AutismKB 2.0

View CNVs/SVs


View by Evidence Type: All ( CNVs Only Present In Patients   de novo CNVs   Overlapping/Recurrent CNVs  
                                        CNVs Overlapping With ACRD   CNVs Not Present In Control   Significant Enriched CNVs   Others  All  )


View by Chromosome:13 ( 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 X  Y  All  )


Notes: ACRD: Autism Chromosome Rearrangement Database
CNV Name Chr Band Gain/Loss Number of CNVs Evidence Type Reference
Case Control
AutCNV0002822 13 13q31.1 loss 1 - Pinto, 2010
AutCNV0002823 13 13q31.1 loss 1 - Pinto, 2010
AutCNV0002824 13 13q31.1 loss 1 - Pinto, 2010
AutCNV0002825 13 13q31.1 loss 1 - Pinto, 2010
AutCNV0002826 13 13q31.2 gain 1 - Pinto, 2010
AutCNV0002827 13 13q31.3 gain 1 - Pinto, 2010
AutCNV0002828 13 13q31.3 loss 1 - Pinto, 2010
AutCNV0002829 13 13q32.1 gain 1 - Pinto, 2010
AutCNV0002830 13 13q32.1 gain 1 - Pinto, 2010
AutCNV0002831 13 13q32.2-32.3 gain 1 - Pinto, 2010
AutCNV0002832 13 13q33.2 loss 1 - Pinto, 2010
AutCNV0002833 13 13q33.2 gain 1 - Pinto, 2010
AutCNV0002834 13 13q34 gain 1 - Pinto, 2010
AutCNV0003107 13 13q34 gain 1 - Pinto, 2010
AutCNV0003352 13 13q13.3 gain 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003353 13 13q14.11 loss 2 - Overlapping/Recurrent CNVs; Gai, 2011
AutCNV0003354 13 13q21.1 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003355 13 13q21.31 gain 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003356 13 13q21.32 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003357 13 13q21.32 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003358 13 13q22.2 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003359 13 13q32.1 gain 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003360 13 13q34 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003361 13 13q34 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003683 13 13q11-12.11 loss 1 - CNVs Only Present In Patients; Gai, 2011

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  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018