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Variant : CV167011 (NR_037472.1(MIR3910-1):n.-2474_315del) Homo sapiens

Symbol: CV167011
Name: NR_037472.1(MIR3910-1):n.-2474_315del
Condition: Normal pregnancy [RCV000161577]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: MIR3910-1   MIR3910-2  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: case-control
HGVS Name(s): NC_000009.12:g.91633777_91636565del
NC_000009.11:g.94396059_94398847del
Position
Human AssemblyChrPosition (strand)Source
GRCh38991,633,777 - 91,636,565CLINVAR
GRCh37994,396,059 - 94,398,847CLINVAR
Cytogenetic Map99q22.31CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9831836
Created: 2015-03-10
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.