Gene: SERPINB7 (serpin family B member 7) Homo sapiens

Analyze

Symbol:

SERPINB7

Name:

serpin family B member 7

RGD ID:

736732

HGNC Page

HGNC:13902

Description:

Predicted to enable serine-type endopeptidase inhibitor activity. Predicted to be involved in positive regulation of collagen biosynthetic process; positive regulation of cytokine production; and positive regulation of glomerular mesangial cell proliferation. Predicted to be located in cytoplasm. Predicted to be active in obsolete extracellular space. Implicated in IgA glomerulonephritis; Nagashima-type palmoplantar keratosis; and familial encephalopathy with neuroserpin inclusion bodies.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

DKFZp686D06190; MEGSIN; mesangium predominant gene, megsin; MGC120014; MGC120015; PPKN; serine (or cysteine) proteinase inhibitor, clade B (ovalbumin), member 7; serpin B7; serpin peptidase inhibitor, clade B (ovalbumin), member 7; TP55

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Serpinb7 (serine (or cysteine) peptidase inhibitor, clade B, member 7)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, PhylomeDB
Rattus norvegicus (Norway rat):	Serpinb7 (serpin family B member 7)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoMCL, Panther, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Serpinb7 (serpin family B member 7)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	SERPINB7 (serpin family B member 7)	NCBI	Ortholog
Canis lupus familiaris (dog):	SERPINB7 (serpin family B member 7)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoMCL, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Serpinb7 (serpin family B member 7)	NCBI	Ortholog
Sus scrofa (pig):	SERPINB7 (serpin family B member 7)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	SERPINB7 (serpin family B member 7)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Serpinb7 (serpin family B member 7)	NCBI	Ortholog
Rattus rattus (black rat):	Serpinb7 (serpin family B member 7)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Cfap36 (cilia and flagella associated protein 36)	HGNC	OMA
Alliance orthologs ³
Mus musculus (house mouse):	Serpinb7 (serine (or cysteine) peptidase inhibitor, clade B, member 7)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Rattus norvegicus (Norway rat):	Serpinb7 (serpin family B member 7)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Drosophila melanogaster (fruit fly):	Spn28B	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	Spn27A	Alliance	DIOPT (Ensembl Compara\|OMA\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	Spn38F	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	Spn31A	Alliance	DIOPT (Ensembl Compara\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	nec	Alliance	DIOPT (Ensembl Compara\|OMA\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	Spn28Da	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	Spn28Db	Alliance	DIOPT (Ensembl Compara\|OMA\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	Spn28F	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	Spn42Dc	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|OMA\|PANTHER)
Drosophila melanogaster (fruit fly):	Spn42Dd	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoInspector\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	Spn43Aa	Alliance	DIOPT (Ensembl Compara\|OMA\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	Spn47C	Alliance	DIOPT (Ensembl Compara\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	Spn53F	Alliance	DIOPT (Ensembl Compara\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	Spn88Ea	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER\|SonicParanoid)
Drosophila melanogaster (fruit fly):	Spn88Eb	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER\|SonicParanoid)
Caenorhabditis elegans (roundworm):	srp-8	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|PANTHER\|PhylomeDB\|SonicParanoid)
Caenorhabditis elegans (roundworm):	srp-7	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus tropicalis (tropical clawed frog):	serpinb4	Alliance	DIOPT (OrthoFinder\|PANTHER\|PhylomeDB)

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	18	63,753,057 - 63,805,370 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	18	63,752,935 - 63,805,376 (+)	Ensembl		GRCh38.p14 Ensembl	hg38	GRCh38
GRCh37	18	61,420,291 - 61,472,604 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	18	59,571,257 - 59,623,584 (+)	NCBI	Build 36	Build 36	hg18	NCBI36
Build 34	18	59,593,623 - 59,623,590	NCBI
Celera	18	58,140,787 - 58,193,062 (+)	NCBI		Celera
Cytogenetic Map	18	q21.33	NCBI
HuRef	18	58,121,598 - 58,173,856 (+)	NCBI		HuRef
CHM1_1	18	61,416,473 - 61,468,833 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	18	63,958,110 - 64,010,475 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

Breast Cancer, Familial (IAGP)

cervical cancer (IAGP)

Diabetic Nephropathies (IAGP,IMP)

familial encephalopathy with neuroserpin inclusion bodies (IMP)

genetic disease (IAGP)

IgA glomerulonephritis (IAGP)

lung cancer (IAGP)

Nagashima-type palmoplantar keratosis (IAGP)

nephritis (ISO)

ovarian serous cystadenocarcinoma (IAGP)

palmoplantar keratosis (IAGP)

uterine corpus endometrial carcinoma (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

17beta-estradiol (EXP)

2-palmitoylglycerol (EXP)

4-nitrophenol (ISO)

6-propyl-2-thiouracil (ISO)

aflatoxin B1 (EXP)

amitrole (ISO)

ammonium chloride (ISO)

aristolochic acid A (EXP)

atrazine (ISO)

benzo[a]pyrene (EXP)

benzo[a]pyrene diol epoxide I (EXP)

Benzo[k]fluoranthene (ISO)

bis(2-chloroethyl) sulfide (EXP)

bisphenol A (EXP,ISO)

cadmium dichloride (EXP,ISO)

camptothecin (EXP)

CGP 52608 (EXP)

chlorohydrocarbon (ISO)

chlorpyrifos (ISO)

chromium(6+) (EXP)

cisplatin (EXP)

Cuprizon (ISO)

DDE (EXP)

dimethylarsinous acid (EXP)

doxorubicin (EXP)

flavonoids (ISO)

formaldehyde (EXP)

fulvestrant (EXP)

gentamycin (ISO)

imidacloprid (ISO)

lipopolysaccharide (EXP)

methimazole (ISO)

methylisothiazolinone (EXP)

methylmercury chloride (ISO)

mono(2-ethylhexyl) phthalate (EXP)

nickel sulfate (EXP)

okadaic acid (EXP)

paraquat (ISO)

perfluorooctane-1-sulfonic acid (EXP)

potassium chromate (EXP)

S-(1,2-dichlorovinyl)-L-cysteine (EXP)

silicon dioxide (EXP)

sodium arsenite (EXP)

sulfadimethoxine (ISO)

temozolomide (EXP)

trichloroethene (ISO)

zoledronic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

positive regulation of collagen biosynthetic process (IEA,ISO)

positive regulation of glomerular mesangial cell proliferation (IEA,ISO)

positive regulation of platelet-derived growth factor production (IEA,ISO)

positive regulation of transforming growth factor beta1 production (IEA,ISO)

Cellular Component

cytoplasm (IEA)

extracellular region (IBA,IEA)

Molecular Function

serine-type endopeptidase inhibitor activity (IBA,IEA,TAS)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Autosomal recessive inheritance (IAGP)

Childhood onset (IAGP)

Congenital onset (IAGP)

Epidermal acanthosis (IAGP)

Hypergranulosis (IAGP)

Hyperhidrosis (IAGP)

Infantile onset (IAGP)

Juvenile onset (IAGP)

Maceration (IAGP)

Neonatal onset (IAGP)

Neoplasm of the lung (IAGP)

Orthokeratotic hyperkeratosis (IAGP)

Palmoplantar hyperhidrosis (IAGP)

Palmoplantar hyperkeratosis (IAGP)

Palmoplantar keratoderma (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	A severe diabetic nephropathy model with early development of nodule-like lesions induced by megsin overexpression in RAGE/iNOS transgenic mice.	Inagi R, etal., Diabetes. 2006 Feb;55(2):356-66.
3.	Megsin 2093T-2180C haplotype at the 3' untranslated region is associated with poor renal survival in Korean IgA nephropathy patients.	Lim CS, etal., Clin Nephrol. 2008 Aug;70(2):101-9.
4.	Genetic analysis of diabetic nephropathy on chromosome 18 in African Americans: linkage analysis and dense SNP mapping.	McDonough CW, etal., Hum Genet. 2009 Dec;126(6):805-17. doi: 10.1007/s00439-009-0732-8.
5.	Cloning of rodent megsin revealed its up-regulation in mesangioproliferative nephritis.	Nangaku M, etal., Kidney Int 2001 Aug;60(2):641-52.
6.	OMIM Disease Annotation Pipeline	OMIM Disease Annotation Pipeline
7.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
8.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions
9.	RGD HPO Phenotype Annotation Pipeline	RGD automated import pipeline for human HPO-to-gene-to-disease annotations
10.	A rat model of human FENIB (familial encephalopathy with neuroserpin inclusion bodies).	Takano K, etal., Biochem Biophys Res Commun. 2006 Aug 4;346(3):1040-7. Epub 2006 Jun 12.
11.	[Association of single nucleotide polymorphism of megsin gene with IgA nephropathy].	Wang ZH, etal., Zhonghua Yi Xue Za Zhi. 2006 May 23;86(19):1337-41.
12.	A family-based association study of megsin A23167G polymorphism with susceptibility and progression of IgA nephropathy in a Chinese population.	Xia YF, etal., Clin Nephrol. 2006 Mar;65(3):153-9.

