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:14 ( 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
AutCNV0002844 14 14q21.3 loss 1 - Pinto, 2010
AutCNV0002845 14 14q21.3 loss 1 - Pinto, 2010
AutCNV0002846 14 14q21.3 loss 1 - Pinto, 2010
AutCNV0002847 14 14q21.3 loss 1 - Pinto, 2010
AutCNV0002848 14 14q21.3 loss 1 - Pinto, 2010
AutCNV0002849 14 14q22.2 loss 1 - Pinto, 2010
AutCNV0002850 14 14q22.2 loss 1 - Pinto, 2010
AutCNV0002851 14 14q23.1 gain 1 - Pinto, 2010
AutCNV0002852 14 14q23.1 loss 1 - Pinto, 2010
AutCNV0002853 14 14q23.2 gain 1 - Pinto, 2010
AutCNV0002854 14 14q24.3 loss 1 - Pinto, 2010
AutCNV0002855 14 14q31.3 loss 1 - Pinto, 2010
AutCNV0002856 14 14q31.3 loss 1 - Pinto, 2010
AutCNV0002857 14 14q32.33 loss 1 - Pinto, 2010
AutCNV0003108 14 14q32.33 gain 1 - Pinto, 2010
AutCNV0003362 14 14q13.1 gain 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003363 14 14q13.2 loss 2 - Overlapping/Recurrent CNVs; Gai, 2011
AutCNV0003364 14 14q13.2 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003365 14 14q21.2-21.3 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003366 14 14q21.3 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003367 14 14q21.3 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003368 14 14q21.3 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003369 14 14q24.3-31.1 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003370 14 14q31.1-31.2 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003371 14 14q32.33 loss 1 - CNVs Only Present In Patients; Gai, 2011

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Simple Query:


  (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