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Variant : CV436969 (GRCh37/hg19 8q13.3(chr8:71198990-71920676)x1) Homo sapiens

Symbol: CV436969
Name: GRCh37/hg19 8q13.3(chr8:71198990-71920676)x1
Condition: See cases [RCV000512294]
Clinical Significance: uncertain significance
Last Evaluated: 07/06/2015
Review Status: no assertion criteria provided
Related Genes: LACTB2   NCOA2   TRAM1   XKR9  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37871,198,990 - 71,920,676CLINVAR
Cytogenetic Map88q13.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13445260
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-03-24
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.