AutismKB 2.0

View CNVs/SVs


View by Evidence Type: Significant Enriched CNVs ( 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:All ( 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
AutCNV0000371 16 16q23.2 - - - CNVs Only Present In Patients; Significant Enriched CNVs; Zwaag, 2009
AutCNV0000372 16 16q23.2 - - - CNVs Only Present In Patients; Significant Enriched CNVs; Zwaag, 2009
AutCNV0000373 17 17p13.3 - - - CNVs Only Present In Patients; Significant Enriched CNVs; Zwaag, 2009
AutCNV0000374 17 17p11.2 - - - CNVs Only Present In Patients; Significant Enriched CNVs; Zwaag, 2009
AutCNV0000375 19 19p12 - - - CNVs Only Present In Patients; Significant Enriched CNVs; Zwaag, 2009
AutCNV0000376 19 19q13.2 - - - CNVs Only Present In Patients; Significant Enriched CNVs; Zwaag, 2009
AutCNV0000377 19 19q13.2 - - - CNVs Only Present In Patients; Significant Enriched CNVs; Zwaag, 2009
AutCNV0000378 19 19q13.2 - - - CNVs Only Present In Patients; Significant Enriched CNVs; Zwaag, 2009
AutCNV0000379 19 19q13.2 - - - CNVs Only Present In Patients; Significant Enriched CNVs; Zwaag, 2009
AutCNV0000380 19 19q13.42 - - - CNVs Only Present In Patients; Significant Enriched CNVs; Zwaag, 2009
AutCNV0000381 19 19q13.42 - - - CNVs Only Present In Patients; Significant Enriched CNVs; Zwaag, 2009
AutCNV0000382 22 22q12.3 - - - CNVs Only Present In Patients; Significant Enriched CNVs; Zwaag, 2009
AutCNV0000383 22 22q13.2 - - - CNVs Only Present In Patients; Significant Enriched CNVs; Zwaag, 2009
AutCNV0000384 22 22q13.2 - - - CNVs Only Present In Patients; Significant Enriched CNVs; Zwaag, 2009
AutCNV0000385 22 22q13.33 - - - CNVs Only Present In Patients; Significant Enriched CNVs; Zwaag, 2009
AutCNV0000386 22 22q13.33 - - - CNVs Only Present In Patients; Significant Enriched CNVs; Zwaag, 2009
AutCNV0000388 8 8p23.1 loss 12 8 Overlapping/Recurrent CNVs; Significant Enriched CNVs; Cho, 2009
AutCNV0000389 17 17p11.2 loss 4 0 Overlapping/Recurrent CNVs; Significant Enriched CNVs; Cho, 2009
AutCNV0004962 22 22q11.22 loss 130 0 CNVs Only Present In Patients; Significant Enriched CNVs; Hadley D, 2014
AutCNV0004963 5 5q11.1 loss 70 8 CNVs Only Present In Patients; Significant Enriched CNVs; Hadley D, 2014
AutCNV0004964 15 15q12 gain 28 0 CNVs Only Present In Patients; Significant Enriched CNVs; Hadley D, 2014
AutCNV0004965 15 15q12 gain 27 1 CNVs Only Present In Patients; Significant Enriched CNVs; Hadley D, 2014
AutCNV0004966 15 15q13.1 gain 24 0 CNVs Only Present In Patients; Significant Enriched CNVs; Hadley D, 2014
AutCNV0004973 1 1q21.1 - - - CNVs Only Present In Patients; Significant Enriched CNVs; de novo CNVs; Sanders SJ, 2015
AutCNV0004976 7 7q11.23 - - - CNVs Only Present In Patients; Significant Enriched CNVs; de novo CNVs; Sanders SJ, 2015

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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