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Variant : CV437459 (GRCh37/hg19 3p26.2-26.1(chr3:2930451-5953602)x1) Homo sapiens

Symbol: CV437459
Name: GRCh37/hg19 3p26.2-26.1(chr3:2930451-5953602)x1
Condition: See cases [RCV000512359]
Clinical Significance: pathogenic
Last Evaluated: 05/22/2013
Review Status: no assertion criteria provided
Related Genes: ARL8B   BHLHE40   CNTN4   CRBN   EDEM1   EGOT   IL5RA   ITPR1   LRRN1   SETMAR   SUMF1   TRNT1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3732,930,451 - 5,953,602CLINVAR
Cytogenetic Map33p26.2-26.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13445322
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-11-12
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.