Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV676360 (GRCh37/hg19 16p13.3(chr16:3469027-4328143)x3) Homo sapiens

Symbol: CV676360
Name: GRCh37/hg19 16p13.3(chr16:3469027-4328143)x3
Condition: not provided [RCV000849459]
Clinical Significance: pathogenic
Last Evaluated: 03/08/2018
Review Status: no assertion criteria provided
Related Genes: ADCY9   C16orf90   CLUAP1   CREBBP   DNASE1   NAA60   NLRC3   SLX4   SRL   TFAP4   TRAP1   ZNF597  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37163,469,027 - 4,328,143CLINVAR
Cytogenetic Map1616p13.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14980972
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-01-07
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.