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Variant : CV162556 (GRCh38/hg38 7q11.23(chr7:74068087-75068321)x3) Homo sapiens

Symbol: CV162556
Name: GRCh38/hg38 7q11.23(chr7:74068087-75068321)x3
Condition: See cases [RCV000141316]
Clinical Significance: likely benign
Last Evaluated: 09/09/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CASTOR2   CLIP2   EIF4H   ELN   GTF2I   GTF2IRD1   GTF2IRD2   LAT2   LIMK1   MIR10525   MIR590   NCF1   RCC1L   RFC2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(74053426_74068087)_(75068321_75069953)dup
NC_000007.13:g.(73467756_73482417)_(74481540_74485767)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38774,068,087 - 75,068,321CLINVAR
GRCh37773,482,417 - 74,481,540CLINVAR
Build 36773,120,353 - 74,119,476CLINVAR
Cytogenetic Map77q11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489980
Created: 2014-09-09
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.