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Variant : CV535443 (NC_000015.10:g.(?_30568981)_(32151126_?)del) Homo sapiens

Symbol: CV535443
Name: NC_000015.10:g.(?_30568981)_(32151126_?)del
Condition: Autistic disorder of childhood onset [RCV000754163]
Clinical Significance: pathogenic
Last Evaluated: 03/20/2018
Review Status: criteria provided, single submitter
Related Genes: ARHGAP11B   CHRNA7   FAN1   GOLGA8H   KLF13   LINC02352   MIR211   MTMR10   OTUD7A   TRPM1  
Variant Type: deletion (SO:0000159)
Evidence: research
HGVS Name(s): NC_000015.10:g.(?_30568981)_(32151126_?)del
Human AssemblyChrPosition (strand)Source
GRCh381530,568,981 - 32,151,126CLINVAR
Cytogenetic Map1515q13.2-13.3CLINVAR
Trait Synonyms: Autism

Disease Annotations
References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 14351715
Created: 2019-02-12
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.