Clinical Genomics Laboratory (Laboratory for Precision Diagnostics, University of Washington)
General information
Clinical Genomics Laboratory
Laboratory for Precision Diagnostics, University of Washington
1959 NE Pacific St., HSB H-561
Seattle
Washington
United States - 98195
http://uwcpdx.org/clinical-genomics-laboratory/
Organization ID: 505820
Laboratory for Precision Diagnostics, University of Washington
1959 NE Pacific St., HSB H-561
Seattle
Washington
United States - 98195
http://uwcpdx.org/clinical-genomics-laboratory/
Organization ID: 505820
Assertion criteria
Level: Assertion criteria provided
Summary of submissions to ClinVar
Total submissions: 368
Gene
Gene | Submissions | Last Updated |
---|---|---|
ASTN2 | 1 | Nov 15, 2018 |
AUTS2 | 1 | Aug 2, 2017 |
CNTN4 | 2 | Mar 19, 2020 |
CREBBP | 1 | Mar 29, 2017 |
CSMD1 | 1 | Aug 2, 2017 |
EYA1 | 1 | Mar 29, 2017 |
FAF1 | 1 | May 8, 2019 |
FOXP1 | 1 | Aug 2, 2017 |
GPC5 | 1 | Jan 22, 2016 |
LRP1B | 1 | May 8, 2019 |
MARCHF1 | 1 | Apr 4, 2016 |
MBD5 | 1 | Jan 26, 2018 |
MED13L | 1 | Nov 15, 2018 |
NR2F2 | 1 | Aug 2, 2017 |
NR3C2 | 1 | Jan 22, 2016 |
NRG3 | 1 | Apr 4, 2016 |
PPP3CA | 1 | May 8, 2019 |
PRICKLE1 | 1 | Mar 19, 2020 |
PRKN | 2 | Nov 22, 2017 |
PTPRN2 | 1 | May 8, 2019 |
SLC3A1 | 1 | Apr 4, 2016 |
TCF12 | 1 | May 8, 2019 |
Condition
Name | Submissions | Last Updated |
---|---|---|
See cases | 364 | May 18, 2021 |
not provided | 2 | Apr 4, 2016 |
not specified | 2 | Apr 4, 2016 |
Testing in GTR
Disease name | Number of tests |
---|---|
4p partial monosomy syndrome | 1 test |
5p partial monosomy syndrome | 1 test |
7q11.23 microduplication syndrome | 1 test |
Acute lymphoid leukemia | 2 tests |
Acute myeloid leukemia | 2 tests |
Advanced maternal age gravida | 1 test |
Angelman syndrome | 1 test |
Autism spectrum disorder | 1 test |
B-cell chronic lymphocytic leukemia | 2 tests |
B-cell non-Hodgkin lymphoma | 2 tests |
Chromophobe renal cell carcinoma | 1 test |
Chromosome 15q11.2 duplication syndrome | 1 test |
Chromosome 1p36 deletion syndrome | 1 test |
Chromosome 22q11.2 deletion syndrome, distal | 1 test |
Chromosome 22q11.2 microduplication syndrome | 1 test |
Clear cell carcinoma of kidney | 1 test |
Cognitive impairment | 1 test |
Congenital chromosomal disease | 1 test |
Dysmorphic features | 1 test |
Glioblastoma | 2 tests |
Hematologic neoplasm | 1 test |
Hypogonadism with anosmia | 1 test |
Infertility disorder | 1 test |
Infertility due to oligospermia | 1 test |
Intellectual disability | 1 test |
Known OR suspected fetal abnormality affecting management of mother | 1 test |
Lung carcinoma | 1 test |
Lymphoid leukemia | 1 test |
Lymphoma | 2 tests |
Male infertility | 1 test |
Maternal care for suspected chromosomal abnormality in fetus | 1 test |
Miller Dieker syndrome | 1 test |
Miscarriage | 1 test |
Multiple congenital anomalies | 2 tests |
Multiple myeloma | 3 tests |
Myelodysplastic syndrome | 2 tests |
Myeloid leukemia | 1 test |
Nonpapillary renal cell carcinoma | 1 test |
Pallister-Killian syndrome | 1 test |
Papillary renal cell carcinoma | 1 test |
Plasma cell neoplasm | 1 test |
Potocki-Lupski syndrome | 1 test |
Prader-Willi syndrome | 1 test |
Renal cell carcinoma | 2 tests |
Sarcoma | 2 tests |
Smith-Magenis syndrome | 1 test |
Solid tumor | 3 tests |
Velocardiofacial syndrome | 1 test |
Williams syndrome | 1 test |
X-linked ichthyosis with steryl-sulfatase deficiency | 1 test |
Y chromosome deletions | 1 test |
Y chromosome-related disorders | 1 test |