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NF1 (neurofibromin 1)
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Curator:
Instituto Nacional del Cancer
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Template
: Template(s) used to detect the sequence variant; DNA = genomic DNA, RNA = RNA (cDNA).
All options:
DNA
RNA = RNA (cDNA)
Protein
? = unknown
Technique
: Technique(s) used to identify the sequence variant.
All options:
? = Unknown
SEQ-NG = Next-Generation Sequencing
SEQ = SEQuencing
MLPA = Multiplex Ligation-dependent Probe Amplification
SEQ-NG-H = Next-Generation Sequencing - Helicos
SEQ-NG-I = Next-Generation Sequencing - Illumina/Solexa
SEQ-NG-R = Next-Generation Sequencing - Roche/454
SEQ-NG-S = Next-Generation Sequencing - SOLiD
arrayCGH = array for Comparative Genomic Hybridisation
arraySEQ = array for resequencing
arraySNP = array for SNP typing
arrayCNV = array for Copy Number Variation (SNP and CNV probes)
BESS = Base Excision Sequence Scanning
CMC = Chemical Mismatch Cleavage
CNV
CSCE = Conformation Sensitive Capillary Electrophoresis
DECoN = Detection of Exon Copy Number variants
DGGE = Denaturing-Gradient Gel-Electrophoresis
DHPLC = Denaturing High-Performance Liquid Chromatography
DOVAM = Detection Of Virtually All Mutations (SSCA variant)
ddF = dideoxy Fingerprinting
DSCA = Double-Strand DNA Conformation Analysis
EMC = Enzymatic Mismatch Cleavage
HD = HeteroDuplex analysis
MCA = high-resolution Melting Curve Analysis (hrMCA)
IHC = Immuno-Histo-Chemistry
MAPH = Multiplex Amplifiable Probe Hybridisation
Northern = Northern blotting
PCR = Polymerase Chain Reaction
PCRdig = PCR + restriction enzyme digestion
PCRlr = PCR, long-range
PCRm = PCR, multiplex
PCRq = PCR, quantitative
PAGE = Poly-Acrylamide Gel-Electrophoresis
PTT = Protein Truncation Test
PFGE = Pulsed-Field Gel-Electrophoresis (+Southern)
RT-PCR = Reverse Transcription and PCR
SBE = Single Base Extension
SSCA = Single-Strand DNA Conformation polymorphism Analysis (SSCP)
SSCAf = SSCA, fluorescent (SSCP)
Southern = Southern blotting
TaqMan = TaqMan assay
Western = Western Blotting
in-house algorithm for CNV
z-score-CNV = z-score based algorithm for CNV detection in targeted NGS
Lab
: Name of the Laboratory that performed the screening.
All options:
ARGENETICS
ARGENOMICS - Fundacion Investigar
Biocodices S.A.
Biogenotec
BIOMAKERS Molecular Pathology & Research
Bionet
Centro de Diagnostico Molecular (CDM)
Centro de Educación Médica e Investigaciones Clínicas (CEMIC)
Centro de Estudios Geneticos (CEG)
Centro de Investigaciones Endocrinologicas “Dr. Cesar Bergada” (CEDIE)
Centro Nacional de Genetica Medica "Dr. Eduardo E. Castilla" (CENAGEM)
Centro Privado Internacional de Medicina Personalizada - CEPIMP Genomics
CIBIC – Centro de Diagnóstico Médico de Alta Complejidad S.A. - HERITAS
CITOGEN.LAB
Clínica Universitaria Reina Fabiola
Dasa Genómica - Genia
Diagnus Lab
Domeq&Lafage
Fundacion BIOGEN
Fundación para el Progreso de la Medicina
FUNDAGEN S.A.
Gammalab - Grupo Gamma S.A.
