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Variant : CV673770 (GRCh37/hg19 13q34(chr13:111568865-115107733)x1) Homo sapiens

Symbol: CV673770
Name: GRCh37/hg19 13q34(chr13:111568865-115107733)x1
Condition: not provided [RCV000846886]
Clinical Significance: pathogenic
Last Evaluated: 10/26/2017
Review Status: no assertion criteria provided
Related Genes: ADPRHL1   ARHGEF7   ATP11A   ATP11AUN   ATP4B   CDC16   CHAMP1   CUL4A   DCUN1D2   F10   F7   GAS6   GRTP1   LAMP1   LINC00565   MCF2L   PCID2   PROZ   RASA3   SOX1   SPACA7   TEX29   TFDP1   TMCO3   TMEM255B   TUBGCP3   UPF3A  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3713111,568,865 - 115,107,733CLINVAR
Cytogenetic Map1313q34CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14977462
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-01-14
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.