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Variant : CV554860 (GRCh37/hg19 9q21.13-21.31(chr9:74534790-84014155)x1) Homo sapiens

Symbol: CV554860
Name: GRCh37/hg19 9q21.13-21.31(chr9:74534790-84014155)x1
Condition: not provided [RCV000683165]
Clinical Significance: pathogenic
Last Evaluated: 03/29/2018
Review Status: no assertion criteria provided
Related Genes: ALDH1A1   ANXA1   C9orf40   C9orf57   C9orf85   CARNMT1   CARNMT1-AS1   CEP78   FOXB2   GCNT1   GDA   GNA14   GNAQ   NMRK1   OSTF1   PCA3   PCSK5   PRUNE2   PSAT1   RFK   RORB   TLE4   TMC1   TRPM6   VPS13A   ZFAND5  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37974,534,790 - 84,014,155CLINVAR
Cytogenetic Map99q21.13-21.31CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13796102
Created: 2018-10-09
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.