Additional References at PubMed

PMID:9182567	PMID:9710452	PMID:10589701	PMID:11527413	PMID:11877466	PMID:12386281	PMID:12397041	PMID:12477932	PMID:15213261	PMID:15342556	PMID:15489334	PMID:15788472
PMID:16344560	PMID:16431886	PMID:18471408	PMID:18498720	PMID:18580857	PMID:19403671	PMID:20628624	PMID:21873635	PMID:21993616	PMID:23383108	PMID:24172014	PMID:24207119
PMID:24514002	PMID:24575807	PMID:24773080	PMID:24954659	PMID:25007157	PMID:25940237	PMID:26186194	PMID:26763456	PMID:26871801	PMID:26949251	PMID:27666198	PMID:27786350
PMID:28211129	PMID:28514442	PMID:29106929	PMID:29987050	PMID:30592269	PMID:31706940	PMID:32406097	PMID:33961781	PMID:34334259	PMID:34379845	PMID:34383978	PMID:34454985
PMID:34732716	PMID:35178744	PMID:35864103	PMID:36215168	PMID:36772997	PMID:37314216	PMID:37935254	PMID:38529670

Genomics

Comparative Map Data

SERPINB7
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	18	63,753,057 - 63,805,370 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	18	63,752,935 - 63,805,376 (+)	Ensembl		GRCh38.p14 Ensembl	hg38	GRCh38
GRCh37	18	61,420,291 - 61,472,604 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	18	59,571,257 - 59,623,584 (+)	NCBI	Build 36	Build 36	hg18	NCBI36
Build 34	18	59,593,623 - 59,623,590	NCBI
Celera	18	58,140,787 - 58,193,062 (+)	NCBI		Celera
Cytogenetic Map	18	q21.33	NCBI
HuRef	18	58,121,598 - 58,173,856 (+)	NCBI		HuRef
CHM1_1	18	61,416,473 - 61,468,833 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	18	63,958,110 - 64,010,475 (+)	NCBI		T2T-CHM13v2.0

Serpinb7
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	1	107,350,418 - 107,380,419 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	1	107,327,385 - 107,380,419 (+)	Ensembl		GRCm39 Ensembl		GRCm39
GRCm38	1	107,422,689 - 107,452,689 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	1	107,399,655 - 107,452,689 (+)	Ensembl		GRCm38.p6 Ensembl	mm10	GRCm38
MGSCv37	1	109,319,266 - 109,349,266 (+)	NCBI	MGSCv37	MGSCv37	mm9	NCBIm37
MGSCv36	1	109,250,236 - 109,280,235 (+)	NCBI		MGSCv36	mm8
Celera	1	110,260,443 - 110,291,388 (+)	NCBI		Celera
Cytogenetic Map	1	E2.1	NCBI
cM Map	1	50.34	NCBI

Serpinb7
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	13	23,884,466 - 23,956,834 (+)	NCBI	GRCr8	GRCr8		GRCr8
GRCr8 Ensembl	13	23,910,306 - 23,956,834 (+)	Ensembl				GRCr8
mRatBN7.2	13	23,369,830 - 23,442,205 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	13	23,395,671 - 23,442,205 (+)	Ensembl				mRatBN7.2
UTH_Rnor_SHR_Utx	13	23,770,062 - 23,811,605 (+)	NCBI	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	13	25,054,524 - 25,096,071 (+)	NCBI	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	13	23,740,244 - 23,781,790 (+)	NCBI	UTH_Rnor_WKY_Bbb_1.0
Dahl_SR_JrHsd	13	23,639,094 - 23,685,612 (+)	NCBI
Lyon_Normotensive	13	23,638,487 - 23,685,005 (+)	NCBI
Lyon_Hypertensive	13	23,652,391 - 23,698,905 (+)	NCBI
F344_StmMcwi	13	23,558,913 - 23,605,427 (+)	NCBI
Rnor_6.0	13	27,282,456 - 27,354,775 (+)	NCBI	Rnor_6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	13	27,312,498 - 27,354,052 (+)	Ensembl		Rnor_6.0 Ensembl	rn6	Rnor6.0
Rnor_5.0	13	32,431,704 - 32,503,907 (+)	NCBI	Rnor_5.0	Rnor_5.0	rn5
RGSC_v3.4	13	13,464,818 - 13,506,372 (+)	NCBI	RGSC_v3.4	RGSC_v3.4	rn4
Celera	13	23,245,098 - 23,286,663 (+)	NCBI		Celera
RGSC_v3.1	13	13,464,817 - 13,506,372 (+)	NCBI
Cytogenetic Map	13	p11	NCBI

Serpinb7
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0 Ensembl	NW_004955402	47,599,150 - 47,649,885 (+)	Ensembl		ChiLan1.0 Ensembl
ChiLan1.0	NW_004955402	47,599,503 - 47,649,537 (+)	NCBI	ChiLan1.0	ChiLan1.0

SERPINB7
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	17	81,269,142 - 81,315,895 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	18	66,956,410 - 67,008,506 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	18	57,112,242 - 57,164,213 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	18	60,423,119 - 60,475,171 (+)	NCBI	PanPan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	18	60,445,135 - 60,475,165 (+)	Ensembl		PanPan1.1 Ensembl	panPan2	panpan1.1

SERPINB7
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	1	13,336,067 - 13,392,674 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	1	13,336,837 - 13,358,125 (-)	Ensembl		CanFam3.1 Ensembl	canFam3	CanFam3.1
Dog10K_Boxer_Tasha	1	14,296,781 - 14,353,408 (-)	NCBI	Dog10K_Boxer_Tasha	Dog10K_Boxer_Tasha
ROS_Cfam_1.0	1	13,191,171 - 13,247,792 (-)	NCBI	ROS_Cfam_1.0	ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	1	13,191,169 - 13,218,577 (-)	Ensembl				ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	1	13,229,696 - 13,286,210 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	1	13,158,947 - 13,215,544 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	1	13,408,033 - 13,464,630 (-)	NCBI	UU_Cfam_GSD_1.0	UU_Cfam_GSD_1.0

Serpinb7
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
mIctTri1.hap1	13	12,274,899 - 12,327,031 (-)	NCBI		mIctTri1.hap1
HiC_Itri_2	NW_024404944	26,626,496 - 26,678,824 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936497	1,866,166 - 1,887,690 (-)	Ensembl		SpeTri2.0 Ensembl
SpeTri2.0	NW_004936497	1,865,540 - 1,887,695 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

SERPINB7
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	1	157,953,877 - 157,998,842 (-)	Ensembl		Sscrofa11.1 Ensembl	susScr11	Sscrofa11.1
Sscrofa11.1	1	157,953,872 - 157,999,242 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	1	175,390,325 - 175,435,317 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

SERPINB7
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
mChlSab1.0.hap1	18	16,644,539 - 16,672,552 (-)	NCBI		mChlSab1.0.hap1
Vero_WHO_p1.0	NW_023666060	9,672,358 - 9,700,689 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0
ChlSab1.1	18	15,992,154 - 16,020,001 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	18	15,992,186 - 16,044,650 (-)	Ensembl		ChlSab1.1 Ensembl	chlSab2	Vervet-AGM

Serpinb7
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla 1.0	NW_004624792	9,730,223 - 9,794,673 (+)	NCBI	HetGla 1.0	HetGla 1.0	hetGla2

Serpinb7
(Rattus rattus - black rat)

Black Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Black Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Rrattus_CSIRO_v1	4	119,607,878 - 119,643,230 (-)	NCBI	Rrattus_CSIRO_v1	Rrattus_CSIRO_v1

