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Comprehensive Leukemia Panel SNVs Small INDELs and CNVs

Original price was: $1,126.Current price is: $826.

-27%

The Comprehensive Leukemia Panel SNVs Small INDELs and CNVs is an advanced next-generation sequencing test that provides comprehensive genetic analysis for leukemia diagnosis and treatment planning. This cutting-edge test detects single nucleotide variants (SNVs), small insertions and deletions (INDELs), and copy number variations (CNVs) associated with various leukemia types. Priced at $826 USD, this comprehensive panel helps hematologists identify specific genetic mutations driving leukemia progression, enabling personalized treatment strategies and monitoring disease response. The test utilizes blood samples with a 2-3 week turnaround time, providing crucial genetic insights for patients with suspected or confirmed leukemia. By analyzing multiple genetic markers simultaneously, this panel offers a complete molecular profile essential for modern leukemia management and targeted therapy selection.

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Comprehensive Leukemia Panel SNVs Small INDELs and CNVs

Understanding Comprehensive Leukemia Genetic Testing

The Comprehensive Leukemia Panel SNVs Small INDELs and CNVs represents a revolutionary advancement in hematological cancer diagnostics. This sophisticated next-generation sequencing (NGS) test provides an exhaustive genetic analysis specifically designed for leukemia patients, offering unprecedented insights into the molecular drivers of disease progression and treatment response.

Leukemia, as a complex hematological malignancy, requires precise genetic characterization for optimal clinical management. Our comprehensive panel bridges the gap between traditional diagnostic methods and modern precision medicine, enabling healthcare providers to make informed decisions based on comprehensive genetic data.

What This Test Measures and Detects

This advanced genetic panel employs cutting-edge NGS technology to simultaneously analyze three critical types of genetic alterations:

Single Nucleotide Variants (SNVs)

  • Identifies point mutations in key leukemia-associated genes
  • Detects driver mutations affecting treatment response
  • Monitors emerging resistance mutations during therapy

Small Insertions and Deletions (INDELs)

  • Captures small genetic insertions and deletions
  • Identifies frameshift mutations affecting protein function
  • Detects critical mutations in tumor suppressor genes

Copy Number Variations (CNVs)

  • Analyzes gene amplification and deletion events
  • Identifies chromosomal abnormalities common in leukemia
  • Detects large-scale genetic rearrangements

Who Should Consider This Test

This comprehensive leukemia panel is recommended for individuals experiencing:

  • Unexplained fatigue, weakness, or persistent tiredness
  • Frequent infections or unusual bruising/bleeding
  • Unexplained weight loss or night sweats
  • Bone pain or joint discomfort
  • Enlarged lymph nodes, spleen, or liver
  • Abnormal complete blood count (CBC) results
  • Newly diagnosed leukemia patients seeking comprehensive genetic profiling
  • Patients with relapsed or refractory leukemia
  • Individuals requiring treatment response monitoring

Benefits of Comprehensive Leukemia Genetic Testing

Precision Diagnosis

Our panel provides definitive genetic characterization, enabling accurate leukemia subtyping and prognosis assessment. The comprehensive nature of this test ensures no critical genetic information is overlooked.

Personalized Treatment Planning

By identifying specific genetic mutations, hematologists can select targeted therapies with higher efficacy and reduced side effects. This precision approach maximizes treatment success while minimizing unnecessary interventions.

Disease Monitoring and Prognosis

The genetic profile obtained serves as a baseline for monitoring treatment response and detecting minimal residual disease. This enables early intervention when treatment adjustments are needed.

Family Risk Assessment

Identifies inherited genetic predispositions, allowing for appropriate genetic counseling and family risk assessment when applicable.

Understanding Your Test Results

Positive Results

A positive result indicates the presence of specific genetic alterations associated with leukemia. Your hematologist will interpret these findings in the context of your clinical presentation and develop a personalized treatment strategy.

Negative Results

A negative result suggests that no significant leukemia-associated genetic alterations were detected using current testing methods. However, clinical correlation with other diagnostic findings remains essential.

Variant of Uncertain Significance (VUS)

Some genetic changes may be classified as VUS, meaning their clinical significance is currently unknown. These findings require careful interpretation by your healthcare team and may warrant additional testing or monitoring.

Test Pricing Information

Test Component Price (USD)
Discount Price $826
Regular Price $1,126

Nationwide Availability

We have diagnostic centers conveniently located across the United States, serving patients in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, and many other cities. Our nationwide network ensures accessible, high-quality genetic testing services for leukemia patients throughout the country.

Take the Next Step Toward Precision Care

Don’t leave your leukemia diagnosis and treatment to chance. Our Comprehensive Leukemia Panel provides the genetic insights necessary for optimal care. With a turnaround time of 2-3 weeks and requiring only a simple blood sample, this test offers comprehensive genetic analysis without unnecessary delays.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your Comprehensive Leukemia Panel SNVs Small INDELs and CNVs test. Our genetic specialists are ready to assist you in taking control of your leukemia management through advanced genetic testing.

Experience the power of precision medicine with our state-of-the-art leukemia genetic panel. Book your test today and gain the genetic insights needed for personalized leukemia care.