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Variant : CV673817 (GRCh37/hg19 4q21.1-21.23(chr4:78769297-84968832)x1) Homo sapiens

Symbol: CV673817
Name: GRCh37/hg19 4q21.1-21.23(chr4:78769297-84968832)x1
Condition: not provided [RCV000846933]
Clinical Significance: pathogenic
Last Evaluated: 10/31/2017
Review Status: no assertion criteria provided
Related Genes: ABRAXAS1   ANTXR2   ANXA3   BMP2K   BMP3   CFAP299   COPS4   COQ2   ENOPH1   FGF5   FRAS1   GK2   GPAT3   HELQ   HNRNPD   HNRNPDL   HPSE   LIN54   MRPL1   MRPS18C   NAA11   PAQR3   PCAT4   PLAC8   PRDM8   PRKG2   RASGEF1B   SCD5   SEC31A   THAP9   TMEM150C  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37478,769,297 - 84,968,832CLINVAR
Cytogenetic Map44q21.1-21.23CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14977507
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.