Variants

Variants in SERPINB7
88 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
NM_003784.4(SERPINB7):c.218_219delinsTAAACTTTACCT (p.Gln73fs)	indel	PALMOPLANTAR KERATODERMA, NAGASHIMA TYPE [RCV000088683]	Chr18:63792442..63792443 [GRCh38] Chr18:61459676..61459677 [GRCh37] Chr18:18q21.33	pathogenic
NM_003784.4(SERPINB7):c.455-1G>A	single nucleotide variant	PALMOPLANTAR KERATODERMA, NAGASHIMA TYPE [RCV000088684]	Chr18:63798603 [GRCh38] Chr18:61465837 [GRCh37] Chr18:18q21.33	pathogenic
NM_003784.4(SERPINB7):c.796C>T (p.Arg266Ter)	single nucleotide variant	Palmoplantar keratodermas [RCV000088682]	Chr18:63804288 [GRCh38] Chr18:61471522 [GRCh37] Chr18:18q21.33	pathogenic
GRCh38/hg38 18q21.1-23(chr18:50068129-80252149)x3	copy number gain	Intellectual disability [RCV000050989]	Chr18:18q21.1-23	pathogenic
GRCh38/hg38 18q21.31-23(chr18:56618038-80252149)x1	copy number loss	Abnormality of the nervous system [RCV000051032]	Chr18:18q21.31-23	pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80252149)x3	copy number gain	Hydrocephalus [RCV000051048]	Chr18:18p11.32-q23	pathogenic
GRCh38/hg38 18q11.1-23(chr18:20960320-80234429)x3	copy number gain	Wide intermamillary distance [RCV000052543]	Chr18:18q11.1-23	pathogenic
GRCh38/hg38 18p11.32-q23(chr18:53345-80209986)x3	copy number gain	Cataract [RCV000052501]	Chr18:18p11.32-q23	pathogenic
GRCh38/hg38 18q11.1-23(chr18:20989762-80209986)x3	copy number gain	See cases [RCV000052549]	Chr18:18q11.1-23	pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148763-80252290)x3	copy number gain	See cases [RCV000052507]	Chr18:148763..80252290 [GRCh38] Chr18:148763..78010173 [GRCh37] Chr18:138763..76111164 [NCBI36] Chr18:18p11.32-q23	pathogenic
GRCh38/hg38 18q12.1-22.1(chr18:29249202-65448117)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052563]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052563]\|See cases [RCV000052563]	Chr18:29249202..65448117 [GRCh38] Chr18:26829167..63115353 [GRCh37] Chr18:25083165..61266333 [NCBI36] Chr18:18q12.1-22.1	pathogenic
GRCh38/hg38 18q21.2-23(chr18:53637007-80252149)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053869]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053869]\|See cases [RCV000053869]	Chr18:53637007..80252149 [GRCh38] Chr18:51163377..78010032 [GRCh37] Chr18:49417375..76111023 [NCBI36] Chr18:18q21.2-23	pathogenic
GRCh38/hg38 18q21.31-23(chr18:56353040-80209986)x1	copy number loss	Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000053873]	Chr18:18q21.31-23	pathogenic
GRCh38/hg38 18q21.2-23(chr18:51605752-80252149)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053834]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053834]\|See cases [RCV000053834]	Chr18:51605752..80252149 [GRCh38] Chr18:49132122..78010032 [GRCh37] Chr18:47386120..76111023 [NCBI36] Chr18:18q21.2-23	pathogenic
GRCh38/hg38 18q21.2-22.1(chr18:52156899-65408762)x1	copy number loss	See cases [RCV000053836]	Chr18:18q21.2-22.1	pathogenic
NM_001040147.2(SERPINB7):c.1119C>T (p.Phe373=)	single nucleotide variant	Malignant melanoma [RCV000071875]	Chr18:63804611 [GRCh38] Chr18:61471845 [GRCh37] Chr18:59622825 [NCBI36] Chr18:18q21.33	not provided
GRCh38/hg38 18q21.32-23(chr18:59567681-80252149)x1	copy number loss	Abnormality of cardiac morphology [RCV000133689]	Chr18:18q21.32-23	pathogenic
NM_003784.4(SERPINB7):c.522dup (p.Val175fs)	duplication	PALMOPLANTAR KERATODERMA, NAGASHIMA TYPE [RCV000144910]	Chr18:63798670..63798671 [GRCh38] Chr18:61465904..61465905 [GRCh37] Chr18:18q21.33	pathogenic\|not provided
GRCh38/hg38 18p11.32-q23(chr18:149089-80234391)x3	copy number gain	See cases [RCV000134110]	Chr18:18p11.32-q23	pathogenic
GRCh38/hg38 18q21.33-23(chr18:63306200-80252149)x1	copy number loss	Global developmental delay [RCV000135838]	Chr18:18q21.33-23	pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80244381)x3	copy number gain	Global developmental delay [RCV000052514]	Chr18:18p11.32-q23	pathogenic
GRCh38/hg38 18q21.33-23(chr18:63195579-80234429)x3	copy number gain	Hydronephrosis [RCV000052572]	Chr18:18q21.33-23	pathogenic
GRCh38/hg38 18q21.33-23(chr18:62999696-80209986)x1	copy number loss	Global developmental delay [RCV000053875]	Chr18:18q21.33-23	pathogenic
GRCh38/hg38 18q21.33-23(chr18:61576009-80252149)x1	copy number loss	Microcephaly [RCV000135616]	Chr18:18q21.33-23	pathogenic
GRCh38/hg38 18q21.2-23(chr18:51190429-80252149)x1	copy number loss	See cases [RCV000135413]	Chr18:18q21.2-23	pathogenic
GRCh38/hg38 18q21.33-23(chr18:61827111-80252149)x1	copy number loss	See cases [RCV000135567]	Chr18:18q21.33-23	pathogenic\|uncertain significance
GRCh38/hg38 18q12.1-23(chr18:32123105-80252149)x3	copy number gain	See cases [RCV000136890]	Chr18:18q12.1-23	pathogenic
GRCh38/hg38 18q21.2-23(chr18:53865057-80252149)x1	copy number loss	Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000136674]	Chr18:18q21.2-23	pathogenic
GRCh38/hg38 18q21.1-23(chr18:49199411-80254946)x3	copy number gain	Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000137342]	Chr18:18q21.1-23	pathogenic
GRCh38/hg38 18q21.2-23(chr18:55179364-80254946)x1	copy number loss	Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000137375]	Chr18:18q21.2-23	pathogenic
GRCh38/hg38 18q12.3-23(chr18:42651392-80254946)x3	copy number gain	Delayed speech and language development [RCV000138034]	Chr18:18q12.3-23	pathogenic
GRCh38/hg38 18p11.32-q23(chr18:149089-80254936)x3	copy number gain	See cases [RCV000139397]	Chr18:18p11.32-q23	pathogenic
GRCh38/hg38 18q21.2-23(chr18:52421052-80254946)x1	copy number loss	See cases [RCV000139134]	Chr18:18q21.2-23	pathogenic
GRCh38/hg38 18q21.2-23(chr18:53959828-80254936)x3	copy number gain	Nail dysplasia [RCV000139496]	Chr18:18q21.2-23	pathogenic
GRCh38/hg38 18q21.33-23(chr18:63756916-80254946)x1	copy number loss	See cases [RCV000139464]	Chr18:18q21.33-23	pathogenic
GRCh38/hg38 18q21.33-23(chr18:61613338-80252090)x1	copy number loss	Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000141429]	Chr18:18q21.33-23	pathogenic
GRCh38/hg38 18q21.2-23(chr18:51167159-80256240)x1	copy number loss	Incoordination [RCV000140925]	Chr18:18q21.2-23	pathogenic
GRCh38/hg38 18p11.32-q23(chr18:136227-80256240)x3	copy number gain	Intrauterine growth retardation [RCV000142244]	Chr18:18p11.32-q23	pathogenic
GRCh38/hg38 18q11.1-22.3(chr18:20962119-74691446)x3	copy number gain	See cases [RCV000143057]	Chr18:18q11.1-22.3	pathogenic
GRCh37/hg19 18p11.32-q23(chr18:163323-78005236)x3	copy number gain	Abnormality of the fetal cardiovascular system [RCV000240130]	Chr18:18p11.32-q23	pathogenic
GRCh37/hg19 18q21.32-22.2(chr18:58014591-68158862)x1	copy number loss	Renal agenesis [RCV000240432]	Chr18:18q21.32-22.2	pathogenic
GRCh37/hg19 18q21.32-23(chr18:58525322-78005236)x3	copy number gain	Global developmental delay [RCV000240296]	Chr18:18q21.32-23	pathogenic
GRCh37/hg19 18q21.33-23(chr18:59461447-78010032)x1	copy number loss	not provided [RCV000416006]	Chr18:18q21.33-23	likely pathogenic
GRCh37/hg19 18q21.31-22.3(chr18:55793243-68705548)x1	copy number loss	See cases [RCV000449209]	Chr18:55793243..68705548 [GRCh37] Chr18:18q21.31-22.3	pathogenic
GRCh37/hg19 18q21.2-22.1(chr18:50739715-63705988)x1	copy number loss	See cases [RCV000446087]	Chr18:50739715..63705988 [GRCh37] Chr18:18q21.2-22.1	pathogenic
GRCh37/hg19 18q21.33-23(chr18:60641553-78014123)x1	copy number loss	See cases [RCV000447127]	Chr18:60641553..78014123 [GRCh37] Chr18:18q21.33-23	pathogenic
GRCh37/hg19 18q21.33-23(chr18:60796196-78014123)x1	copy number loss	See cases [RCV000446171]	Chr18:60796196..78014123 [GRCh37] Chr18:18q21.33-23	pathogenic
GRCh37/hg19 18q21.33-22.1(chr18:61249958-62516230)x3	copy number gain	See cases [RCV000445966]	Chr18:61249958..62516230 [GRCh37] Chr18:18q21.33-22.1	likely benign
GRCh37/hg19 18q21.2-23(chr18:53100584-78014123)x1	copy number loss	See cases [RCV000445943]	Chr18:53100584..78014123 [GRCh37] Chr18:18q21.2-23	pathogenic
