GRCh37/hg19 9q32(chr9:116642144-117613527)x1 AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Dec 10, 2018
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:: RCV001006255.1

Allele description [Variation Report for GRCh37/hg19 9q32(chr9:116642144-117613527)x1]

GRCh37/hg19 9q32(chr9:116642144-117613527)x1

Genes:

AKNA:AT-hook transcription factor [Gene - OMIM - HGNC]
ATP6V1G1:ATPase H+ transporting V1 subunit G1 [Gene - OMIM - HGNC]
TNFSF15:TNF superfamily member 15 [Gene - OMIM - HGNC]
AMBP:alpha-1-microglobulin/bikunin precursor [Gene - OMIM - HGNC]
COL27A1:collagen type XXVII alpha 1 chain [Gene - OMIM - HGNC]
KIF12:kinesin family member 12 [Gene - OMIM - HGNC]
ORM1:orosomucoid 1 [Gene - OMIM - HGNC]
ORM2:orosomucoid 2 [Gene - OMIM - HGNC]
TMEM268:transmembrane protein 268 [Gene - HGNC]
WHRN:whirlin [Gene - OMIM - HGNC]
ZNF618:zinc finger protein 618 [Gene - OMIM - HGNC]

Variant type:

copy number loss

Cytogenetic location:

9q32

Genomic location:

Chr9: 116642144 - 117613527 (on Assembly GRCh37)

Preferred name:

GRCh37/hg19 9q32(chr9:116642144-117613527)x1

HGVS:

NC_000009.11:g.(?_116642144)_(117613527_?)del

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: CN517202

Recent activity

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cytochrome b, partial (mitochondrion) [Parastrellus hesperus]
cytochrome b, partial (mitochondrion) [Parastrellus hesperus]
gi|89892326|gb|ABD78937.1|

Protein

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001165813	Quest Diagnostics Nichols Institute San Juan Capistrano	no assertion criteria provided	Uncertain significance (Dec 10, 2018)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001165813

Quest Diagnostics Nichols Institute San Juan Capistrano

no assertion criteria provided

Uncertain significance
(Dec 10, 2018)

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, SCV001165813.1

#	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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