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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
DD1036
 
Resource Report
Resource Website
ECACC Cat# 92102919, RRID:CVCL_9D54 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92102919 ECACC:92102919,
Wikidata:Q54829487
CVCL_9D54 2026-08-15 04:26:31 0
DD1046
 
Resource Report
Resource Website
ECACC Cat# 92110204, RRID:CVCL_AQ63 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92110204 ECACC:92110204,
Wikidata:Q54829496
CVCL_AQ63 2026-08-15 04:26:31 0
DD1095
 
Resource Report
Resource Website
ECACC Cat# 92120703, RRID:CVCL_9D88 Homo sapiens (Human) Trisomy 13 Karyotypic information: 46,XX,+13 [6/30] (ECACC=92120703)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 92120703 ECACC:92120703,
Wikidata:Q54829528
CVCL_9D88 2026-08-15 04:26:32 0
DD1039
 
Resource Report
Resource Website
ECACC Cat# 92102922, RRID:CVCL_9D57 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92102922 ECACC:92102922,
Wikidata:Q54829490
CVCL_9D57 2026-08-15 04:26:31 0
DD1110
 
Resource Report
Resource Website
ECACC Cat# 92121603, RRID:CVCL_9E00 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92121603 ECACC:92121603,
Wikidata:Q54829540
CVCL_9E00 2026-08-15 04:26:32 0
DD1085
 
Resource Report
Resource Website
ECACC Cat# 92112742, RRID:CVCL_9D83 Homo sapiens (Human) Karyotypic information: 46,XX,-7,+der(7),inv ins(7:12)?(p21.2;q15q22)pat (ECACC=92112742)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 92112742 ECACC:92112742,
Wikidata:Q54829523
CVCL_9D83 2026-08-15 04:26:32 0
DD1055
 
Resource Report
Resource Website
ECACC Cat# 92111103, RRID:CVCL_9D67 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92111103 ECACC:92111103,
Wikidata:Q54829507
CVCL_9D67 2026-08-15 04:26:31 0
DD1109
 
Resource Report
Resource Website
ECACC Cat# 92121602, RRID:CVCL_9D99 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92121602 ECACC:92121602,
Wikidata:Q54829539
CVCL_9D99 2026-08-15 04:26:32 0
DD1075
 
Resource Report
Resource Website
ECACC Cat# 92112017, RRID:CVCL_9D78 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92112017 ECACC:92112017,
Wikidata:Q54829518
CVCL_9D78 2026-08-15 04:26:32 0
DD1051
 
Resource Report
Resource Website
ECACC Cat# 92111001, RRID:CVCL_9D64 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92111001 ECACC:92111001,
Wikidata:Q54829500
CVCL_9D64 2026-08-15 04:26:31 0
DD1089
 
Resource Report
Resource Website
ECACC Cat# 92120401, RRID:CVCL_9D84 Homo sapiens (Human) Karyotypic information: 46,XY,del(1)(pter->q43) (ECACC=92120401)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92120401 ECACC:92120401,
Wikidata:Q54829524
CVCL_9D84 2026-08-15 04:26:31 0
DD1048
 
Resource Report
Resource Website
ECACC Cat# 92110410, RRID:CVCL_9D62 Homo sapiens (Human) Trisomy 15 Karyotypic information: 47,XX,+15 (ECACC=92110410)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 92110410 ECACC:92110410,
Wikidata:Q54829498
CVCL_9D62 2026-08-15 04:26:31 0
DD1108
 
Resource Report
Resource Website
ECACC Cat# 92121601, RRID:CVCL_9D98 Homo sapiens (Human) Turner syndrome Karyotypic information: 45,X0 (ECACC=92121601)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 92121601 ECACC:92121601,
Wikidata:Q54829538
CVCL_9D98 2026-08-15 04:26:32 0
DD1103
 
Resource Report
Resource Website
ECACC Cat# 92121014, RRID:CVCL_9D94 Homo sapiens (Human) Karyotypic information: 46,XX,-7,+der(7),inv ins(7:12)?(p21.2;q15q22)pat (ECACC=92121014)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 92121014 ECACC:92121014,
Wikidata:Q54829534
CVCL_9D94 2026-08-15 04:26:32 0
DD1106
 
Resource Report
Resource Website
ECACC Cat# 92121505, RRID:CVCL_9D97 Homo sapiens (Human) Karyotypic information: 47,XX,+pseudic(15)(pter->q13::q13->pter); de novo (ECACC=92121505)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92121505 ECACC:92121505,
Wikidata:Q54829537
CVCL_9D97 2026-08-15 04:26:32 0
DD1035
 
Resource Report
Resource Website
ECACC Cat# 92102918, RRID:CVCL_9D53 Homo sapiens (Human) Karyotypic information: 46,XY,t(3;10)(p23;q21.2) (ECACC=92102918)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92102918 ECACC:92102918,
Wikidata:Q54829486
CVCL_9D53 2026-08-15 04:26:30 0
DD1099
 
Resource Report
Resource Website
ECACC Cat# 92120804, RRID:CVCL_9D91 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92120804 ECACC:92120804,
Wikidata:Q54829531
CVCL_9D91 2026-08-15 04:26:32 0
DD1097
 
Resource Report
Resource Website
ECACC Cat# 92120802, RRID:CVCL_9D89 Homo sapiens (Human) Karyotypic information: 46,XX,17p+ (ECACC=92120802)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92120802 ECACC:92120802,
Wikidata:Q54829529
CVCL_9D89 2026-08-15 04:26:32 0
DD1049
 
Resource Report
Resource Website
ECACC Cat# 92110609, RRID:CVCL_9D63 Homo sapiens (Human) Karyotypic information: 46,XY; 47,XY,+mar(15); de novo (ECACC=92110609)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 92110609 ECACC:92110609,
Wikidata:Q54829499
CVCL_9D63 2026-08-15 04:26:31 0
DD1090
 
Resource Report
Resource Website
ECACC Cat# 92120905, RRID:CVCL_9D85 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92120905 ECACC:92120905,
Wikidata:Q54829525
CVCL_9D85 2026-08-15 04:26:32 0

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