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Variant : CV436459 (GRCh37/hg19 4q21.21-21.23(chr4:82359656-84155605)x1) Homo sapiens

Symbol: CV436459
Name: GRCh37/hg19 4q21.21-21.23(chr4:82359656-84155605)x1
Condition: See cases [RCV000511583]
Clinical Significance: likely pathogenic
Last Evaluated: 06/22/2015
Review Status: no assertion criteria provided
Related Genes: COPS4   ENOPH1   HNRNPD   HNRNPDL   LIN54   PLAC8   RASGEF1B   SCD5   SEC31A   THAP9   TMEM150C  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37482,359,656 - 84,155,605CLINVAR
Cytogenetic Map44q21.21-21.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13444553
Created: 2017-11-07
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.