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    v1.0.28
    OpenPayerNPI Medicare & MedicaidNPI 1073251336
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    NPI 1073251336 — Billing Profile & Reimbursement Data

    NPI 1073251336 · XX · healthcare

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    NPI 1073251336 is a healthcare provider located in Unspecified Location. This profile covers 25 Medicare and 0 Medicaid CPT/HCPCS procedure codes, with claims volume, average reimbursement, and total revenue by code, benchmarked against other providers billing the same services. Note: "XX" is a placeholder CMS uses when a provider's practice-location state wasn't reported — not a traditional US state; claims coded under it are grouped and benchmarked here the same way a traditional state would be.

    Provider details (source: NPPES NPI Registry)

    FieldValue
    Entity TypeIndividual
    OrganizationNPI 1073251336
    Address
    City
    StateXX (Unspecified Location)
    ZIP
    TaxonomyN/A
    NPI Enumerated
    NPI DeactivatedMarch 10, 2025

    (source: CMS Medicare & Medicaid claims data)

    Key Findings

    The provider’s Medicare billing is heavily concentrated in molecular and genetic diagnostic assays, with top revenue drivers including 81307 (2.9K claims, $663 avg paid/claim, $2M revenue (13.0%)), 81321 (3K claims, $588 avg paid/claim, $1.8M revenue (11.7%)), and 81249 (2.8K claims, $588 avg paid/claim, $1.6M revenue (10.9%)). This code mix — full-gene and targeted sequencing for BRCA2/PALB2, PTEN, and G6PD among others — is consistent with a specialized clinical or commercial genomics laboratory focused on hereditary disease and oncology testing rather than routine clinical pathology services.

    Revenue concentration is material: the precomputed top-3 codes account for 35.6% of this provider’s total Medicare revenue, against a lifetime Medicare revenue base of $15M. That level of concentration in a small set of genetic assays indicates the provider’s financial performance is meaningfully driven by demand and reimbursement dynamics for a narrow set of high-value tests.

    This provider is effectively single-payer in the available data: Medicare revenue is $15M while there is no Medicaid billing on file. The absence of Medicaid activity suggests limited exposure to state Medicaid programs in the dataset and means analyses of payer mix, Medicaid market share, or state-level Medicaid contracting are not possible from the billing record provided.

    Medicare: Total Revenue Breakdown by CPT/HCPCS Code

    Medicare revenue breakdown by CPT/HCPCS procedure code.

    View: Bar Chart1 / 2

    Medicare Revenue by CPT/HCPCS Code

    Medicare: Complete Services Breakdown

    The CPT/HCPCS codes generating the most Medicare revenue for this provider.

    25 rows

    CPT/HCPCS CodeDescriptionClaimsAvg PaidRevenue
    81307The lab analyst performs the technical lab test on a specimen such as blood, to analyze the entire gene sequence for the partner and localizer of BRCA2 (PALB2) gene.2,950$660$2M
    81321The lab analyst performs the technical lab test to analyze the entire gene sequence for the phosphatase and tensin homolog, or PTEN, gene.2,990$590$1.8M
    81249The lab analyst performs the technical lab test to analyze known the full gene sequence of the glucose–6–phosphate dehydrogenase (G6PD) gene.2,770$590$1.6M
    81238The lab analyst performs the technical lab test to analyze the full gene sequence of the coagulation factor IX (F9) gene.2,750$590$1.6M
    81223The lab analyst performs the technical lab test to analyze the entire gene sequence for cystic fibrosis transmembrane conductance regulator gene, also known as CFTR.2,770$490$1.4M
    81334The lab analyst performs the technical lab test to detect the presence of specific changes in the runt related transcription factor 1 (RUNX) gene for targeted sequence analysis, such as exons 3–8.2,860$320$923.5K
    81311The lab analyst performs the technical lab test to analyze variants in exon 2, such as codons 12 and 13, and exon 3, such as codon 61, for the neuroblastoma RAS viral, v–ras, oncogene homolog, also…2,860$290$829.1K
    81320The lab analyst performs the technical lab test to detect the presence of common changes in the phospholipase C gamma 2 gene (PLCG2).2,860$290$817.7K
    K1034Provision of covid-19 test, nonprescription self-administered and self-collected use, fda approved, authorized or cleared, one test count53,280$10$639.4K
    81279The lab analyst performs the technical lab test on a specimen such as blood to analyze specific gene sequences of the JAK2 (Janus kinase 2) gene, such as exons 12 and 13, which may be associated with…2,860$180$520.3K

    Showing 1–10 of 25

    Medicare: Competitive Analysis & Benchmarks

    How this provider's Medicare billing volume and revenue compare to other providers nationally and within its state, across 25 CPT/HCPCS codes. Note: this provider's state, "XX," is a placeholder CMS uses when a provider's practice-location state wasn't reported — not a traditional US state; the State panel below benchmarks against other providers coded under the same designation.

