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Variant : CV514196 (GRCh37/hg19 3q29(chr3:195457650-196263123)) Homo sapiens

Symbol: CV514196
Name: GRCh37/hg19 3q29(chr3:195457650-196263123)
Condition: Autistic disorder of childhood onset [RCV000626534]
Clinical Significance: uncertain significance
Last Evaluated: 01/01/2017
Review Status: criteria provided, single submitter
Related Genes: MUC20   MUC4   PCYT1A   RNF168   SLC51A   SMCO1   TCTEX1D2   TFRC   TM4SF19   TNK2   TNK2-AS1   UBXN7   ZDHHC19  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh373195,457,650 - 196,263,123CLINVAR
Cytogenetic Map33q29CLINVAR
Trait Synonyms: Attention deficit; Attention deficit disorder; Attention deficit hyperactivity disorder; Attention deficits; Childhood attention deficit/hyperactivity disorder; HYPERACTIVITY OF CHILDHOOD



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13611873
Created: 2018-06-12
Species: Homo sapiens
Last Modified: 2020-03-31
Status: ACTIVE



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