GENDA
Genesia - Progenitest
Genologica laboratorio de análisis genéticos
GENOS
Grupo de investigacion en Genetica Aplicada (GIGA)
Hospital Alemán
Hospital de Alta Complejidad El Calafate - SAMIC
Hospital de Gastroenterología Dr. Carlos Bonorino Udaondo
Hospital Italiano de Buenos Aires
Hospital Privado Centro Médico de Córdoba
Hospital Universitario Austral
IACA Laboratorios
IBC Laboratorios
Instituto Alexander Fleming
Laboratorio Barros
Laboratorio de Biologia Celular y Molecular IHEM-CONICET CCT Mendoza
Laboratorio de Medicina Genomica - Facultad de Medicina - UNNE
Laboratorio Dr. Rapela
Laboratorio Dra. Marta Cortelezzi
Laboratorio Fares Taie
Laboratorio Flores
Laboratorio Hidalgo S.A.
Laboratorio High Medic Group S.A.
Laboratorio Integral SRL
Laboratorio Maipu
Laboratorio Motter
Laboratorio NANNI
Laboratorio PampaGEN
Laboratorio Tucumán
Laboratorios Turner
LACE Laboratorios
LEB (Laboratorio de Especialidades Bioquimicas)
MANLAB
MEDgenomica
PRICAI-Primer Centro Argentino de Inmunogenética-Fundación Favaloro
Sanatorio Allende
Stamboulian Laboratorio
STEM
VZ Laboratorios
Zoigen
AMBRY GENETICS
Baylor Genetics
Blueprint Genetics
CENTOGENE
COLOR
GENE ONE
Health in code
Iden Gene
IMEGEN
INVITAE
Laboratorio ATGen (E)
Laboratorio ATGen
MACROGEN
Myriad Genetics
SENTIS
Sistemas Genómicos
------
Color
Genda
Genda/Color
Genesia
Genesia/Invitae
Genia/Invitae
Genia/Color
Genia
Genos
Genos/Color
Hospital Privado Centro Médico de Córdoba
Hospital Privado Centro médico de Córdoba/IACA
Héritas
IACA
Invitae
AbaCid
Ambry Genetics
Alexander Fleming
Alexander Fleming/Baylor College
Alexander Fleming/Genesia-INVITAE
Argenomics
Baylor Genetics
BIOGEN
Biogenotec
BIOMAKERS Molecular Pathology & Research
BIONET
Blueprint Genetics
CEDIE
CEG
CEMIC
Centro de diagnóstico molecular
CEPIMP Genomics
CeNaGeM
Centogene
CIBIC
CIBIC/Héritas
Ciscato&Sharovsky
Clinica Universitaria Reina Fabiola
DIAGNUS LAB
Domeq&Lafage
Dr. Rapela
Fares Taie
FARESTAIE/Héritas
FAVALORO-PRICAI
Fundación para el Progreso de la Medicina
Fundación para el Progreso de la Medicina/CIBIC/Héritas
Fundagen
Gammalab
GeneDx
GIGA
Health in code
Hidalgo
High Medic Group
Hospital Alemán
Hospital de Gastroenterologia
Sanatorio Allende
MEDgenomica
LACE
HEMA
Centro médico de Córdoba
DASA-INVITAE
Bioscreen Rosario
x
Remarks
: Remarks
Date of test
: Date in which the results of the test were informed to the pacient
Type of test
: Type of test
All options:
Known familial mutation
Multigenetic panel
Specific pathology
Ashkenazi panel
Germline variant found in somatic testing
Whole exome
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Numeric
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all entries containing 'South Asian', but not containing 'South East Asian'
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19 entries on 1 page. Showing entries 1 - 19.
