ScanLinc NIPT Options & Prices

NIPT SCREENINGPRICE
Prenatest
For the screening of aneuploidies in Chromosome 21 only – able to determine fetal sex.
£250
Ninalia 5
For the screening of aneuploidies in Chromosomes – 13,18,21, X and Y – able to determine fetal sex. The most common chromosomal aneuploidies detected are:-
Trisomy 21 – Downs Syndrome
Trisomy 18 – Edwards Syndrome
Trisomy 13 – Patau Syndrome
Monsomy X – Turner Syndrome
XXX – Trisomy X
XXY – Klinefelter Syndrome
XYY – Jacobs Syndrome.
£375 (£399 including scan)
Genesafe Inherited
This test screens for the five most common inherited recessive genetic disorders such as Cystic Fibrosis, Beta Thalassemia, Sickle cell Anaemia and Deafness Autosomal recessive type 1a and 1b.
£800
Genesafe De Novo
This test screens for 44 severe genetic disorders as a result of de novo mutations (a gene mutation that is not inherited) in 25 genes.
£800
PreNatalSafe Karyo
Analyses every chromosome in the genome providing karyotype-level insight. Tests for the most common aneuploidies as in Ninalia 5 but includes the less frequent chromosomal aneuploidies in Trisomy 1-22.
£800 – including scan
PreNatalSafe KaryoPlus
The most comprehensive NIPT in the world which analyses every chromosome in the genome as well as 9 clinically significant microdeletion syndromes which are:-
DiGeorge Syndrome
Wolf-Hirschhom Syndrome
Cri-du-chat Syndrome
Jacobsen Syndrome
Prader-Willi Syndrome
Langer-Gledion Syndrome
Angelman Syndrome
Smith-Magenis Syndrome
1p36 deletion Syndrome.
£1000 – including scan
Genesafe Complete
This test screens for both the inherited and de novo single-gene disorders with the combined test providing a complete picture of any potential risk to the pregnancy.
£1,050
PreNatalSafe Complete
is a combination of the two most powerful tests available worldwide PrenatalSafe KaryoPlus + GeneSafe complete are offered together at a reduced price.
£1500