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

Variant : CV554965 (GRCh37/hg19 10p13(chr10:12802555-14847149)x1) Homo sapiens

Symbol: CV554965
Name: GRCh37/hg19 10p13(chr10:12802555-14847149)x1
Condition: not provided [RCV000683270]
Clinical Significance: uncertain significance
Last Evaluated: 01/23/2018
Review Status: no assertion criteria provided
Related Genes: BEND7   CAMK1D   CCDC3   FAM107B   FRMD4A   MCM10   OPTN   PHYH   PRPF18   SEPHS1   UCMA  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371012,802,555 - 14,847,149CLINVAR
Cytogenetic Map1010p13CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13796315
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-11-17
Status: ACTIVE



NHLBI Logo

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