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Variant : CV555360 (GRCh37/hg19 15q13.1-13.3(chr15:29382884-32192467)x1) Homo sapiens

Symbol: CV555360
Name: GRCh37/hg19 15q13.1-13.3(chr15:29382884-32192467)x1
Condition: not provided [RCV000683665]
Clinical Significance: pathogenic
Last Evaluated: 08/31/2017
Review Status: no assertion criteria provided
Related Genes: APBA2   ARHGAP11B   CHRFAM7A   FAM189A1   FAN1   GOLGA8H   GOLGA8J   KLF13   MIR211   MTMR10   NSMCE3   OTUD7A   TJP1   TRPM1  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh371529,382,884 - 32,192,467CLINVAR
Cytogenetic Map1515q13.1-13.3CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 13797405
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2019-10-01
Status: ACTIVE


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