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Variant : CV439773 (GRCh37/hg19 15q13.2-13.3(chr15:31140606-32438944)x1) Homo sapiens

Symbol: CV439773
Name: GRCh37/hg19 15q13.2-13.3(chr15:31140606-32438944)x1
Condition: See cases [RCV000515560]
Clinical Significance: pathogenic
Last Evaluated: 04/19/2017
Review Status: no assertion criteria provided
Related Genes: CHRNA7   FAN1   KLF13   MIR211   MTMR10   OTUD7A   TRPM1  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
HGVS Name(s): NC_000015.9:g.(?_31140606)_(32438944_?)del
Human AssemblyChrPosition (strand)Source
GRCh371531,140,606 - 32,438,944CLINVAR
Cytogenetic Map1515q13.2-13.3CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 13462282
Created: 2017-12-12
Species: Homo sapiens
Last Modified: 2019-08-06
Status: ACTIVE


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