If a variant has more than one submission, it may be counted in more than one significance column. If this is the
case, the total number of variants will be less than the sum of the other cells.
pathogenic |
likely pathogenic |
uncertain significance |
likely benign |
benign |
total |
2
|
0 |
673
|
414
|
89
|
1144
|
Gene and significance breakdown #
Total genes and gene combinations: 2
Submitter and significance breakdown #
Submitter |
pathogenic |
uncertain significance |
likely benign |
benign |
total |
Invitae
|
0 |
650
|
386
|
84
|
1120
|
Fulgent Genetics, Fulgent Genetics
|
0 |
106
|
19
|
2
|
127
|
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories
|
0 |
5
|
13
|
21
|
39
|
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen
|
0 |
4
|
24
|
9
|
37
|
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center
|
0 |
1
|
6
|
11
|
18
|
Genome-Nilou Lab
|
0 |
0 |
0 |
12
|
12
|
Genome Diagnostics Laboratory, University Medical Center Utrecht
|
0 |
1
|
1
|
6
|
8
|
Revvity Omics, Revvity Omics
|
0 |
6
|
0 |
0 |
6
|
Neuberg Supratech Reference Laboratories Pvt Ltd, Neuberg Centre for Genomic Medicine
|
0 |
4
|
0 |
0 |
4
|
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute
|
0 |
3
|
0 |
0 |
3
|
Centre for Mendelian Genomics, University Medical Centre Ljubljana
|
0 |
3
|
0 |
0 |
3
|
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago
|
0 |
3
|
0 |
0 |
3
|
OMIM
|
2
|
0 |
0 |
0 |
2
|
Baylor Genetics
|
0 |
2
|
0 |
0 |
2
|
Institute of Human Genetics, University of Leipzig Medical Center
|
0 |
1
|
0 |
1
|
2
|
Mendelics
|
0 |
0 |
0 |
1
|
1
|
Genomic Research Center, Shahid Beheshti University of Medical Sciences
|
0 |
1
|
0 |
0 |
1
|
Phosphorus, Inc.
|
0 |
1
|
0 |
0 |
1
|
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