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Searched: Familial Hypercholesterolemia 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 CodeMethodPrice10163Sequencing with CNV PGxome$990
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Test CodeMethodPrice870Sanger Sequencing$9409889Sequencing with CNV PGxome$990
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Test CodeMethodPrice12035Sequencing with CNV PGxome$990871Sanger Sequencing$1060
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Test CodeMethodPrice10699Sequencing with CNV PGxome$9902818Sanger Sequencing$780
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Test CodeMethodPrice12033Sequencing with CNV PGxome$990872Sanger Sequencing$1340
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…(FHL5) via the STXBP2 Gene Test Code Method Price 11723 Sequencing with CNV PGxome $990 214 Sanger Sequencing $960 Familial Hypercholesterolemia (FH) Panel Test Code Method Price 10163 Sequencing with CNV PGxome $990 Familial…
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…Test Code Method Price 11723 Sequencing with CNV PGxome $990 214 Sanger Sequencing $960 Familial Hypercholesterolemia (FH) Panel Test Code Method Price 10163 Sequencing with CNV PGxome $990 Familial Hypercholesterolemia…
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…$990 Familial Hemophagocytic Lymphohistiocytosis (FHL) Panel Test Code Method Price 10377 Sequencing with CNV PGxome $990 Familial Hypercholesterolemia (FH) Panel Test Code Method Price 10163 Sequencing with CNV PGxome $990 Familial…
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…$990 Familial Hemophagocytic Lymphohistiocytosis (FHL) Panel Test Code Method Price 10377 Sequencing with CNV PGxome $990 Familial Hypercholesterolemia (FH) Panel Test Code Method Price 10163 Sequencing with CNV PGxome $990 Familial…
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Test CodeMethodPrice13025Sequencing with CNV PGxome$990
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…Dr. Diane Allingham-Hawkins, Ph.D, FCCMG, FACM, the Senior Laboratory Director & Dean of Geneticists at PreventionGenetics presents "Getting More From Your Sequencing Test Copy Number Variant Detection by Next Generation Sequencing…
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Test CodeMethodPrice3409Sequencing with CNV PG-Select$990
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Test CodeMethodPrice2663Sequencing with CNV PGxome$1290
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…and panels for fertility or infertility issues, obesity, diabetes and more. Accurate genetic testing is imperative for diagnostics and can help make informed treatment decisions. CMA Aldosteronism Ambiguous Genitalia Bone Fragility Combined…
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Test CodeMethodPrice7045Sequencing with CNV PG-Select$990
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Test CodeMethodPrice12605Sequencing with CNV PGxome$990
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Test CodeMethodPrice10125Sequencing with CNV PGxome$990
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Test CodeMethodPrice10323Sequencing with CNV PGxome$990
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Test CodeMethodPrice10377Sequencing with CNV PGxome$990
RESULTS KEY
- Tests & Panels
- Categories
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- Pages & Documents
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