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Variant : CV383125 (GRCh37/hg19 13q33.2-34(chr13:106941499-113674752)x3) Homo sapiens

Symbol: CV383125
Name: GRCh37/hg19 13q33.2-34(chr13:106941499-113674752)x3
Condition: See cases [RCV000447024]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ABHD13   ANKRD10   ANKRD10-IT1   ARGLU1   ARHGEF7   ATP11A   ATP11AUN   CARS2   COL4A1   COL4A2   EFNB2   FAM155A   ING1   IRS2   LIG4   LINC00567   MCF2L   MYO16   NAXD   RAB20   SOX1   SPACA7   TEX29   TNFSF13B   TUBGCP3  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3713106,941,499 - 113,674,752CLINVAR
Cytogenetic Map1313q33.2-34CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 12851744
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-01-07
Status: ACTIVE


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