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Variant : CV674978 (GRCh37/hg19 12p13.31(chr12:6070459-6737675)x3) Homo sapiens

Symbol: CV674978
Name: GRCh37/hg19 12p13.31(chr12:6070459-6737675)x3
Condition: not provided [RCV000848085]
Clinical Significance: uncertain significance
Last Evaluated: 04/17/2017
Review Status: no assertion criteria provided
Related Genes: CD27   CD9   CHD4   GAPDH   IFFO1   LPAR5   LTBR   MRPL51   NCAPD2   NOP2   PLEKHG6   SCNN1A   TAPBPL   TNFRSF1A   VAMP1   VWF  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37126,070,459 - 6,737,675CLINVAR
Cytogenetic Map1212p13.31CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14979651
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-03-31
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.