Search Results for 'variant points'

variant points published presentations and documents on DocSlides.

ClinGen Sequence Variant Interpretation Recommendation for de novo Cri
ClinGen Sequence Variant Interpretation Recommendation for de novo Cri
by holly
-Version 11 Working Group Pagehttps//clinicalgenom...
BioCuration  Call: Sequence Variant Interpretation WG Update
BioCuration Call: Sequence Variant Interpretation WG Update
by Littlespud
Steven Harrison (. sharrison@bwh.harvard.edu. ). M...
Case Z arr [GRCh37] 19p13.11(18291753_18311626) x3
Case Z arr [GRCh37] 19p13.11(18291753_18311626) x3
by berey
2-month-old female with Tetralogy of Fallot; inher...
Case P arr [GRCh37] 17q21.2
Case P arr [GRCh37] 17q21.2
by Princecharming
(39529437_39545915) x3 mat. 10-year-old female wit...
CNV J arr [GRCh37] 3q28 (190380498_191783134)x1
CNV J arr [GRCh37] 3q28 (190380498_191783134)x1
by alyssa
No phenotype or inheritance information provided. ...
Case E arr [GRCh37] 15q13.2
Case E arr [GRCh37] 15q13.2
by miller
(30507853_30807921) x1 pat. 6 month old male with ...
Case T arr [GRCh37] 1q22
Case T arr [GRCh37] 1q22
by ceila
(155887333_156224120) x3. Newborn with unspecified...
Case S arr [GRCh37] 3q26.32
Case S arr [GRCh37] 3q26.32
by paisley
(175816894_177834521)x3 mat. 6-year-old male with ...
Hearing Loss  CDWG Curation
Hearing Loss CDWG Curation
by leah
Update. Biocurator. Call. 5.11.17. Marina DiStefa...
Case F arr [GRCh37] 1p36.33
Case F arr [GRCh37] 1p36.33
by harmony
(1379519_1435227)x1. 2-month-old female with unila...
Case N arr [GRCh37] 10q22.2
Case N arr [GRCh37] 10q22.2
by blanko
(76738122-76743018) x3 . 4 year old female with de...
Case B arr [GRCh37] 11p11.2 (45904399_46480747) x 1 (
Case B arr [GRCh37] 11p11.2 (45904399_46480747) x 1 (
by ivy
dn. ). 5-year-old female with developmental delay;...
ClinGen RASopathy EP Gene Curation
ClinGen RASopathy EP Gene Curation
by morton
Biocurator Working Group Presentation. 5.10.2018. ...