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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
DD2112
 
Resource Report
Resource Website
ECACC Cat# 94102709, RRID:CVCL_9I86 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 94102709 ECACC:94102709,
Wikidata:Q54830119
CVCL_9I86 2026-07-25 04:29:55 0
DD2100
 
Resource Report
Resource Website
ECACC Cat# 94092904, RRID:CVCL_9I78 Homo sapiens (Human) Charcot-Marie-Tooth disease Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 94092904 ECACC:94092904,
Wikidata:Q54830111
CVCL_9I78 2026-07-25 04:29:55 0
DD2169
 
Resource Report
Resource Website
ECACC Cat# 94122302, RRID:CVCL_9J15 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 94122302 ECACC:94122302,
Wikidata:Q54830151
CVCL_9J15 2026-07-25 04:29:56 0
DD2114
 
Resource Report
Resource Website
ECACC Cat# 941031166, RRID:CVCL_9I88 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 941031166 ECACC:941031166,
Wikidata:Q54830121
CVCL_9I88 2026-07-25 04:29:55 0
DD2132
 
Resource Report
Resource Website
ECACC Cat# 94111804, RRID:CVCL_9I96 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 94111804 ECACC:94111804,
Wikidata:Q54830129
CVCL_9I96 2026-07-25 04:29:56 0
DD2145
 
Resource Report
Resource Website
ECACC Cat# 94120409, RRID:CVCL_9J04 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 94120409 ECACC:94120409,
Wikidata:Q54830140
CVCL_9J04 2026-07-25 04:29:56 0
DD2184
 
Resource Report
Resource Website
ECACC Cat# 95011909, RRID:CVCL_9J20 Homo sapiens (Human) Karyotypic information: 46,XY,inv(10)(p11;q21.2) (ECACC=95011909)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 95011909 ECACC:95011909,
Wikidata:Q54830160
CVCL_9J20 2026-07-25 04:29:56 0
DD2125
 
Resource Report
Resource Website
ECACC Cat# 94111031, RRID:CVCL_9I93 Homo sapiens (Human) Karyotypic information: 46,XY,t(5;19)(p5:q19;q5:p19)pat (ECACC=94111031)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 94111031 ECACC:94111031,
Wikidata:Q54830126
CVCL_9I93 2026-07-25 04:29:55 0
DD2173
 
Resource Report
Resource Website
ECACC Cat# 95010707, RRID:CVCL_9J16 Homo sapiens (Human) Karyotypic information: 46,XX,t(1;12)(p22.1;q22)mat (ECACC=95010707)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 95010707 ECACC:95010707,
Wikidata:Q54830152
CVCL_9J16 2026-07-25 04:29:56 0
DD2108
 
Resource Report
Resource Website
ECACC Cat# 94102502, RRID:CVCL_9I82 Homo sapiens (Human) Holoprosencephaly Karyotypic information: 47,XX,+18 (ECACC=94102502)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 94102502 ECACC:94102502,
Wikidata:Q54830115
CVCL_9I82 2026-07-25 04:29:55 0
DD2314
 
Resource Report
Resource Website
ECACC Cat# 95061502, RRID:CVCL_9J60 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 95061502 ECACC:95061502,
Wikidata:Q54830210
CVCL_9J60 2026-07-25 04:29:58 0
DD2315
 
Resource Report
Resource Website
ECACC Cat# 95061503, RRID:CVCL_9J61 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 95061503 ECACC:95061503,
Wikidata:Q54830211
CVCL_9J61 2026-07-25 04:29:58 0
DD2276
 
Resource Report
Resource Website
ECACC Cat# 95052401, RRID:CVCL_9J43 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 95052401 ECACC:95052401,
Wikidata:Q54830192
CVCL_9J43 2026-07-25 04:29:57 0
DD2281
 
Resource Report
Resource Website
ECACC Cat# 95053002, RRID:CVCL_9J45 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 95053002 ECACC:95053002,
Wikidata:Q54830194
CVCL_9J45 2026-07-25 04:29:57 0
DD2305
 
Resource Report
Resource Website
ECACC Cat# 95060912, RRID:CVCL_AQ96 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Sex ambiguous ECACC 95060912 ECACC:95060912,
Wikidata:Q54830202
CVCL_AQ96 2026-07-25 04:29:58 0
DD2233
 
Resource Report
Resource Website
ECACC Cat# 95032230, RRID:CVCL_9J33 Homo sapiens (Human) Karyotypic information: 46,XX,t(7;11)(p12.2;p14.2) (ECACC=95032230)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 95032230 ECACC:95032230,
Wikidata:Q54830175
CVCL_9J33 2026-07-25 04:29:57 0
DD2313
 
Resource Report
Resource Website
ECACC Cat# 95061501, RRID:CVCL_9J59 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 95061501 ECACC:95061501,
Wikidata:Q54830209
CVCL_9J59 2026-07-25 04:29:58 0
DD2311
 
Resource Report
Resource Website
ECACC Cat# 95061208, RRID:CVCL_9J57 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 95061208 ECACC:95061208,
Wikidata:Q54830207
CVCL_9J57 2026-07-25 04:29:58 0
DD2261
 
Resource Report
Resource Website
ECACC Cat# 95050105, RRID:CVCL_9J41 Homo sapiens (Human) Trisomy 18 Karyotypic information: 47,XX,+18 (ECACC=95050105)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 95050105 ECACC:95050105,
Wikidata:Q54830188
CVCL_9J41 2026-07-25 04:29:57 0
DD2291
 
Resource Report
Resource Website
ECACC Cat# 95060215, RRID:CVCL_9J49 Homo sapiens (Human) Smith-Magenis syndrome Karyotypic information: 46,XY,del(17)(p11.2;p11.2) (ECACC=95060215)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 95060215 ECACC:95060215,
Wikidata:Q54830198
CVCL_9J49 2026-07-25 04:29:58 0

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