GRCh37/hg19 18q21.2-23(chr18:52837852-77989426)x1	copy number loss	See cases [RCV000448656]	Chr18:52837852..77989426 [GRCh37] Chr18:18q21.2-23	pathogenic
GRCh37/hg19 18q21.31-23(chr18:54462182-78014123)x1	copy number loss	See cases [RCV000512059]	Chr18:18q21.31-23	pathogenic
GRCh37/hg19 18q21.33-23(chr18:59809990-78014123)x1	copy number loss	Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000510685]	Chr18:18q21.33-23	pathogenic
GRCh37/hg19 18q11.1-22.1(chr18:18521285-64495798)x3	copy number gain	See cases [RCV000511734]	Chr18:18q11.1-22.1	pathogenic
GRCh37/hg19 18p11.21-q23(chr18:14869204-78014123)x3	copy number gain	Short stature [RCV000512030]	Chr18:18p11.21-q23	pathogenic
GRCh37/hg19 18q21.1-23(chr18:46177798-78014123)x1	copy number loss	Cleft palate [RCV000511759]	Chr18:18q21.1-23	pathogenic
GRCh37/hg19 18q21.32-23(chr18:58768873-78014123)x1	copy number loss	See cases [RCV000512579]	Chr18:18q21.32-23	pathogenic
GRCh37/hg19 18q21.31-22.3(chr18:55083032-72743857)x1	copy number loss	not provided [RCV000684056]	Chr18:18q21.31-22.3	pathogenic
GRCh37/hg19 18q21.31-23(chr18:55298900-78014123)x1	copy number loss	not provided [RCV000684059]	Chr18:18q21.31-23	pathogenic
GRCh37/hg19 18q21.1-23(chr18:46942427-78014123)x1	copy number loss	not provided [RCV000684060]	Chr18:18q21.1-23	pathogenic
GRCh37/hg19 18q21.32-23(chr18:56905884-78014123)x1	copy number loss	not provided [RCV000684058]	Chr18:18q21.32-23	pathogenic
GRCh37/hg19 18q21.2-23(chr18:52802515-78015180)x1	copy number loss	not provided [RCV000739824]	Chr18:52802515..78015180 [GRCh37] Chr18:18q21.2-23	pathogenic
NM_003784.4(SERPINB7):c.597+78T>C	single nucleotide variant	Not Provided [RCV001611265]	Chr18:63798824 [GRCh38] Chr18:61466058 [GRCh37] Chr18:18q21.33	benign
NM_003784.4(SERPINB7):c.797G>A (p.Arg266Gln)	single nucleotide variant	Not Provided [RCV001613467]	Chr18:63804289 [GRCh38] Chr18:61471523 [GRCh37] Chr18:18q21.33	benign
GRCh37/hg19 18p11.32-q23(chr18:12842-78015180)x3	copy number gain	not provided [RCV000752245]	Chr18:12842..78015180 [GRCh37] Chr18:18p11.32-q23	pathogenic
GRCh37/hg19 18q21.32-22.1(chr18:57244903-63722436)x1	copy number loss	not provided [RCV000752355]	Chr18:57244903..63722436 [GRCh37] Chr18:18q21.32-22.1	benign
GRCh37/hg19 18q21.32-23(chr18:57244903-77325446)x1	copy number loss	not provided [RCV000752356]	Chr18:57244903..77325446 [GRCh37] Chr18:18q21.32-23	pathogenic
NM_003784.4(SERPINB7):c.1136G>A (p.Cys379Tyr)	single nucleotide variant	not provided [RCV000996696]	Chr18:63804628 [GRCh38] Chr18:61471862 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.986T>G (p.Val329Gly)	single nucleotide variant	not provided [RCV001091659]	Chr18:63804478 [GRCh38] Chr18:61471712 [GRCh37] Chr18:18q21.33	uncertain significance
GRCh37/hg19 18q21.31-23(chr18:55458425-78014123)x1	copy number loss	not provided [RCV001007017]	Chr18:18q21.31-23	pathogenic
NM_003784.4(SERPINB7):c.310G>C (p.Ala104Pro)	single nucleotide variant	Inborn genetic diseases [RCV003290807]	Chr18:63793251 [GRCh38] Chr18:61460485 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.169-261G>A	single nucleotide variant	Not Provided [RCV001685261]	Chr18:63792132 [GRCh38] Chr18:61459366 [GRCh37] Chr18:18q21.33	benign
NM_003784.4(SERPINB7):c.598-15T>A	single nucleotide variant	Not Provided [RCV001693838]	Chr18:63800851 [GRCh38] Chr18:61468085 [GRCh37] Chr18:18q21.33	benign\|evidence_only
NM_003784.4(SERPINB7):c.169-211A>G	single nucleotide variant	Not Provided [RCV001621170]	Chr18:63792182 [GRCh38] Chr18:63792182..63792183 [GRCh38] Chr18:61459416 [GRCh37] Chr18:61459416..61459417 [GRCh37] Chr18:18q21.33	benign
NM_003784.4(SERPINB7):c.744+60G>C	single nucleotide variant	not provided [RCV001694956]	Chr18:63801072 [GRCh38] Chr18:61468306 [GRCh37] Chr18:18q21.33	benign
GRCh37/hg19 18q21.32-23(chr18:56750525-78014123)x1	copy number loss	not provided [RCV001007018]	Chr18:18q21.32-23	pathogenic
NM_003784.4(SERPINB7):c.597+44C>T	single nucleotide variant	Not Provided [RCV001684485]	Chr18:63798790 [GRCh38] Chr18:61466024 [GRCh37] Chr18:18q21.33	benign
GRCh37/hg19 18q21.31-23(chr18:54285235-77960815)x1	copy number loss	not provided [RCV001531449]	Chr18:18q21.31-23	pathogenic
NM_003784.4(SERPINB7):c.65A>G (p.Asn22Ser)	single nucleotide variant	Inborn genetic diseases [RCV005488901]	Chr18:63782437 [GRCh38] Chr18:61449671 [GRCh37] Chr18:18q21.33	likely benign
NM_003784.4(SERPINB7):c.128G>A (p.Arg43His)	single nucleotide variant	Inborn genetic diseases [RCV006371653]	Chr18:63782500 [GRCh38] Chr18:61449734 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.529T>C (p.Phe177Leu)	single nucleotide variant	Inborn genetic diseases [RCV006371659]	Chr18:63798678 [GRCh38] Chr18:61465912 [GRCh37] Chr18:18q21.33	uncertain significance
Single allele	deletion	Deletion of long arm of chromosome 18 [RCV002280357]	Chr18:61490305..80247612 [GRCh38] Chr18:18q21.33-23	pathogenic
NM_003784.4(SERPINB7):c.650_653del (p.Ser217fs)	deletion	Palmoplantar keratoderma, Nagashima type [RCV001807885]	Chr18:63800915..63800918 [GRCh38] Chr18:61468149..61468152 [GRCh37] Chr18:18q21.33	pathogenic
NM_003784.4(SERPINB7):c.455-28A>G	single nucleotide variant	Not Provided [RCV001710880]	Chr18:63798576 [GRCh38] Chr18:61465810 [GRCh37] Chr18:18q21.33	benign
NM_003784.4(SERPINB7):c.220-109A>T	single nucleotide variant	Not Provided [RCV001617894]	Chr18:63793052 [GRCh38] Chr18:61460286 [GRCh37] Chr18:18q21.33	benign
NM_003784.4(SERPINB7):c.454+167G>T	single nucleotide variant	not provided [RCV001710717]	Chr18:63796550 [GRCh38] Chr18:61463784 [GRCh37] Chr18:18q21.33	benign
NM_003784.4(SERPINB7):c.157C>T (p.Gln53Ter)	single nucleotide variant	Palmoplantar keratoderma, Nagashima type [RCV001784959]	Chr18:63782529 [GRCh38] Chr18:61449763 [GRCh37] Chr18:18q21.33	pathogenic
GRCh37/hg19 18q21.2-23(chr18:53309113-78014123)	copy number loss	not specified [RCV002052646]	Chr18:18q21.2-23	pathogenic
GRCh37/hg19 18q21.33-23(chr18:59332806-78014123)	copy number loss	not specified [RCV002052649]	Chr18:18q21.33-23	pathogenic
GRCh37/hg19 18p11.32-q23(chr18:136226-78014123)	copy number gain	not specified [RCV002052616]	Chr18:18p11.32-q23	pathogenic
GRCh37/hg19 18q21.2-23(chr18:53100584-78014123)	copy number loss	not specified [RCV002052643]	Chr18:18q21.2-23	pathogenic
GRCh37/hg19 18q21.32-23(chr18:58305972-78014123)	copy number loss	not specified [RCV002052647]	Chr18:18q21.32-23	pathogenic
GRCh37/hg19 18q21.2-23(chr18:52837852-77989426)	copy number loss	not specified [RCV002052642]	Chr18:18q21.2-23	pathogenic
NC_000018.9:g.(?_59713089)_(61654512_?)del	deletion	Multiple congenital anomalies-hypotonia-seizures syndrome 1 [RCV001898809]	Chr18:18q21.33-22.1	pathogenic\|no classifications from unflagged records
NM_003784.4(SERPINB7):c.1135T>C (p.Cys379Arg)	single nucleotide variant	not provided [RCV001897110]	Chr18:63804627 [GRCh38] Chr18:61471861 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.992A>C (p.Glu331Ala)	single nucleotide variant	not provided [RCV001883551]	Chr18:63804484 [GRCh38] Chr18:61471718 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.803C>T (p.Thr268Ile)	single nucleotide variant	not provided [RCV002125058]	Chr18:63804295 [GRCh38] Chr18:61471529 [GRCh37] Chr18:18q21.33	benign
NM_003784.4(SERPINB7):c.366C>T (p.Tyr122=)	single nucleotide variant	not provided [RCV002206859]	Chr18:63796295 [GRCh38] Chr18:61463529 [GRCh37] Chr18:18q21.33	likely benign
NM_003784.4(SERPINB7):c.455-7dup	duplication	not provided [RCV002103469]	Chr18:63798588..63798589 [GRCh38] Chr18:61465822..61465823 [GRCh37] Chr18:18q21.33	benign
NM_003784.4(SERPINB7):c.745-19C>G	single nucleotide variant	not provided [RCV002082252]	Chr18:63804218 [GRCh38] Chr18:61471452 [GRCh37] Chr18:18q21.33	benign
NM_003784.4(SERPINB7):c.835T>G (p.Phe279Val)	single nucleotide variant	Inborn genetic diseases [RCV006371654]	Chr18:63804327 [GRCh38] Chr18:61471561 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.899T>C (p.Phe300Ser)	single nucleotide variant	Inborn genetic diseases [RCV006371656]	Chr18:63804391 [GRCh38] Chr18:61471625 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.331C>A (p.His111Asn)	single nucleotide variant	Inborn genetic diseases [RCV005488898]	Chr18:63793272 [GRCh38] Chr18:61460506 [GRCh37] Chr18:18q21.33	uncertain significance
