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Variant : CV676710 (GRCh37/hg19 7q33(chr7:134648448-137942208)x1) Homo sapiens

Symbol: CV676710
Name: GRCh37/hg19 7q33(chr7:134648448-137942208)x1
Condition: not provided [RCV000849809]
Clinical Significance: uncertain significance
Last Evaluated: 03/14/2018
Review Status: no assertion criteria provided
Related Genes: AGBL3   AKR1D1   CALD1   CHRM2   CNOT4   CREB3L2   CYREN   DGKI   FAM180A   LUZP6   MTPN   NUP205   PTN   SLC13A4   STMP1   STRA8   TMEM140   WDR91  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh377134,648,448 - 137,942,208CLINVAR
Cytogenetic Map77q33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14981304
Created: 2019-10-08
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.