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Variant : CV675410 (GRCh37/hg19 7q11.23(chr7:75091878-76117614)x1) Homo sapiens

Symbol: CV675410
Name: GRCh37/hg19 7q11.23(chr7:75091878-76117614)x1
Condition: not provided [RCV000848509]
Clinical Significance: uncertain significance
Last Evaluated: 08/22/2018
Review Status: no assertion criteria provided
Related Genes: CCL24   CCL26   DTX2   HIP1   HSPB1   MDH2   POM121C   POR   RHBDD2   SPDYE5   SRRM3   SSC4D   STYXL1   TMEM120A   YWHAG   ZP3  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37775,091,878 - 76,117,614CLINVAR
Cytogenetic Map77q11.23CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14980060
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-01-07
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.