GRCh37/hg19 18q21.33-23(chr18:61289055-78014123)	copy number loss	Deletion of long arm of chromosome 18 [RCV002280712]	Chr18:18q21.33-23	pathogenic
NM_003784.4(SERPINB7):c.637A>G (p.Lys213Glu)	single nucleotide variant	Inborn genetic diseases [RCV002687772]	Chr18:63800905 [GRCh38] Chr18:61468139 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.416G>C (p.Arg139Thr)	single nucleotide variant	Inborn genetic diseases [RCV002883931]	Chr18:63796345 [GRCh38] Chr18:61463579 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.931G>A (p.Ala311Thr)	single nucleotide variant	Inborn genetic diseases [RCV002772813]	Chr18:63804423 [GRCh38] Chr18:61471657 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.634C>T (p.Arg212Trp)	single nucleotide variant	not provided [RCV002949326]	Chr18:63800902 [GRCh38] Chr18:61468136 [GRCh37] Chr18:18q21.33	likely benign
NM_003784.4(SERPINB7):c.715G>A (p.Val239Ile)	single nucleotide variant	not provided [RCV003077990]	Chr18:63800983 [GRCh38] Chr18:61468217 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.625C>A (p.His209Asn)	single nucleotide variant	Inborn genetic diseases [RCV002799370]	Chr18:63800893 [GRCh38] Chr18:61468127 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.181A>G (p.Asn61Asp)	single nucleotide variant	SERPINB7-related condition [RCV002917792]	Chr18:63792405 [GRCh38] Chr18:61459639 [GRCh37] Chr18:18q21.33	benign\|likely benign
NM_003784.4(SERPINB7):c.634C>G (p.Arg212Gly)	single nucleotide variant	Inborn genetic diseases [RCV002793146]	Chr18:63800902 [GRCh38] Chr18:61468136 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.565G>A (p.Glu189Lys)	single nucleotide variant	Inborn genetic diseases [RCV002674665]	Chr18:63798714 [GRCh38] Chr18:61465948 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.714C>T (p.Tyr238=)	single nucleotide variant	not provided [RCV002922173]	Chr18:63800982 [GRCh38] Chr18:61468216 [GRCh37] Chr18:18q21.33	likely benign
NM_003784.4(SERPINB7):c.611C>G (p.Ala204Gly)	single nucleotide variant	Inborn genetic diseases [RCV002920139]	Chr18:63800879 [GRCh38] Chr18:61468113 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.418C>T (p.Arg140Cys)	single nucleotide variant	Inborn genetic diseases [RCV002962148]	Chr18:63796347 [GRCh38] Chr18:61463581 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.877G>T (p.Ala293Ser)	single nucleotide variant	not provided [RCV003061291]	Chr18:63804369 [GRCh38] Chr18:61471603 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.220T>C (p.Ser74Pro)	single nucleotide variant	Inborn genetic diseases [RCV002606524]	Chr18:63793161 [GRCh38] Chr18:61460395 [GRCh37] Chr18:18q21.33	likely benign\|uncertain significance
NM_003784.4(SERPINB7):c.168G>T (p.Lys56Asn)	single nucleotide variant	not provided [RCV002610743]	Chr18:63782540 [GRCh38] Chr18:61449774 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.871T>A (p.Leu291Met)	single nucleotide variant	Inborn genetic diseases [RCV006371652]	Chr18:63804363 [GRCh38] Chr18:61471597 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.197A>T (p.Tyr66Phe)	single nucleotide variant	Inborn genetic diseases [RCV006371657]	Chr18:63792421 [GRCh38] Chr18:61459655 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.958A>G (p.Arg320Gly)	single nucleotide variant	Inborn genetic diseases [RCV006371658]	Chr18:63804450 [GRCh38] Chr18:61471684 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.896T>C (p.Ile299Thr)	single nucleotide variant	Inborn genetic diseases [RCV005488900]	Chr18:63804388 [GRCh38] Chr18:61471622 [GRCh37] Chr18:18q21.33	uncertain significance
GRCh37/hg19 18q21.2-22.2(chr18:52640210-68070259)x4	copy number gain	not provided [RCV006436470]	Chr18:18q21.2-22.2	pathogenic
GRCh37/hg19 18q21.33-22.1(chr18:61460244-62040101)x3	copy number gain	not provided [RCV006436477]	Chr18:18q21.33-22.1	uncertain significance
GRCh37/hg19 18q21.2-23(chr18:53564430-74587425)x1	copy number loss	not provided [RCV006436468]	Chr18:18q21.2-23	pathogenic
GRCh37/hg19 18q21.33-22.1(chr18:60440410-64199966)x1	copy number loss	not provided [RCV006436472]	Chr18:18q21.33-22.1	uncertain significance
GRCh37/hg19 18q21.33-22.1(chr18:60643748-64474178)x3	copy number gain	not provided [RCV006436490]	Chr18:18q21.33-22.1	uncertain significance
NM_003784.4(SERPINB7):c.50G>T (p.Arg17Ile)	single nucleotide variant	Uterine corpus endometrial carcinoma [RCV006128986]	Chr18:63782422 [GRCh38] Chr18:61449656 [GRCh37] Chr18:18q21.33	evidence_only
GRCh37/hg19 18q21.33-22.1(chr18:61388177-62025124)x1	copy number loss	not specified [RCV005627962]	Chr18:18q21.33-22.1	uncertain significance
NM_003784.4(SERPINB7):c.370G>A (p.Ala124Thr)	single nucleotide variant	Inborn genetic diseases [RCV006371655]	Chr18:63796299 [GRCh38] Chr18:61463533 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.920T>C (p.Leu307Pro)	single nucleotide variant	Inborn genetic diseases [RCV005488896]	Chr18:63804412 [GRCh38] Chr18:61471646 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.1139C>T (p.Pro380Leu)	single nucleotide variant	Inborn genetic diseases [RCV005488903]	Chr18:63804631 [GRCh38] Chr18:61471865 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.745-73G>T	single nucleotide variant	Lung cancer [RCV006128989]	Chr18:63804164 [GRCh38] Chr18:61471398 [GRCh37] Chr18:18q21.33	evidence_only
NM_003784.4(SERPINB7):c.650C>G (p.Ser217Cys)	single nucleotide variant	Inborn genetic diseases [RCV006680964]	Chr18:63800918 [GRCh38] Chr18:61468152 [GRCh37] Chr18:18q21.33	uncertain significance
GRCh37/hg19 18q21.33-23(chr18:60771809-78014123)x1	copy number loss	not provided [RCV003483341]	Chr18:18q21.33-23	pathogenic
NM_003784.4(SERPINB7):c.108C>T (p.Phe36=)	single nucleotide variant	not provided [RCV003413473]	Chr18:63782480 [GRCh38] Chr18:61449714 [GRCh37] Chr18:18q21.33	likely benign
NM_003784.4(SERPINB7):c.213T>A (p.Asn71Lys)	single nucleotide variant	not provided [RCV003695573]	Chr18:63792437 [GRCh38] Chr18:61459671 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.744+9C>T	single nucleotide variant	not provided [RCV003697722]	Chr18:63801021 [GRCh38] Chr18:61468255 [GRCh37] Chr18:18q21.33	likely benign
NM_003784.4(SERPINB7):c.169-8G>C	single nucleotide variant	not provided [RCV003554824]	Chr18:63792385 [GRCh38] Chr18:61459619 [GRCh37] Chr18:18q21.33	likely benign
NM_003784.4(SERPINB7):c.360A>G (p.Lys120=)	single nucleotide variant	not provided [RCV003721917]	Chr18:63796289 [GRCh38] Chr18:61463523 [GRCh37] Chr18:18q21.33	likely benign
GRCh37/hg19 18q21.31-23(chr18:55363398-78014123)x1	copy number loss	not specified [RCV003987273]	Chr18:18q21.31-23	pathogenic
NM_003784.4(SERPINB7):c.597+8G>A	single nucleotide variant	SERPINB7-related condition [RCV003943958]	Chr18:63798754 [GRCh38] Chr18:61465988 [GRCh37] Chr18:18q21.33	likely benign
NM_003784.4(SERPINB7):c.54_55del (p.Glu18fs)	microsatellite	SERPINB7-related condition [RCV003961659]	Chr18:63782421..63782422 [GRCh38] Chr18:61449655..61449656 [GRCh37] Chr18:18q21.33	likely pathogenic
NM_003784.4(SERPINB7):c.424A>G (p.Ile142Val)	single nucleotide variant	Inborn genetic diseases [RCV004665996]	Chr18:63796353 [GRCh38] Chr18:61463587 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.710T>C (p.Met237Thr)	single nucleotide variant	Inborn genetic diseases [RCV004666000]	Chr18:63800978 [GRCh38] Chr18:61468212 [GRCh37] Chr18:18q21.33	uncertain significance
GRCh37/hg19 18q11.2-23(chr18:19309942-78014123)x3	copy number gain	not provided [RCV004819319]	Chr18:18q11.2-23	pathogenic
GRCh37/hg19 18q21.33-22.1(chr18:60802235-61642539)x3	copy number gain	not provided [RCV004819640]	Chr18:18q21.33-22.1	uncertain significance