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How to query
Screening ID
Individual ID
Template
Technique
Lab
Remarks
Date of test
Type of test
Variants found
Owner
0000000109
00000100
DNA
SEQ-NG
Dasa Genómica - Genia;INVITAE
Invitae Breast Cancer Panel
20-apr-2017
Multigenetic panel
20
Lina Nuñez-Private Practice
0000000284
00000243
DNA
SEQ-NG
Dasa Genómica - Genia;INVITAE
Invitae Breast Cancer Panel
31-jul-2017
Multigenetic panel
1
Norma Rossi-Hospital de Córdoba
0000000681
00000594
DNA
SEQ-NG
IACA
CNVs screening for BRCA1, BRCA2, PALB2, RAD51D, RAD51C, TP53
4-may-2018
Multigenetic panel
1
Lina Nuñez-Private Practice
0000000753
00000651
DNA
SEQ-NG;z-score-CNV
Héritas
-
30-jul-2018
Multigenetic panel
1
Alvaro Yanzi-Instituto San Marcos
0000001068
00000897
DNA
z-score-CNV
Héritas
-
3-mar-2018
Multigenetic panel
-
Laura Vargas Roig-IMBECU
0000001079
00000901
DNA
z-score-CNV
Héritas
-
16-may-2018
Multigenetic panel
-
Laura Vargas Roig-IMBECU
0000001284
00001073
DNA
CNV;SEQ-NG
IACA
-
27-dec-2019
Multigenetic panel
20
Silvina Sisterna-Hospital de Comunidad
0000001393
00001166
DNA
CNV;SEQ-NG
Invitae (deriv. Genia)
-
24-oct-2019
Multigenetic panel
1
Pablo Kalfayan-Hospital Italiano
0000001407
00001177
DNA
CNV;SEQ-NG
Hospital Universitario Austral
Test realizado en Laboratorio de Derivación
28-jan-2020
Multigenetic panel
1
Pablo Kalfayan-Hospital Italiano
0000001524
00001285
DNA
CNV;SEQ-NG
IACA
CNV test of BRCA1, BRCA2, PALB2, RAD51C, RAD51D, TP53.
2-aug-2018
Multigenetic panel
32
Silvina Sisterna-Hospital de Comunidad
0000001553
00001314
DNA
CNV;SEQ-NG
Genda
test performed in a laboratory abroad, which is certified by CLIA and CAP
11-jul-2019
Multigenetic panel
-
Jesica Ramirez-Hospital Central de Mendoza
0000001559
00001320
DNA
CNV;SEQ-NG
Invitae (deriv. Genda)
Paraganglyoma-Pheochromocytoma Panel
23-oct-2019
Multigenetic panel
-
Jesica Ramirez-Hospital Central de Mendoza
0000001560
00001321
DNA
CNV;SEQ-NG
Genda
test performed in a laboratory abroad, which is certified by CLIA and CAP
4-jun-2019
Specific pathology
1
Jesica Ramirez-Hospital Central de Mendoza
0000002011
00001732
DNA
SEQ-NG
CIBIC/Héritas
Sindrome cáncer hereditario mama y ovarios (14 genes) ATM, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, NBN, NF1, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53
23-jan-2018
Multigenetic panel
1
Instituto Nacional del Cancer
0000002013
00001734
DNA
SEQ-NG
CIBIC/Héritas
Sindrome cáncer hereditario mama y ovarios (14 genes) ATM, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, NBN, NF1, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53
04-oct-2018
Multigenetic panel
1
Marcela Lopez-CEMAFE
0000002021
00001742
DNA
SEQ-NG
CIBIC/Héritas
Sindrome cáncer hereditario mama y ovarios (14 genes) ATM, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, NBN, NF1, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53
20-jul-2018
Multigenetic panel
1
Marcela Lopez-CEMAFE
0000002117
00001832
DNA
SEQ-NG
Genia/Invitae
Panel cancer mama (12 genes) ATM, BARD1, BRCA1, BRCA2, CDH1, CHEK2, NBN, NF1, PALB2, PTEN, STK11, TP53
01-sep-2021
Multigenetic panel
1
Pablo Kalfayan-Hospital Italiano
0000002353
00002066
DNA
SEQ-NG
Invitae
Invitae Breast Cancer Panel (13 genes) ATM*, BARD1, BRCA1, BRCA2, CDH1, CHEK2, NF1*, PALB2, PTEN*, RAD51C, RAD51D, STK11, TP53
26-may-2022
Multigenetic panel
Not yet submitted
Lina Nuñez-Private Practice
0000002457
00002166
DNA
SEQ-NG
Genesia - Progenitest;Instituto Alexander Fleming;INVITAE
-
01-06-2022
Multigenetic panel
-
Lina Nuñez-Private Practice
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