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Variant : CV165446 (GRCh37/hg19 7q34(chr7:141937588-142486548)x3) Homo sapiens

Symbol: CV165446
Name: GRCh37/hg19 7q34(chr7:141937588-142486548)x3
Condition: See cases [RCV000143759]
Clinical Significance: uncertain significance
Last Evaluated: 03/18/2014
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: MIR11400   MTRNR2L6   PRSS1   PRSS58   TRB   TRBV10-1   TRBV10-2   TRBV10-3   TRBV11-1   TRBV11-2   TRBV11-3   TRBV12-3   TRBV12-4   TRBV12-5   TRBV13   TRBV14   TRBV15   TRBV17   TRBV18   TRBV19   TRBV2   TRBV20-1   TRBV24-1   TRBV25-1   TRBV27   TRBV28   TRBV29-1   TRBV3-1   TRBV4-1   TRBV4-2   TRBV4-3   TRBV5-1   TRBV5-4   TRBV5-5   TRBV5-6   TRBV5-7   TRBV5-8   TRBV6-1   TRBV6-2   TRBV6-3   TRBV6-4   TRBV6-5   TRBV6-6   TRBV6-8   TRBV6-9   TRBV7-2   TRBV7-3   TRBV7-4   TRBV7-6   TRBV7-7   TRBV7-8   TRBV7-9   TRBV9  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.13:g.(?_141937588)_(142486548_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh377141,937,588 - 142,486,548CLINVAR
Build 367141,584,062 - 142,186,550CLINVAR
Cytogenetic Map77q34CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9491357
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-21
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.