NM_003784.4(SERPINB7):c.716T>C (p.Val239Ala)	single nucleotide variant	Palmoplantar keratoderma, Nagashima type [RCV005026300]	Chr18:63800984 [GRCh38] Chr18:61468218 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.288C>G (p.Leu96=)	single nucleotide variant	not provided [RCV005174453]	Chr18:63793229 [GRCh38] Chr18:61460463 [GRCh37] Chr18:18q21.33	likely benign
NM_003784.4(SERPINB7):c.408del (p.Asp137fs)	deletion	not provided [RCV005153900]	Chr18:63796336 [GRCh38] Chr18:61463570 [GRCh37] Chr18:18q21.33	pathogenic
NM_003784.4(SERPINB7):c.336+2T>G	single nucleotide variant	not provided [RCV005203546]	Chr18:63793279 [GRCh38] Chr18:61460513 [GRCh37] Chr18:18q21.33	likely pathogenic
NM_003784.4(SERPINB7):c.759G>T (p.Leu253=)	single nucleotide variant	not provided [RCV005203772]	Chr18:63804251 [GRCh38] Chr18:61471485 [GRCh37] Chr18:18q21.33	likely benign
GRCh38/hg38 18q11.1-23(chr18:20966775-80255845)x3	copy number gain	not provided [RCV006605675]	Chr18:18q11.1-23	likely pathogenic
GRCh38/hg38 18q21.33-23(chr18:62873887-80255845)x1	copy number loss	not provided [RCV006605574]	Chr18:18q21.33-23	likely pathogenic
NM_003784.4(SERPINB7):c.1136G>T (p.Cys379Phe)	single nucleotide variant	Inborn genetic diseases [RCV005488902]	Chr18:63804628 [GRCh38] Chr18:61471862 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.305T>G (p.Leu102Arg)	single nucleotide variant	Inborn genetic diseases [RCV005488904]	Chr18:63793246 [GRCh38] Chr18:61460480 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.254C>G (p.Ser85Cys)	single nucleotide variant	Inborn genetic diseases [RCV005488895]	Chr18:63793195 [GRCh38] Chr18:61460429 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.337-109G>T	single nucleotide variant	Familial cancer of breast [RCV006128987]	Chr18:63796157 [GRCh38] Chr18:61463391 [GRCh37] Chr18:18q21.33	evidence_only
NM_003784.4(SERPINB7):c.428A>G (p.Asn143Ser)	single nucleotide variant	Inborn genetic diseases [RCV005724600]	Chr18:63796357 [GRCh38] Chr18:61463591 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.1070C>T (p.Ala357Val)	single nucleotide variant	Inborn genetic diseases [RCV005724601]	Chr18:63804562 [GRCh38] Chr18:61471796 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.281A>G (p.Tyr94Cys)	single nucleotide variant	Inborn genetic diseases [RCV005724602]	Chr18:63793222 [GRCh38] Chr18:61460456 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.553T>C (p.Phe185Leu)	single nucleotide variant	Inborn genetic diseases [RCV005724603]	Chr18:63798702 [GRCh38] Chr18:61465936 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.443dup (p.Asn148fs)	duplication	Palmoplantar keratoderma, Nagashima type [RCV006695963]	Chr18:63796368..63796369 [GRCh38] Chr18:61463602..61463603 [GRCh37] Chr18:18q21.33	likely pathogenic
NM_003784.4(SERPINB7):c.163G>A (p.Asp55Asn)	single nucleotide variant	Inborn genetic diseases [RCV005735550]	Chr18:63782535 [GRCh38] Chr18:61449769 [GRCh37] Chr18:18q21.33	uncertain significance
GRCh38/hg38 18q12.2-22.1(chr18:38794728-65632804)x3	copy number gain	See cases [RCV000136910]	Chr18:18q12.2-22.1	pathogenic
GRCh38/hg38 18p11.32-q23(chr18:118760-80254946)x3	copy number gain	Abnormal facial shape [RCV000138656]	Chr18:18p11.32-q23	pathogenic\|conflicting data from submitters
GRCh38/hg38 18q21.33-22.1(chr18:63144445-64588458)x3	copy number gain	Short stature [RCV000139938]	Chr18:18q21.33-22.1	uncertain significance
GRCh38/hg38 18q21.32-23(chr18:59996934-80254946)x1	copy number loss	Foot dorsiflexor weakness [RCV000139669]	Chr18:18q21.32-23	pathogenic
GRCh38/hg38 18q12.3-23(chr18:40367455-80256240)x3	copy number gain	Polyhydramnios [RCV000142227]	Chr18:18q12.3-23	pathogenic
GRCh38/hg38 18q21.32-22.3(chr18:59909593-72609801)x3	copy number gain	Premature birth [RCV000143195]	Chr18:18q21.32-22.3	likely pathogenic
GRCh38/hg38 18p11.32-q23(chr18:136226-80256240)x3	copy number gain	Wide intermamillary distance [RCV000143218]	Chr18:18p11.32-q23	pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80252149)x3	copy number gain	See cases [RCV000148072]	Chr18:18p11.32-q23	pathogenic
GRCh37/hg19 18p11.32-q23(chr18:1-78077248)	copy number gain	Trisomy 18 [RCV002280660]	Chr18:18p11.32-q23	pathogenic
Single allele	complex	Breast ductal adenocarcinoma [RCV000207027]	Chr18:61387312..63489378 [GRCh37] Chr18:18q21.33-22.1	uncertain significance
GRCh37/hg19 18q11.1-23(chr18:18548019-77954165)x3	copy number gain	Oligohydramnios [RCV000240476]	Chr18:18q11.1-23	pathogenic
GRCh37/hg19 18q21.33-23(chr18:59332806-78014123)x1	copy number loss	See cases [RCV000449163]	Chr18:59332806..78014123 [GRCh37] Chr18:18q21.33-23	pathogenic
GRCh37/hg19 18p11.32-q23(chr18:136226-78014123)x3	copy number gain	See cases [RCV000446047]	Chr18:136226..78014123 [GRCh37] Chr18:18p11.32-q23	pathogenic
GRCh37/hg19 18p11.32-q23(chr18:163323-78005185)x3	copy number gain	See cases [RCV000445851]	Chr18:18p11.32-q23	pathogenic
GRCh37/hg19 18q21.2-23(chr18:50224898-78014123)x1	copy number loss	Feeding difficulties [RCV000510720]	Chr18:18q21.2-23	likely pathogenic
GRCh37/hg19 18q21.1-23(chr18:47656799-78014123)x1	copy number loss	See cases [RCV000447931]	Chr18:47656799..78014123 [GRCh37] Chr18:18q21.1-23	pathogenic
GRCh37/hg19 18q12.2-23(chr18:33417216-78014123)x3	copy number gain	See cases [RCV000512081]	Chr18:18q12.2-23	pathogenic
GRCh37/hg19 18q21.1-23(chr18:47454437-78014123)x3	copy number gain	See cases [RCV000510655]	Chr18:18q21.1-23	pathogenic
GRCh37/hg19 18q21.1-23(chr18:43776770-78014123)x3	copy number gain	Disproportionate short-limb short stature [RCV000511394]	Chr18:18q21.1-23	pathogenic
GRCh37/hg19 18q12.3-23(chr18:42930373-78014123)x3	copy number gain	Delayed speech and language development [RCV000511203]	Chr18:18q12.3-23	pathogenic
GRCh37/hg19 18p11.32-q23(chr18:136227-78014123)	copy number gain	Joint hypermobility [RCV000511189]	Chr18:18p11.32-q23	pathogenic
GRCh37/hg19 18q21.33-23(chr18:59876469-78014123)x1	copy number loss	Global developmental delay [RCV000511105]	Chr18:18q21.33-23	pathogenic
NM_003784.4(SERPINB7):c.639G>T (p.Lys213Asn)	single nucleotide variant	Inborn genetic diseases [RCV003270638]	Chr18:63800907 [GRCh38] Chr18:61468141 [GRCh37] Chr18:18q21.33	uncertain significance
Single allele	deletion	Deletion of long arm of chromosome 18 [RCV000768454]	Chr18:58024137..77996821 [GRCh37] Chr18:18q21.32-23	pathogenic
GRCh37/hg19 18q12.1-23(chr18:31879854-78014123)x3	copy number gain	Ventricular septal defect [RCV000512425]	Chr18:18q12.1-23	pathogenic
GRCh37/hg19 18q21.33-23(chr18:60416709-78014123)x1	copy number loss	not provided [RCV000684055]	Chr18:18q21.33-23	pathogenic
GRCh37/hg19 18p11.32-q23(chr18:13034-78015180)x3	copy number gain	not provided [RCV000752246]	Chr18:13034..78015180 [GRCh37] Chr18:18p11.32-q23	pathogenic
GRCh37/hg19 18q21.33-23(chr18:59585959-78015180)x1	copy number loss	not provided [RCV000752366]	Chr18:59585959..78015180 [GRCh37] Chr18:18q21.33-23	pathogenic
GRCh37/hg19 18q21.33-23(chr18:60098018-78014123)x1	copy number loss	not provided [RCV001007019]	Chr18:18q21.33-23	pathogenic
GRCh37/hg19 18q21.2-23(chr18:49460596-78014123)x1	copy number loss	not provided [RCV001007016]	Chr18:18q21.2-23	pathogenic
GRCh37/hg19 18q21.33-22.1(chr18:61388176-62052163)x1	copy number loss	not provided [RCV000847942]	Chr18:18q21.33-22.1	uncertain significance
NM_003784.4(SERPINB7):c.220-325G>A	single nucleotide variant	Not Provided [RCV001713553]	Chr18:63792836 [GRCh38] Chr18:61460070 [GRCh37] Chr18:18q21.33	benign
GRCh37/hg19 18q11.2-23(chr18:23626739-78014976)x3	copy number gain	not provided [RCV001537911]	Chr18:23626739..78014976 [GRCh37] Chr18:18q11.2-23	pathogenic
GRCh37/hg19 18q21.2-23(chr18:51925586-78010032)	copy number gain	Global developmental delay [RCV001352665]	Chr18:18q21.2-23	pathogenic
GRCh37/hg19 18q21.2-23(chr18:52675201-78014123)	copy number loss	not specified [RCV002052641]	Chr18:18q21.2-23	pathogenic
GRCh37/hg19 18q21.2-22.1(chr18:50739715-63705988)	copy number loss	not specified [RCV002052639]	Chr18:18q21.2-22.1	pathogenic
GRCh37/hg19 18q21.1-23(chr18:47656799-78014123)	copy number loss	not specified [RCV002052636]	Chr18:18q21.1-23	pathogenic
