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Variant : CV437087 (GRCh37/hg19 14q24.1-24.2(chr14:68035240-73568130)x1) Homo sapiens

Symbol: CV437087
Name: GRCh37/hg19 14q24.1-24.2(chr14:68035240-73568130)x1
Condition: See cases [RCV000512344]
Clinical Significance: likely pathogenic
Last Evaluated: 08/25/2014
Review Status: no assertion criteria provided
Related Genes: ACTN1   ADAM20   ADAM21   ARG2   CCDC177   COX16   DCAF4   DCAF5   DPF3   ERH   EXD2   GALNT16   MAP3K9   MED6   PCNX1   PIGH   PLEKHD1   PLEKHH1   RAD51B   RBM25   RDH11   RDH12   RGS6   SIPA1L1   SLC10A1   SLC39A9   SLC8A3   SMOC1   SRSF5   SUSD6   SYNJ2BP   TTC9   VTI1B   ZFP36L1   ZFYVE1   ZFYVE26  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371468,035,240 - 73,568,130CLINVAR
Cytogenetic Map1414q24.1-24.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13445309
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.