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Searched: Renal Cancer Sequencing Panel with CNV Detection
Search Results
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…variants (CNVs). This panel will detect all these variant types. Notably, the vast majority of CNVs, including 16p11.2 deletion syndrome and Smith-Magenis syndrome (17p11.2) will be detected. This panel is not designed to diagnose Prader…
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Test CodeMethodPrice1331Sequencing with CNV PG-Select$990
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Test CodeMethodPrice7647Sequencing with CNV PG-Select$990
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Test CodeMethodPrice10449Sequencing with CNV PG-Select$990
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Test CodeMethodPrice11551Sequencing with CNV PGxome$990493Sanger Sequencing$780
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Test CodeMethodPrice5471Sequencing with CNV PG-Select$1290
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Test CodeMethodPrice10159Sequencing with CNV PGxome$990
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…Cancer Genetics Our robust cancer genetic test menu offers genetic testing for various forms of tumors, cancers and syndromes. Earlier detection of tumors may lead to better outcomes (Coury et al. 2018. PubMed ID: 29750288) and genetic…
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Test CodeMethodPrice5467Sequencing with CNV PG-Select$990
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Test CodeMethodPrice7973Sequencing with CNV PG-Select$990
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Test CodeMethodPrice5459Sequencing with CNV PG-Select$990
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Test CodeMethodPrice5461Sequencing with CNV PG-Select$990
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Test CodeMethodPrice8409Sequencing with CNV PG-Select$990
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Test CodeMethodPrice3207Sequencing with CNV PG-Select$990
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Test CodeMethodPrice5457Sequencing with CNV PG-Select$990
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Test CodeMethodPrice5469Sequencing with CNV PG-Select$990
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Test CodeMethodPrice10151Sequencing with CNV PGxome$990
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Test CodeMethodPrice1685Sanger Sequencing$4909147Sequencing with CNV PGxome$990
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Test CodeMethodPrice15723Sequencing with CNV PG-Select$990
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Test CodeMethodPrice1464Sanger Sequencing$5808921Sequencing with CNV PGxome$990
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