUMF1   THUMPD3   THUMPD3-AS1   TRNT1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_32241)_(9574994_?)del
NC_000003.11:g.(?_73914)_(9616678_?)del
NC_000003.10:g.(?_48914)_(9591678_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38332,241 - 9,574,994CLINVAR
GRCh37373,914 - 9,616,678CLINVAR
Build 36348,914 - 9,591,678CLINVAR
Cytogenetic Map33p26.3-25.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487769
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-04
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.