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Variant : CV673261 (GRCh37/hg19 8p12(chr8:29103983-35728509)x1) Homo sapiens

Symbol: CV673261
Name: GRCh37/hg19 8p12(chr8:29103983-35728509)x1
Condition: not provided [RCV000846377]
Clinical Significance: uncertain significance
Last Evaluated: 01/22/2018
Review Status: no assertion criteria provided
Related Genes: DCTN6   DUSP26   DUSP4   FUT10   GSR   GTF2E2   KIF13B   LEPROTL1   MAK16   MBOAT4   NRG1   PPP2CB   PURG   RBPMS   RNF122   SARAF   SMIM18   TEX15   TTI2   UBXN8   UNC5D   WRN  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37829,103,983 - 35,728,509CLINVAR
Cytogenetic Map88p12CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 14976280
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-03-31
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.