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Variant : CV674690 (GRCh37/hg19 8p22-21.3(chr8:18266233-20864195)x1) Homo sapiens

Symbol: CV674690
Name: GRCh37/hg19 8p22-21.3(chr8:18266233-20864195)x1
Condition: not provided [RCV000847806]
Clinical Significance: uncertain significance
Last Evaluated: 06/30/2017
Review Status: no assertion criteria provided
Related Genes: ATP6V1B2   CSGALNACT1   INTS10   LPL   LZTS1   PSD3   SH2D4A   SLC18A1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37818,266,233 - 20,864,195CLINVAR
Cytogenetic Map88p22-21.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14979335
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-06-30
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.