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Variant : CV154952 (GRCh38/hg38 7q11.23(chr7:73324677-73352304)x3) Homo sapiens

Symbol: CV154952
Name: GRCh38/hg38 7q11.23(chr7:73324677-73352304)x3
Condition: See cases [RCV000134603]
Clinical Significance: benign
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: FKBP6   TRIM50  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_73324677)_(73352304_?)dup
NC_000007.13:g.(?_72738675)_(72766313_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38773,324,677 - 73,352,304CLINVAR
GRCh37772,738,675 - 72,766,313CLINVAR
Build 36772,376,611 - 72,404,249CLINVAR
Cytogenetic Map77q11.23CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482183
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.