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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
DD2038
 
Resource Report
Resource Website
ECACC Cat# 94080817, RRID:CVCL_9I49 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 94080817 ECACC:94080817,
Wikidata:Q54830079
CVCL_9I49 2026-08-29 04:25:07 0
DD2042
 
Resource Report
Resource Website
ECACC Cat# 94081227, RRID:CVCL_9I52 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 94081227 ECACC:94081227,
Wikidata:Q54830082
CVCL_9I52 2026-08-29 04:25:07 0
DD2036
 
Resource Report
Resource Website
ECACC Cat# 94080815, RRID:CVCL_9I47 Homo sapiens (Human) Karyotypic information: 46,XY,dir dup(1)(q32.1;q42.1); de novo (ECACC=94080815)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 94080815 ECACC:94080815,
Wikidata:Q54830077
CVCL_9I47 2026-08-29 04:25:07 0
DD2077
 
Resource Report
Resource Website
ECACC Cat# 94090205, RRID:CVCL_9I67 Homo sapiens (Human) Karyotypic information: 46,XX,-7,+der(7),t(7;11)(q36.1;q23.3)pat (ECACC=94090205)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 94090205 ECACC:94090205,
Wikidata:Q54830100
CVCL_9I67 2026-08-29 04:25:07 0
DD2041
 
Resource Report
Resource Website
ECACC Cat# 94081226, RRID:CVCL_9I51 Homo sapiens (Human) Karyotypic information: 46,XY; 47,XY,+mar(13/21); de novo (ECACC=94081226)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 94081226 ECACC:94081226,
Wikidata:Q54830081
CVCL_9I51 2026-08-29 04:25:07 0
DD1993
 
Resource Report
Resource Website
ECACC Cat# 94071514, RRID:CVCL_9I31 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 94071514 ECACC:94071514,
Wikidata:Q54830059
CVCL_9I31 2026-08-29 04:25:06 0
DD2032
 
Resource Report
Resource Website
ECACC Cat# 94080811, RRID:CVCL_9I45 Homo sapiens (Human) Karyotypic information: 46,XX,-5,+der(5),t(5;11)(p15;p15)pat (ECACC=94080811)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 94080811 ECACC:94080811,
Wikidata:Q54830075
CVCL_9I45 2026-08-29 04:25:06 0
DD2029
 
Resource Report
Resource Website
ECACC Cat# 94080523, RRID:CVCL_9I43 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 94080523 ECACC:94080523,
Wikidata:Q54830073
CVCL_9I43 2026-08-29 04:25:07 0
DD2068
 
Resource Report
Resource Website
ECACC Cat# 94083002, RRID:CVCL_9I62 Homo sapiens (Human) Trisomy 18 Karyotypic information: 47,XX,+18 (ECACC=94083002)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 94083002 ECACC:94083002,
Wikidata:Q54830095
CVCL_9I62 2026-08-29 04:25:07 0
DD2073
 
Resource Report
Resource Website
ECACC Cat# 94083106, RRID:CVCL_9I65 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 94083106 ECACC:94083106,
Wikidata:Q54830098
CVCL_9I65 2026-08-29 04:25:07 0
DD2090
 
Resource Report
Resource Website
ECACC Cat# 94090717, RRID:CVCL_9I71 Homo sapiens (Human) Karyotypic information: 46,XX,t(1;3)(q21;q25)pat (ECACC=94090717)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 94090717 ECACC:94090717,
Wikidata:Q54830104
CVCL_9I71 2026-08-29 04:25:07 0
DD2044
 
Resource Report
Resource Website
ECACC Cat# 94081610, RRID:CVCL_9I54 Homo sapiens (Human) Charcot-Marie-Tooth disease Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 94081610 ECACC:94081610,
Wikidata:Q54830084
CVCL_9I54 2026-08-29 04:25:07 0
DD2058
 
Resource Report
Resource Website
ECACC Cat# 94082535, RRID:CVCL_9I60 Homo sapiens (Human) Karyotypic information: 46,XX,t(1;19)(q42.13;p13) (ECACC=94082535)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 94082535 ECACC:94082535,
Wikidata:Q54830090
CVCL_9I60 2026-08-29 04:25:07 0
DD1991
 
Resource Report
Resource Website
ECACC Cat# 94071512, RRID:CVCL_9I30 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 94071512 ECACC:94071512,
Wikidata:Q54830058
CVCL_9I30 2026-08-29 04:25:06 0
DD2056
 
Resource Report
Resource Website
ECACC Cat# 94082533, RRID:CVCL_9I58 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 94082533 ECACC:94082533,
Wikidata:Q54830088
CVCL_9I58 2026-08-29 04:25:07 0
DD2043
 
Resource Report
Resource Website
ECACC Cat# 94081228, RRID:CVCL_9I53 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 94081228 ECACC:94081228,
Wikidata:Q54830083
CVCL_9I53 2026-08-29 04:25:07 0
DD2054
 
Resource Report
Resource Website
ECACC Cat# 94082419, RRID:CVCL_9I57 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 94082419 ECACC:94082419,
Wikidata:Q54830087
CVCL_9I57 2026-08-29 04:25:07 0
DD2072
 
Resource Report
Resource Website
ECACC Cat# 94083104, RRID:CVCL_9I64 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 94083104 ECACC:94083104,
Wikidata:Q54830097
CVCL_9I64 2026-08-29 04:25:07 0
DD2048
 
Resource Report
Resource Website
ECACC Cat# 94081828, RRID:CVCL_9I56 Homo sapiens (Human) Trisomy 18 Karyotypic information: 47,XY,+18 (ECACC=94081828)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 94081828 ECACC:94081828,
Wikidata:Q54830086
CVCL_9I56 2026-08-29 04:25:07 0
DD2000
 
Resource Report
Resource Website
ECACC Cat# 94072230, RRID:CVCL_9Q32 Homo sapiens (Human) Turner syndrome Karyotypic information: 45,X0 (ECACC=94072230)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 94072230 ECACC:94072230,
Wikidata:Q54830063
CVCL_9Q32 2026-08-29 04:25:06 0

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