NC_000018.9:g.(?_59713089)_(61654512_?)dup	duplication	Multiple congenital anomalies-hypotonia-seizures syndrome 1 [RCV002029497]	Chr18:18q21.33-22.1	uncertain significance
NM_003784.4(SERPINB7):c.337-19A>G	single nucleotide variant	not provided [RCV002146076]	Chr18:63796247 [GRCh38] Chr18:61463481 [GRCh37] Chr18:18q21.33	benign
NM_003784.4(SERPINB7):c.867A>G (p.Gln289=)	single nucleotide variant	not provided [RCV002089246]	Chr18:63804359 [GRCh38] Chr18:61471593 [GRCh37] Chr18:18q21.33	benign
NM_003784.4(SERPINB7):c.936G>T (p.Ser312=)	single nucleotide variant	not provided [RCV002123030]	Chr18:63804428 [GRCh38] Chr18:61471662 [GRCh37] Chr18:18q21.33	benign
NM_003784.4(SERPINB7):c.455-17A>T	single nucleotide variant	not provided [RCV002124224]	Chr18:63798587 [GRCh38] Chr18:61465821 [GRCh37] Chr18:18q21.33	likely benign
GRCh37/hg19 18q21.2-23(chr18:53624405-78014123)x1	copy number loss	not provided [RCV002473956]	Chr18:18q21.2-23	pathogenic
NM_003784.4(SERPINB7):c.563G>A (p.Ser188Asn)	single nucleotide variant	not provided [RCV002622678]	Chr18:63798712 [GRCh38] Chr18:61465946 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.833A>G (p.Gln278Arg)	single nucleotide variant	not provided [RCV003084823]	Chr18:63804325 [GRCh38] Chr18:61471559 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.949T>C (p.Tyr317His)	single nucleotide variant	not provided [RCV003018682]	Chr18:63804441 [GRCh38] Chr18:61471675 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.205T>C (p.Ser69Pro)	single nucleotide variant	Inborn genetic diseases [RCV002983574]	Chr18:63792429 [GRCh38] Chr18:61459663 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.121C>G (p.Leu41Val)	single nucleotide variant	Inborn genetic diseases [RCV002832174]	Chr18:63782493 [GRCh38] Chr18:61449727 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.389A>T (p.Asp130Val)	single nucleotide variant	Inborn genetic diseases [RCV002714767]	Chr18:63796318 [GRCh38] Chr18:61463552 [GRCh37] Chr18:18q21.33	uncertain significance
GRCh37/hg19 18q21.32-23(chr18:57452202-78014123)x1	copy number loss	not specified [RCV005862284]	Chr18:18q21.32-23	pathogenic
GRCh37/hg19 18q21.1-22.1(chr18:47267634-61639548)x1	copy number loss	not specified [RCV006697365]	Chr18:18q21.1-22.1	pathogenic
NM_003784.4(SERPINB7):c.-18-2A>T	single nucleotide variant	Ovarian serous cystadenocarcinoma [RCV006128985]	Chr18:63782353 [GRCh38] Chr18:61449587 [GRCh37] Chr18:18q21.33	evidence_only
GRCh37/hg19 18q21.33-22.1(chr18:60802235-61648719)x3	copy number gain	not specified [RCV005862384]	Chr18:18q21.33-22.1	uncertain significance
NM_003784.4(SERPINB7):c.344T>C (p.Ile115Thr)	single nucleotide variant	Inborn genetic diseases [RCV005488897]	Chr18:63796273 [GRCh38] Chr18:61463507 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.132G>A (p.Leu44=)	single nucleotide variant	not provided [RCV003572123]	Chr18:63782504 [GRCh38] Chr18:61449738 [GRCh37] Chr18:18q21.33	likely benign
NM_003784.4(SERPINB7):c.1045C>T (p.Leu349Phe)	single nucleotide variant	not provided [RCV003811179]	Chr18:63804537 [GRCh38] Chr18:61471771 [GRCh37] Chr18:18q21.33	uncertain significance
GRCh37/hg19 18q21.2-23(chr18:48766173-78014123)x1	copy number loss	not specified [RCV003986103]	Chr18:18q21.2-23	pathogenic
GRCh37/hg19 18q21.32-22.3(chr18:58508272-70495604)x3	copy number gain	not specified [RCV003986100]	Chr18:18q21.32-22.3	likely pathogenic
NM_003784.4(SERPINB7):c.24T>C (p.Asn8=)	single nucleotide variant	SERPINB7-related condition [RCV003922073]	Chr18:63782396 [GRCh38] Chr18:61449630 [GRCh37] Chr18:18q21.33	likely benign
NM_003784.4(SERPINB7):c.223G>A (p.Gly75Arg)	single nucleotide variant	Inborn genetic diseases [RCV004453341]	Chr18:63793164 [GRCh38] Chr18:61460398 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.1058C>T (p.Thr353Met)	single nucleotide variant	Inborn genetic diseases [RCV004453339]	Chr18:63804550 [GRCh38] Chr18:61471784 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.533A>G (p.Lys178Arg)	single nucleotide variant	Inborn genetic diseases [RCV004453343]	Chr18:63798682 [GRCh38] Chr18:61465916 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.185C>G (p.Thr62Ser)	single nucleotide variant	Inborn genetic diseases [RCV004453340]	Chr18:63792409 [GRCh38] Chr18:61459643 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.301G>A (p.Gly101Arg)	single nucleotide variant	Inborn genetic diseases [RCV004665999]	Chr18:63793242 [GRCh38] Chr18:61460476 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.621G>A (p.Met207Ile)	single nucleotide variant	Inborn genetic diseases [RCV004665997]	Chr18:63800889 [GRCh38] Chr18:61468123 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.505A>G (p.Met169Val)	single nucleotide variant	Inborn genetic diseases [RCV004970990]	Chr18:63798654 [GRCh38] Chr18:61465888 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.649T>G (p.Ser217Ala)	single nucleotide variant	Inborn genetic diseases [RCV004955029]	Chr18:63800917 [GRCh38] Chr18:61468151 [GRCh37] Chr18:18q21.33	uncertain significance
GRCh37/hg19 18q21.31-23(chr18:56102873-74360560)x3	copy number gain	not provided [RCV004819282]	Chr18:18q21.31-23	likely pathogenic
NM_003784.4(SERPINB7):c.597+18T>A	single nucleotide variant	not provided [RCV005062652]	Chr18:63798764 [GRCh38] Chr18:61465998 [GRCh37] Chr18:18q21.33	likely benign
NM_003784.4(SERPINB7):c.455G>T (p.Gly152Val)	single nucleotide variant	Not Provided [RCV005233772]	Chr18:63798604 [GRCh38] Chr18:61465838 [GRCh37] Chr18:18q21.33	pathogenic
NM_003784.4(SERPINB7):c.410A>G (p.Asp137Gly)	single nucleotide variant	Inborn genetic diseases [RCV005273465]	Chr18:63796339 [GRCh38] Chr18:61463573 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.216T>A (p.Ser72Arg)	single nucleotide variant	Inborn genetic diseases [RCV005273466]	Chr18:63792440 [GRCh38] Chr18:61459674 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.620T>C (p.Met207Thr)	single nucleotide variant	Inborn genetic diseases [RCV005273467]	Chr18:63800888 [GRCh38] Chr18:61468122 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.465G>C (p.Lys155Asn)	single nucleotide variant	Inborn genetic diseases [RCV005273462]	Chr18:63798614 [GRCh38] Chr18:61465848 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.499G>C (p.Ala167Pro)	single nucleotide variant	Inborn genetic diseases [RCV005273463]	Chr18:63798648 [GRCh38] Chr18:61465882 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.469G>A (p.Val157Met)	single nucleotide variant	Inborn genetic diseases [RCV005273464]	Chr18:63798618 [GRCh38] Chr18:61465852 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.744+1G>T	single nucleotide variant	Cervical cancer [RCV006128988]	Chr18:63801013 [GRCh38] Chr18:61468247 [GRCh37] Chr18:18q21.33	evidence_only
NM_003784.4(SERPINB7):c.917A>T (p.Asp306Val)	single nucleotide variant	Inborn genetic diseases [RCV005735547]	Chr18:63804409 [GRCh38] Chr18:61471643 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.698G>T (p.Gly233Val)	single nucleotide variant	Inborn genetic diseases [RCV005735551]	Chr18:63800966 [GRCh38] Chr18:61468200 [GRCh37] Chr18:18q21.33	uncertain significance
GRCh37/hg19 18q21.33-22.1(chr18:61195659-64583219)x1	copy number loss	not specified [RCV006697306]	Chr18:18q21.33-22.1	uncertain significance
NM_003784.4(SERPINB7):c.608A>G (p.Lys203Arg)	single nucleotide variant	Inborn genetic diseases [RCV005735548]	Chr18:63800876 [GRCh38] Chr18:61468110 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.635G>A (p.Arg212Gln)	single nucleotide variant	Inborn genetic diseases [RCV005724597]	Chr18:63800903 [GRCh38] Chr18:61468137 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.28G>A (p.Glu10Lys)	single nucleotide variant	Inborn genetic diseases [RCV005724598]	Chr18:63782400 [GRCh38] Chr18:61449634 [GRCh37] Chr18:18q21.33	uncertain significance
NM_003784.4(SERPINB7):c.54G>C (p.Glu18Asp)	single nucleotide variant	Inborn genetic diseases [RCV005735549]	Chr18:63782426 [GRCh38] Chr18:61449660 [GRCh37] Chr18:18q21.33	uncertain significance

