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256,031 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
DD0666
 
Resource Report
Resource Website
RRID:CVCL_9B30 Homo sapiens (Human) Karyotypic information: 46,XY,t(1;13)(p22;q32)pat (ECACC=92030643)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:92030643,
Wikidata:Q54829178
CVCL_9B30 2026-08-15 04:26:25 0
DD0713
 
Resource Report
Resource Website
RRID:CVCL_9B57 Homo sapiens (Human) Karyotypic information: 46,XX; 47,XX,+9 (ECACC=92042301)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:92042301,
Wikidata:Q54829213
CVCL_9B57 2026-08-15 04:26:26 0
DD0677
 
Resource Report
Resource Website
RRID:CVCL_9B38 Homo sapiens (Human) Trisomy 18 Karyotypic information: 47,XY,+18 (ECACC=92031805)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:92031805,
Wikidata:Q54829194
CVCL_9B38 2026-08-15 04:26:23 0
DD0666
 
Resource Report
Resource Website
ECACC Cat# 92030643, RRID:CVCL_9B30 Homo sapiens (Human) Karyotypic information: 46,XY,t(1;13)(p22;q32)pat (ECACC=92030643)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92030643 ECACC:92030643,
Wikidata:Q54829178
CVCL_9B30 2026-08-15 04:26:22 0
DD0674
 
Resource Report
Resource Website
ECACC Cat# 92031104, RRID:CVCL_9B35 Homo sapiens (Human) Karyotypic information: 46,XX,t(4;9)(q21;q13); de novo (ECACC=92031104)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92031104 ECACC:92031104,
Wikidata:Q54829191
CVCL_9B35 2026-08-15 04:26:23 0
DD0682
 
Resource Report
Resource Website
ECACC Cat# 92031913, RRID:CVCL_9B40 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92031913 ECACC:92031913,
Wikidata:Q54829196
CVCL_9B40 2026-08-15 04:26:25 0
DD0675
 
Resource Report
Resource Website
ECACC Cat# 92031314, RRID:CVCL_9B36 Homo sapiens (Human) Karyotypic information: 46,XX,-7,+der(7),t(7;11)(q36.1;q23.3)mat (ECACC=92031314)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 92031314 ECACC:92031314,
Wikidata:Q54829192
CVCL_9B36 2026-08-15 04:26:23 0
DD0701
 
Resource Report
Resource Website
RRID:CVCL_9B49 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC:92041022,
Wikidata:Q54829205
CVCL_9B49 2026-08-15 04:26:23 0
DD0683
 
Resource Report
Resource Website
ECACC Cat# 92032707, RRID:CVCL_9B41 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92032707 ECACC:92032707,
Wikidata:Q54829197
CVCL_9B41 2026-08-15 04:26:23 0
DD0661
 
Resource Report
Resource Website
ECACC Cat# 92030622, RRID:CVCL_9B27 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92030622 ECACC:92030622,
Wikidata:Q54829175
CVCL_9B27 2026-08-15 04:26:22 0
DD0706
 
Resource Report
Resource Website
RRID:CVCL_9B52 Homo sapiens (Human) Congenital hydrocephalus Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:92041520,
Wikidata:Q54829208
CVCL_9B52 2026-08-15 04:26:23 0
DD0711
 
Resource Report
Resource Website
RRID:CVCL_9B56 Homo sapiens (Human) Congenital hydrocephalus Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:92042109,
Wikidata:Q54829212
CVCL_9B56 2026-08-15 04:26:23 0
DD0654
 
Resource Report
Resource Website
ECACC Cat# 92030202, RRID:CVCL_9B24 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92030202 ECACC:92030202,
Wikidata:Q54829172
CVCL_9B24 2026-08-15 04:26:22 0
DD0682
 
Resource Report
Resource Website
RRID:CVCL_9B40 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:92031913,
Wikidata:Q54829196
CVCL_9B40 2026-08-15 04:26:23 0
DD0631
 
Resource Report
Resource Website
ECACC Cat# 92021921, RRID:CVCL_9B08 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92021921 ECACC:92021921,
Wikidata:Q54829155
CVCL_9B08 2026-08-15 04:26:22 0
DD0655
 
Resource Report
Resource Website
RRID:CVCL_9B25 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:92030301,
Wikidata:Q54829173
CVCL_9B25 2026-08-15 04:26:22 0
DD0689
 
Resource Report
Resource Website
RRID:CVCL_9B44 Homo sapiens (Human) Congenital hydrocephalus Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC:92033007,
Wikidata:Q54829200
CVCL_9B44 2026-08-15 04:26:23 0
DD0665
 
Resource Report
Resource Website
RRID:CVCL_9B29 Homo sapiens (Human) Karyotypic information: 46,XY,t(1;13)(p22;q32)(?O) (ECACC=92030642)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:92030642,
Wikidata:Q54829177
CVCL_9B29 2026-08-15 04:26:22 0
DD0700
 
Resource Report
Resource Website
ECACC Cat# 92041021, RRID:CVCL_9B48 Homo sapiens (Human) Trisomy 21 Karyotypic information: 47,XY,+21 (ECACC=92041021)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 92041021 ECACC:92041021,
Wikidata:Q54829204
CVCL_9B48 2026-08-15 04:26:23 0
DD0705
 
Resource Report
Resource Website
RRID:CVCL_9B51 Homo sapiens (Human) Karyotypic information: 46,XY,del(20)(p11.21;p11.23); de novo (ECACC=92041418)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC:92041418,
Wikidata:Q54829207
CVCL_9B51 2026-08-15 04:26:25 0

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