    View: State1 / 2

    Claims Volume vs. Unspecified Location Distribution
    NPI 1073251336 — 0 of 0 codes billed far more than typical (above p95)
    p5–p95 (all providers)p25–p75MedianThis providerOutlier
    Rank Distribution — Unspecified Location

    Full comparison — all codes billed, vs. state median

    25 rows

    CPT/HCPCS CodeRankProvider CountMedian ClaimsAvg PaidAverage Revenue
    8116260N/A$N/A$N/A
    8120150N/A$N/A$N/A
    8120920N/A$N/A$N/A
    8121610N/A$N/A$N/A
    8122320N/A$N/A$N/A
    8123820N/A$N/A$N/A
    8124120N/A$N/A$N/A
    8124220N/A$N/A$N/A
    8124920N/A$N/A$N/A
    8125010N/A$N/A$N/A

    Showing 1–10 of 25

    Frequently Asked Questions

    References

    1. 1.Medicare Physician & Other Practitioner by Provider and Service. CMS.gov.Provider-level Medicare Part B utilization and payment data.
    2. 2.NPPES NPI Registry. CMS.gov.National Provider Identifier registry used for provider enumeration and taxonomy metadata.

    Trek Health ingests and normalizes Transparency in Coverage data and payer policy updates to give provider organizations a clear view of how commercial reimbursement behaves across markets, payers, and services. Our platform transforms raw payer disclosures into structured intelligence that supports contract evaluation, payer negotiations, and service line strategy. By combining market benchmarks with ongoing policy visibility, Trek helps teams identify variability, risk, and opportunity in commercial reimbursement. The result is faster insight, stronger negotiating positions, and more informed financial decisions.

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    Lifetime revenue by payer source
    Payer SourceTotal Paid
    Medicare$15M
    Medicaid$0

    The provider shows a strong national competitive standing on many top assays: 81307 ranks #3 of 62 providers nationally (97th percentile), 81321 ranks #3 of 37 (94th percentile), and 81249 ranks #4 of 62 (95th percentile). Multiple other codes also appear at high national percentiles, indicating this entity is a major national performer or capacity node for a broad set of genetic tests rather than a low-volume local lab.

    Several individual codes are flagged as statistical outliers or notably above typical national volume, highlighting exceptional volume for particular assays. For example, 81279 is described as an "extreme outlier, far above typical national volume" (2.9K claims, $182 avg paid/claim, $520.3K revenue (3.5%)), while many assays such as 81307, 81321, 81249, 81238, and 81223 are noted as "notably above typical national volume," reinforcing that this provider’s activity is unusually concentrated in genetic testing.

    A distinct high-volume, low-revenue line appears in COVID test provisioning via K1034: 53.3K claims, $12 avg paid/claim, $639.4K revenue (4.3%), with a national rank of #205 of 30143 providers and described as "typical, unremarkable volume for this code." This pattern points to an operational capability to process very large volumes of low-paid point-of-care or self-test COVID claims alongside its higher-revenue genetic assays.

    The breadth of genetic targets billed spans oncology (e.g., 81334 RUNX, 81311 NRAS, 81351 TP53), hematologic markers (e.g., 81279 JAK2, 81339 MPL), metabolic and inherited conditions (e.g., 81249 G6PD, 81250 G6PC, 81223 CFTR), and high-risk cancer predisposition testing (e.g., 81307 BRCA2/PALB2, 81162 BRCA1/BRCA2). This diversity of assay types supports the interpretation of a comprehensive genomics platform capable of both targeted variant testing and broader sequence-based services.

    Administrative and attribution limits constrain further competitive analysis: city, state, taxonomy, and NPI enumeration date are listed as unknown, which prevents confirming corporate affiliation, facility type, geographic service area, or tenure on file. Those unknowns limit the ability to assess market share, growth trajectory, or to reconcile Medicare activity with state-level provider lists or Medicaid enrollment records.