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Clinical Diagnostics

Accelerate NGS variant interpretation with rapid search and insight into the full text of the genomic literature

Clinical Uses

Precision Therapeutics

Partner with us to gain a comprehensive view of the genetics of your disease of interest, from discovery to commercialization

Pharma Uses
A computer in a clinical lab using Mastermind genomic database software.

Software Solutions

Explore our platforms for germline and somatic variant interpretation


Access article information on more than 26 million variants, as well as curated germline variant content.

Meet Mastermind

Our Cancer Knowledgebase is used to interpret cancer variants, connecting them to therapies and clinical trials


Meet CKB

Services

Partner with our team of experts to create Tailored Solutions for your unique needs

Clinical Diagnostic Services
Precision Therapeutics Services

Data

Gain access to an expansive, constantly updated database of curated genomic information

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schedule a discovery call

Can I configure URLs so I don’t need to type?

Yes. URLs in Mastermind incorporate the search terms and Filter Categories, making it possible to pre-configure links by plugging in the values for gene, mutation, cnv, disease, hpo (phenotype), unii (therapy), cats (Filter Categories), and keyword (free-text terms).

https://mastermind.genomenon.com/detail?gene=brca1&mutation=brca1:C61G&cnv=del:17:42800000-52100000&disease=D001943&hpo=HP:0002664&unii=UNII:094ZI81Y45&cats=prognosis&cats=prognostic&keyword=trial&boolean=true&gene_op=and&mutation_op=and&cnv_op=and&disease_op=and&hpo_op=and&unii_op=and&keyword_op=and

Chromosome
GRCh37/hg19
GRCh38/hg38
1
NC_000001.10
NC_000001.11
2
NC_000002.11
NC_000002.12
3
NC_000003.11
NC_000003.12
4
NC_000004.11
NC_000004.12
5
NC_000005.9
NC_000005.10
6
NC_000006.11
NC_000006.12
7
NC_000007.13
NC_000007.14
8
NC_000008.10
NC_000008.11
9
NC_000009.11
NC_000009.12
10
NC_000010.10
NC_000010.11
11
NC_000011.9
NC_000011.10
12
NC_000012.11
NC_000012.12
13
NC_000013.10
NC_000013.11
14
NC_000014.8
NC_000014.9
15
NC_000015.9
NC_000015.10
16
NC_000016.9
NC_000016.10
17
NC_000017.10
NC_000017.11
18
NC_000018.9
NC_000018.10
19
NC_000019.9
NC_000019.10
20
NC_000020.10
NC_000020.11
21
NC_000021.8
NC_000021.9
22
NC_000022.10
NC_000022.11
X
NC_000023.10
NC_000023.11
Y
NC_000024.9
NC_000024.10

Learn more about how Genomenon is making genomic information actionable and supporting clinical diagnostic laboratories with patient diagnosis.

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