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Variant : CV602621 (GRCh37/hg19 8q24.3(chr8:144056476-144733805)x1) Homo sapiens

Symbol: CV602621
Name: GRCh37/hg19 8q24.3(chr8:144056476-144733805)x1
Condition: not provided [RCV000747921]
Clinical Significance: benign
Last Evaluated: 01/24/2011
Review Status: no assertion criteria provided
Related Genes: C8orf31   EEF1D   GFUS   GLI4   GPIHBP1   GSDMD   LY6E   LY6H   MAFA   MROH6   NAPRT   PYCR3   RHPN1   TIGD5   TOP1MT   ZC3H3   ZFP41   ZNF623   ZNF696  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh378144,056,476 - 144,733,805CLINVAR
Cytogenetic Map88q24.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14363266
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-05-19
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.