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6,967 Results - per page

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Name Proper Citation Organism Disease Comments Defining Citation Category Sex Synonyms Vendor Catalog Number Cross References Hierarchy Originate from Same Individual ID Record Last Update Mentions Count
BO0737
 
Resource Report
Resource Website
ECACC Cat# 93071404, RRID:CVCL_8T27 Homo sapiens (Human) Karyotypic information: 46,XY,-22,+der(22)(T) (ECACC=93071404)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93071404 ECACC:93071404,
Wikidata:Q54797776
CVCL_8T27 2026-07-25 05:26:58 0
BO0574
 
Resource Report
Resource Website
ECACC Cat# 93020207, RRID:CVCL_8T12 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93020207 ECACC:93020207,
Wikidata:Q54797752
CVCL_8T12 2026-07-25 05:26:58 0
BO0392
 
Resource Report
Resource Website
ECACC Cat# 92062610, RRID:CVCL_8T02 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92062610 ECACC:92062610,
Wikidata:Q54797736
CVCL_8T02 2026-07-25 05:27:01 0
BO0389
 
Resource Report
Resource Website
ECACC Cat# 92061815, RRID:CVCL_8T01 Homo sapiens (Human) Turner syndrome Karyotypic information: 46,X,del(X)(qter-cen) (ECACC=92061815)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92061815 ECACC:92061815,
Wikidata:Q54797734
CVCL_8T01 2026-07-25 05:26:57 0
BO0770
 
Resource Report
Resource Website
ECACC Cat# 93081915, RRID:CVCL_8T31 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 93081915 ECACC:93081915,
Wikidata:Q54797784
CVCL_8T31 2026-07-25 05:26:58 0
BO0790
 
Resource Report
Resource Website
ECACC Cat# 93101104, RRID:CVCL_8T34 Homo sapiens (Human) Developmental delay Karyotypic information: 47,XY,+marker (ECACC=93101104)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93101104 ECACC:93101104,
Wikidata:Q54797812
CVCL_8T34 2026-07-25 05:26:58 0
BO0401
 
Resource Report
Resource Website
ECACC Cat# 92070702, RRID:CVCL_8T04 Homo sapiens (Human) Fragile X syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92070702 ECACC:92070702,
Wikidata:Q54797738
CVCL_8T04 2026-07-25 05:26:57 0
BO0663
 
Resource Report
Resource Website
ECACC Cat# 93050613, RRID:CVCL_8T18 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93050613 ECACC:93050613,
Wikidata:Q54797761
CVCL_8T18 2026-07-25 05:26:58 0
BO0563
 
Resource Report
Resource Website
ECACC Cat# 93011408, RRID:CVCL_8T10 Homo sapiens (Human) Beckwith-Wiedemann syndrome Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93011408 ECACC:93011408,
Wikidata:Q54797749
CVCL_8T10 2026-07-25 05:26:58 0
BO0718
 
Resource Report
Resource Website
ECACC Cat# 93061804, RRID:CVCL_8T23 Homo sapiens (Human) Angelman syndrome Karyotypic information: 46,XY,del(15)(pter->q11.2::q13->qter) (ECACC=93061804)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93061804 ECACC:93061804,
Wikidata:Q54797769
CVCL_8T23 2026-07-25 05:27:02 0
BO0851
 
Resource Report
Resource Website
ECACC Cat# 93112512, RRID:CVCL_8T43 Homo sapiens (Human) Karyotypic information: 46,X,ringY; 46,X,marY; 47,X,ring,marY (ECACC=93112512)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93112512 ECACC:93112512,
Wikidata:Q54797825
CVCL_8T43 2026-07-25 05:26:59 0
BO0707
 
Resource Report
Resource Website
ECACC Cat# 93061108, RRID:CVCL_8T21 Homo sapiens (Human) Karyotypic information: 46,XX,12q+ (ECACC=93061108)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 93061108 ECACC:93061108,
Wikidata:Q54797766
CVCL_8T21 2026-07-25 05:26:58 0
BO0471
 
Resource Report
Resource Website
ECACC Cat# 92101202, RRID:CVCL_8T08 Homo sapiens (Human) Karyotypic information: 46,XX,t(4;6)(q31.3;p21.3) (ECACC=92101202)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92101202 ECACC:92101202,
Wikidata:Q54797744
CVCL_8T08 2026-07-25 05:27:01 0
BO0772
 
Resource Report
Resource Website
ECACC Cat# 93082627, RRID:CVCL_8T32 Homo sapiens (Human) 22q11.2 deletion syndrome Karyotypic information: 46,XY,del(22)(q11.2) (ECACC=93082627)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 93082627 ECACC:93082627,
Wikidata:Q54797785
CVCL_8T32 2026-07-25 05:27:02 0
BO0723
 
Resource Report
Resource Website
ECACC Cat# 93062506, RRID:CVCL_8T26 Homo sapiens (Human) Karyotypic information: 46,XX,5q+ (ECACC=93062506)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 93062506 ECACC:93062506,
Wikidata:Q54797774
CVCL_8T26 2026-07-25 05:27:02 0
BO0388
 
Resource Report
Resource Website
ECACC Cat# 92061814, RRID:CVCL_8T00 Homo sapiens (Human) Cat-eye syndrome Karyotypic information: 47,XX,+mar (ECACC=92061814)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92061814 ECACC:92061814,
Wikidata:Q54797732
CVCL_8T00 2026-07-25 05:26:57 0
BO0603
 
Resource Report
Resource Website
ECACC Cat# 93022607, RRID:CVCL_8T15 Homo sapiens (Human) Karyotypic information: 46,XX,t(4;10)(q27;q25) (ECACC=93022607)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 93022607 ECACC:93022607,
Wikidata:Q54797758
CVCL_8T15 2026-07-25 05:26:58 0
BO0436
 
Resource Report
Resource Website
ECACC Cat# 92080401, RRID:CVCL_8T06 Homo sapiens (Human) Karyotypic information: 46,XY,t(1;22)(p36;p12) (ECACC=92080401)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92080401 ECACC:92080401,
Wikidata:Q54797741
CVCL_8T06 2026-07-25 05:26:58 0
BO0719
 
Resource Report
Resource Website
ECACC Cat# 93061805, RRID:CVCL_8T24 Homo sapiens (Human) Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 93061805 ECACC:93061805,
Wikidata:Q54797771
CVCL_8T24 2026-07-25 05:26:58 0
BO0841
 
Resource Report
Resource Website
ECACC Cat# 93111705, RRID:CVCL_8T42 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 93111705 ECACC:93111705,
Wikidata:Q54797823
CVCL_8T42 2026-07-25 05:26:59 0

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