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Variant : CV605606 (GRCh37/hg19 13q34(chr13:111217422-115103529)x1) Homo sapiens

Symbol: CV605606
Name: GRCh37/hg19 13q34(chr13:111217422-115103529)x1
Condition: not provided [RCV000750906]
Clinical Significance: pathogenic
Last Evaluated: 10/16/2013
Review Status: no assertion criteria provided
Related Genes: ADPRHL1   ANKRD10   ANKRD10-IT1   ARHGEF7   ATP11A   ATP11AUN   ATP4B   CARS2   CDC16   CHAMP1   CUL4A   DCUN1D2   F10   F7   GAS6   GRTP1   ING1   LAMP1   LINC00565   LINC00567   MCF2L   NAXD   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
GRCh3713111,217,422 - 115,103,529CLINVAR
Cytogenetic Map1313q34CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14366232
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-21
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.