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Variant : CV165415 (GRCh38/hg38 7q31.1(chr7:113245819-114828815)x3) Homo sapiens

Symbol: CV165415
Name: GRCh38/hg38 7q31.1(chr7:113245819-114828815)x3
Condition: See cases [RCV000143728]
Clinical Significance: uncertain significance
Last Evaluated: 03/10/2014
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: FOXP2   MIR3666   PPP1R3A  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_113245819)_(114828815_?)dup
NC_000007.13:g.(?_112885874)_(114468870_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh387113,245,819 - 114,828,815CLINVAR
GRCh377112,885,874 - 114,468,870CLINVAR
Build 367112,673,110 - 114,256,106CLINVAR
Cytogenetic Map77q31.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9491326
Created: 2014-09-09
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.