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Variant : CV162003 (GRCh38/hg38 7p21.2(chr7:15533812-15855669)x1) Homo sapiens

Symbol: CV162003
Name: GRCh38/hg38 7p21.2(chr7:15533812-15855669)x1
Condition: See cases [RCV000140844]
Clinical Significance: likely benign|uncertain significance
Last Evaluated: 04/04/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AGMO   LINC02587   MEOX2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_15533812)_(15855669_?)del
NC_000007.13:g.(?_15573437)_(15895294_?)del
NC_000007.12:g.(?_15539962)_(15861819_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38715,533,812 - 15,855,669CLINVAR
GRCh37715,573,437 - 15,895,294CLINVAR
Build 36715,539,962 - 15,861,819CLINVAR
Cytogenetic Map77p21.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9488372
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.