GRCh37/hg19 4p14(chr4:38459610-38724190)x3 AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Apr 1, 2021
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV001836511.1

Allele description [Variation Report for GRCh37/hg19 4p14(chr4:38459610-38724190)x3]

GRCh37/hg19 4p14(chr4:38459610-38724190)x3

Gene:

KLF3:Kruppel like factor 3 [Gene - OMIM - HGNC]

Variant type:

copy number gain

Cytogenetic location:

4p14

Genomic location:

Chr4: 38459610 - 38724190 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 4p14(chr4:38459610-38724190)x3

HGVS:

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: CN517202

Recent activity

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MULTISPECIES: hypothetical protein [Haloferax]
MULTISPECIES: hypothetical protein [Haloferax]
gi|491119560|ref|WP_004978002.1|

Protein
MULTISPECIES: 30S ribosomal protein S17e [Haloferax]
MULTISPECIES: 30S ribosomal protein S17e [Haloferax]
gi|490142074|ref|WP_004042417.1|

Protein
GSTA3 glutathione S-transferase alpha 3 [Homo sapiens]
GSTA3 glutathione S-transferase alpha 3 [Homo sapiens]
Gene ID:2940

Gene
PREDICTED: Homo sapiens ring finger protein 24 (RNF24), transcript variant X1, m...
PREDICTED: Homo sapiens ring finger protein 24 (RNF24), transcript variant X1, mRNA
gi|2217334313|ref|XM_017027621.2|

Nucleotide
Leucoagaricus cupresseus isolate CA FUNDIS voucher FDS-CA-01621 small subunit ri...
Leucoagaricus cupresseus isolate CA FUNDIS voucher FDS-CA-01621 small subunit ribosomal RNA gene, partial sequence; internal transcribed spacer 1, 5.8S ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and large subunit ribosomal RNA gene, partial sequence
gi|2784013327|gb|PQ148090.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002096208	Quest Diagnostics Nichols Institute San Juan Capistrano	no assertion criteria provided	Uncertain significance (Apr 1, 2021)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002096208

Quest Diagnostics Nichols Institute San Juan Capistrano

no assertion criteria provided

Uncertain significance
(Apr 1, 2021)

germline

clinical testing

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Quest Diagnostics Nichols Institute San Juan Capistrano, SCV002096208.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Apr 23, 2022

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