DNA test

Dante Non Invasive Prenatal Test

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Our non-invasive testing method uses a small blood sample to make an accurate diagnosis of chromosomal conditions in your baby’s DNA.
The test involves 4 different kinds of comprehensive analyses that tests for genetic variations in your baby’s DNA.
Test for conditions such as Down Syndrome, Edward Syndrome and Turner Syndrome.
Understand your baby’s potential health conditions and plan in advance for any required care.
Access a comprehensive report that breaks down your baby’s chromosomal data.
Free worldwide shipping.

DNA exploration

In only a few weeks, you will receive your digital and comprehensive reports that breaks down your baby’s chromosomal data.

Understand your baby’s potential health conditions and plan in advance for any required care.

Fast and safe delivery, just purchase the kit and activate it using the Kit ID before testing.

Order your kit
Fast and safe delivery. Just purchase the kit and activate it using the Kit ID before testing.
Painless sampling
Contains an innovative blood collection kit. The sample must be carried out by a nurse, which you can request at your local medical practice.
Fast activation
Book the collection of your blood sample in a facility enabled for the service. You can find a list of providers here.
Digital results
You’ll receive your results in a few weeks, available as a report within our digital portal. The results are easy to read and share with your doctor.

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Aneuploidy Analysis
An aneuploidy analysis tests for an imbalance of chromosomes. This may refer to one or more missing or extra chromosomes, beyond the typical amount of 23.
Using this information, we can determine the following conditions:
Down syndrome
Occurs when an individual has 23 chromosomes
Edward syndrome
Occurs when an individual has 18 chromosomes
Patau syndrome
Occurs when an individual 13 chromosomes
Chromosome 1/22 Analysis
A Chromosome Analysis checks in detail the number and structure of all 23 pairs of chromosomes present in the baby’s DNA.
Analysis of Duplications / Deletions
It carries out the study of small chromosomal alterations from structural rearrangements (microduplications or microdeletions).
Deletions / duplications> 7Mb
Sensitivity: 74.1%
Specificity: 99,8%
X / Y Chromosome and fetal sex determination
It analyzes the child's gender and X / Y sex chromosome abnormalities (X trisomy, Jacobs, Klinefelter and Turner syndrome).
X / Y chromosome (XXX, XYY, XXY or X0)
Fetal Sex Classification Agreement> 99%
Sensitivity: 95.5%
Specificity: 93.3%