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New filters have been added to narrow your search: Test target, to filter by number of genes; Genes and Conditions, to search by gene symbol or condition name; and Labs, to search by a laboratory name.
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GeneThis summary box displays a gene, condition, or laboratory matching your search query. | H19-H19 imprinted maternally expressed transcript |
| Also know as: ASM, ASM1, BWS, D11S813E, GMRSP, LINC00008, MIR675HG, NCRNA00008, WT2; GeneID:283120; Location:11p15.5; | |
| Associated condition: Wilms tumor 1 |
Labs matching your search
11 labs with tests matching your search, 1 lab matching in other ways
| Lab name | Tests matching your search |
|---|---|
| Amsterdam UMC Genome Diagnostics Netherlands | 3 |
| CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 |
| DNA Labs India India | 1 |
| Fulgent Genetics United States | 1 |
| Genome Diagnostics Laboratory Canada | 2 |
| Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 10 |
| PreventionGenetics, part of Exact Sciences United States | 1 |
| Quantitative Genomic Medicine Laboratories, SL Spain | 1 |
| Shodair Medical Genetics Laboratory United States | 2 |
| Tempus AI - CHI United States | 1 |
| Tempus AI - RTP United States | 1 |
| AiLife Diagnostics United States | 0 |
Results:
24 genetic tests from 11 labs with tests matching your search, 1 lab matching in other ways
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods | |
|---|---|---|---|---|
| 2 | 3 |
| ||
| 1 | 4 |
| ||
| 2 | 647 |
| ||
| 1 | 1 |
| ||
| 2 | 647 |
| ||
| 1 | 1 |
| ||
Beckwith-Wiedemann syndrome, 130650, Autosomal dominant (Beckwith-Wiedemann syndrome) (MLPA) | 1 | 1 |
| |
| 1 | 1 |
| ||
| 1 | 1 |
| ||
Silver-Russell syndrome, 180860, Isolated cases; SRS (Silver-Russell syndrome) (MLPA) | 1 | 1 |
| |
Silver-Russell syndrome, 180860, Isolated cases; SRS (Silver-Russell syndrome) (Prenatal) (MLPA) | 1 | 1 |
| |
| 1 | 1 |
| ||
| 1 | 1 |
| ||
| 1 | 1 |
| ||
| 1 | 1 |
| ||
| 3 | 1969 |
| ||
| 2 | 2 |
| ||
| 1 | 10 |
| ||
| 3 | 571 |
| ||
| 4 | 6 |
|
24 tests from 11 labs
Page 1 of 2❯Russell-Silver Syndrome by Shodair Medical Genetics Laboratory, Shodair Children's Hospital
2 conditions, 3 genes
2 conditions, 3 genes
Beckwith-Wiedemann Syndrome by Shodair Medical Genetics Laboratory, Shodair Children's Hospital
1 condition, 4 genes
1 condition, 4 genes
Tempus xT by Tempus AI - RTP
2 conditions, 647 genes
2 conditions, 647 genes
Tempus xT by Tempus AI - CHI
2 conditions, 647 genes
2 conditions, 647 genes
Beckwith-Wiedemann syndrome, 130650, Autosomal dominant (Beckwith-Wiedemann syndrome) (H19 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Beckwith-Wiedemann syndrome, 130650, Autosomal dominant (Beckwith-Wiedemann syndrome) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Beckwith-Wiedemann syndrome, 130650, Autosomal dominant (Beckwith-Wiedemann syndrome) (H19 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Beckwith-Wiedemann syndrome, 130650, Autosomal dominant (Beckwith-Wiedemann syndrome) (Prenatal) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Silver-Russell syndrome, 180860, Isolated cases; SRS (Silver-Russell syndrome) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Silver-Russell syndrome, 180860, Isolated cases; SRS (Silver-Russell syndrome) (Prenatal) (MLPA) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Silver-Russell syndrome, 180860, Isolated cases; SRS (Silver-Russell syndrome) (H19 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Silver-Russell syndrome, 180860, Isolated cases; SRS (Silver-Russell syndrome) (H19 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Wilms tumor 2, 194071, Autosomal dominant, Somatic mutation; WT2 (Nephroblastoma) (H19 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Wilms tumor 2, 194071, Autosomal dominant, Somatic mutation; WT2 (Nephroblastoma) (H19 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
qGenEx Intellectual disability by Quantitative Genomic Medicine Laboratories, SL
3 conditions, 1969 genes
3 conditions, 1969 genes
Methylation Chr.11p15 (KCNQ1OT1 & H19) by Amsterdam UMC Genome Diagnostics, Amsterdam University Medical Center
2 conditions, 2 genes
2 conditions, 2 genes
Multi Locus Imprinting Disorders (MLIPD) by Amsterdam UMC Genome Diagnostics, Amsterdam University Medical Center
1 condition, 10 genes
1 condition, 10 genes
NGS Skeletal Dysplasia by Amsterdam UMC Genome Diagnostics, Amsterdam University Medical Center
3 conditions, 571 genes
3 conditions, 571 genes
Wilms tumor: Full gene sequencing panel by CEN4GEN Institute for Genomics and Molecular Diagnostics
4 conditions, 6 genes
4 conditions, 6 genes
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