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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
DD3450
 
Resource Report
Resource Website
ECACC Cat# 99080629, RRID:CVCL_9N08 Homo sapiens (Human) Population: Caucasian., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 99080629 ECACC:99080629,
Wikidata:Q54830749
CVCL_9N08 2026-07-25 04:30:14 0
DD3439
 
Resource Report
Resource Website
ECACC Cat# 99070736, RRID:CVCL_9N05 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 99070736 ECACC:99070736,
Wikidata:Q54830744
CVCL_9N05 2026-07-25 04:30:14 0
DD3479
 
Resource Report
Resource Website
ECACC Cat# 99112430, RRID:CVCL_9P75 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 99112430 ECACC:99112430,
Wikidata:Q54830760
CVCL_9P75 2026-07-25 04:30:15 0
DD3480
 
Resource Report
Resource Website
ECACC Cat# 99120301, RRID:CVCL_9P76 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 99120301 ECACC:99120301,
Wikidata:Q54830761
CVCL_9P76 2026-07-25 04:30:15 0
DD3535
 
Resource Report
Resource Website
ECACC Cat# 00042514, RRID:CVCL_9P93 Homo sapiens (Human) Karyotypic information: 46,Y,inv(X)(q13.1;q24) (ECACC=00042514)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 00042514 ECACC:00042514,
Wikidata:Q54830791
CVCL_9P93 2026-07-25 04:30:16 0
DD3482
 
Resource Report
Resource Website
ECACC Cat# 99120701, RRID:CVCL_9N13 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 99120701 ECACC:99120701,
Wikidata:Q54830763
CVCL_9N13 2026-07-25 04:30:15 0
DD3499
 
Resource Report
Resource Website
ECACC Cat# 00013124, RRID:CVCL_9P79 Homo sapiens (Human) Karyotypic information: 47,XX,+mar (ECACC=00013124)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 00013124 ECACC:00013124,
Wikidata:Q54830767
CVCL_9P79 2026-07-25 04:30:15 0
DD3559
 
Resource Report
Resource Website
ECACC Cat# 00062916, RRID:CVCL_9P99 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 00062916 ECACC:00062916,
Wikidata:Q54830806
CVCL_9P99 2026-07-25 04:30:16 0
DD3533
 
Resource Report
Resource Website
ECACC Cat# 00041319, RRID:CVCL_9N20 Homo sapiens (Human) Lissencephaly Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 00041319 ECACC:00041319,
Wikidata:Q54830790
CVCL_9N20 2026-07-25 04:30:16 0
DD3510
 
Resource Report
Resource Website
ECACC Cat# 00022416, RRID:CVCL_9P86 Homo sapiens (Human) Karyotypic information: 46,XX,inv(9)(q22.33;q34.3)mat (ECACC=00022416)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 00022416 ECACC:00022416,
Wikidata:Q54830774
CVCL_9P86 2026-07-25 04:30:15 0
DD3481
 
Resource Report
Resource Website
ECACC Cat# 99120302, RRID:CVCL_9N12 Homo sapiens (Human) Turner syndrome Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 99120302 ECACC:99120302,
Wikidata:Q54830762
CVCL_9N12 2026-07-25 04:30:15 0
DD3553
 
Resource Report
Resource Website
ECACC Cat# 00061421, RRID:CVCL_9P97 Homo sapiens (Human) Karyotypic information: 46,XY,del(1)(p36.2) (ECACC=00061421)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Male ECACC 00061421 ECACC:00061421,
Wikidata:Q54830803
CVCL_9P97 2026-07-25 04:30:16 0
DD3546
 
Resource Report
Resource Website
ECACC Cat# 00051011, RRID:CVCL_9P94 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 00051011 ECACC:00051011,
Wikidata:Q54830799
CVCL_9P94 2026-07-25 04:30:16 0
DD3467
 
Resource Report
Resource Website
ECACC Cat# 99100611, RRID:CVCL_9P73 Homo sapiens (Human) Karyotypic information: 46,XX,inv(13)(q33.2;q34)pat (ECACC=99100611)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 99100611 ECACC:99100611,
Wikidata:Q54830756
CVCL_9P73 2026-07-25 04:30:15 0
DD3509
 
Resource Report
Resource Website
ECACC Cat# 00021807, RRID:CVCL_9P85 Homo sapiens (Human) Karyotypic information: 46,XY,inv(2)(p24.2;q35)pat (ECACC=00021807)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 00021807 ECACC:00021807,
Wikidata:Q54830773
CVCL_9P85 2026-07-25 04:30:15 0
DD3555
 
Resource Report
Resource Website
ECACC Cat# 00062022, RRID:CVCL_9N29 Homo sapiens (Human) Karyotypic information: 45,XY,der(14;21)(q10;q10)mat (ECACC=00062022)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 00062022 ECACC:00062022,
Wikidata:Q54830804
CVCL_9N29 2026-07-25 04:30:16 0
DD3540
 
Resource Report
Resource Website
ECACC Cat# 00050204, RRID:CVCL_9N22 Homo sapiens (Human) Karyotypic information: 46,XX,t(11;22)(q25;?q13.1) (ECACC=00050204)., Part of: ECACC chromosomal abnormality collection. Finite cell line Female ECACC 00050204 ECACC:00050204,
Wikidata:Q54830793
CVCL_9N22 2026-07-25 04:30:16 0
DD3518
 
Resource Report
Resource Website
ECACC Cat# 00031007, RRID:CVCL_9P88 Homo sapiens (Human) Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 00031007 ECACC:00031007,
Wikidata:Q54830783
CVCL_9P88 2026-07-25 04:30:15 0
DD3543
 
Resource Report
Resource Website
ECACC Cat# 00050604, RRID:CVCL_9N25 Homo sapiens (Human) Karyotypic information: 46,XX,ins(3;2)(p23;q13q23); de novo (ECACC=00050604)., Part of: ECACC chromosomal abnormality collection. Transformed cell line Female ECACC 00050604 ECACC:00050604,
Wikidata:Q54830796
CVCL_9N25 2026-07-25 04:30:16 0
DD3477
 
Resource Report
Resource Website
ECACC Cat# 99112428, RRID:CVCL_9N11 Homo sapiens (Human) Karyotypic information: 46,XY,t(5;13)(p11;p12) (ECACC=99112428)., Part of: ECACC chromosomal abnormality collection. Finite cell line Male ECACC 99112428 ECACC:99112428,
Wikidata:Q54830759
CVCL_9N11 2026-07-25 04:30:15 0

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