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Variant : CV596742 (GRCh37/hg19 22q13.31(chr22:46487902-46536003)x1) Homo sapiens

Symbol: CV596742
Name: GRCh37/hg19 22q13.31(chr22:46487902-46536003)x1
Condition: not provided [RCV000742042]
Clinical Significance: benign
Last Evaluated: 11/01/2011
Review Status: no assertion criteria provided
Related Genes: MIRLET7A3   MIRLET7B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372246,487,902 - 46,536,003CLINVAR
Cytogenetic Map2222q13.31CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14357416
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-09-22
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.