miRNA Target Status (No longer updated)

Predicted Target Of

	Summary Value
Count of predictions:	1234
Count of miRNA genes:	402
Interacting mature miRNAs:	430
Transcripts:	ENST00000336429, ENST00000398019, ENST00000425392, ENST00000431370, ENST00000447428, ENST00000540675, ENST00000546027
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

QTLs in Region (GRCh38)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
628462165	GWAS2370394_H	asthma QTL GWAS2370394 (human)		0.000001	asthma		18	63775385	63775386	Human
628788123	GWAS2696352_H	protein measurement QTL GWAS2696352 (human)		5e-38	protein amount (VT:0010120)		18	63792182	63792183	Human
597384825	GWAS1480899_H	allergic disease QTL GWAS1480899 (human)		5e-23	allergic disease		18	63775385	63775386	Human
628554324	GWAS2462553_H	level of serpin B8 in blood QTL GWAS2462553 (human)		3e-96	level of serpin B8 in blood		18	63761390	63761391	Human
597372947	GWAS1469021_H	asthma QTL GWAS1469021 (human)		2e-08	food allergy measurement		18	63775385	63775386	Human
628426173	GWAS2334402_H	atopic asthma QTL GWAS2334402 (human)		5e-14	atopic asthma		18	63775385	63775386	Human
628785650	GWAS2693879_H	asthma QTL GWAS2693879 (human)		1e-09	asthma		18	63775385	63775386	Human
628803698	GWAS2711927_H	age of onset of childhood onset asthma QTL GWAS2711927 (human)		1e-12	age of onset of childhood onset asthma		18	63775385	63775386	Human
628436860	GWAS2345089_H	childhood onset asthma QTL GWAS2345089 (human)		1e-22	childhood onset asthma		18	63775385	63775386	Human
628554328	GWAS2462557_H	level of serpin B8 in blood QTL GWAS2462557 (human)		4e-16	level of serpin B8 in blood		18	63762376	63762377	Human
597384148	GWAS1480222_H	allergic disease, age at onset QTL GWAS1480222 (human)		6e-23	allergic disease, age at onset		18	63775385	63775386	Human
597372649	GWAS1468723_H	asthma QTL GWAS1468723 (human)		3e-09	asthma		18	63775385	63775386	Human
628496002	GWAS2404231_H	asthma QTL GWAS2404231 (human)		5e-08	asthma		18	63775385	63775386	Human
597367788	GWAS1463862_H	asthma QTL GWAS1463862 (human)		2e-09	asthma		18	63775385	63775386	Human
628462285	GWAS2370514_H	asthma, age at onset QTL GWAS2370514 (human)		7e-08	asthma, age at onset		18	63775385	63775386	Human
628444652	GWAS2352881_H	asthma QTL GWAS2352881 (human)		4e-09	asthma		18	63775385	63775386	Human
628496591	GWAS2404820_H	childhood onset asthma QTL GWAS2404820 (human)		3e-16	childhood onset asthma		18	63775385	63775386	Human
645170090	GWAS3068570_H	respiratory system disorder QTL GWAS3068570 (human)		3e-08	respiratory system disorder		18	63775385	63775386	Human
628460394	GWAS2368623_H	childhood onset asthma QTL GWAS2368623 (human)		8e-18	childhood onset asthma		18	63775385	63775386	Human

Markers in Region

RH118828

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,440,553 - 61,440,837	UniSTS	GRCh37
Build 36	18	59,591,533 - 59,591,817	RGD	NCBI36
Celera	18	58,161,070 - 58,161,354	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,141,795 - 58,142,079	UniSTS
TNG Radiation Hybrid Map	18	25341.0	UniSTS

D18S14

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,435,076 - 61,435,316	UniSTS	GRCh37
Build 36	18	59,586,056 - 59,586,296	RGD	NCBI36
Celera	18	58,155,590 - 58,155,830	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,136,309 - 58,136,549	UniSTS

ECD01447

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,444,167 - 61,445,031	UniSTS	GRCh37
Build 36	18	59,595,147 - 59,596,011	RGD	NCBI36
Celera	18	58,164,684 - 58,165,548	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,145,409 - 58,146,273	UniSTS

ECD01707

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,471,791 - 61,472,646	UniSTS	GRCh37
Build 36	18	59,622,771 - 59,623,626	RGD	NCBI36
Celera	18	58,192,249 - 58,193,104	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,173,037 - 58,173,892	UniSTS

ECD01959

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,469,930 - 61,470,776	UniSTS	GRCh37
Build 36	18	59,620,910 - 59,621,756	RGD	NCBI36
Celera	18	58,190,388 - 58,191,234	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,171,176 - 58,172,022	UniSTS

ECD02014

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,470,881 - 61,471,725	UniSTS	GRCh37
Build 36	18	59,621,861 - 59,622,705	RGD	NCBI36
Celera	18	58,191,339 - 58,192,183	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,172,127 - 58,172,971	UniSTS

ECD02580

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,419,549 - 61,420,373	UniSTS	GRCh37
Build 36	18	59,570,529 - 59,571,353	RGD	NCBI36
Celera	18	58,140,059 - 58,140,883	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,120,866 - 58,121,690	UniSTS

ECD02663

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,438,302 - 61,439,123	UniSTS	GRCh37
Build 36	18	59,589,282 - 59,590,103	RGD	NCBI36
Celera	18	58,158,819 - 58,159,640	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,139,544 - 58,140,365	UniSTS

ECD02861

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,421,249 - 61,422,063	UniSTS	GRCh37
Build 36	18	59,572,229 - 59,573,043	RGD	NCBI36
Celera	18	58,141,759 - 58,142,573	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,122,566 - 58,123,380	UniSTS

ECD03183

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,446,885 - 61,447,687	UniSTS	GRCh37
Build 36	18	59,597,865 - 59,598,667	RGD	NCBI36
Celera	18	58,167,391 - 58,168,193	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,148,115 - 58,148,917	UniSTS

ECD03474

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,463,942 - 61,464,735	UniSTS	GRCh37
Build 36	18	59,614,922 - 59,615,715	RGD	NCBI36
Celera	18	58,184,399 - 58,185,192	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,165,188 - 58,165,981	UniSTS

ECD03895

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,420,443 - 61,421,223	UniSTS	GRCh37
Build 36	18	59,571,423 - 59,572,203	RGD	NCBI36
Celera	18	58,140,953 - 58,141,733	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,121,760 - 58,122,540	UniSTS

ECD03935

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,447,708 - 61,448,487	UniSTS	GRCh37
Build 36	18	59,598,688 - 59,599,467	RGD	NCBI36
Celera	18	58,168,214 - 58,168,993	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,148,938 - 58,149,717	UniSTS

ECD04451

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,457,164 - 61,457,927	UniSTS	GRCh37
Build 36	18	59,608,144 - 59,608,907	RGD	NCBI36
Celera	18	58,177,622 - 58,178,385	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,158,412 - 58,159,175	UniSTS

ECD04790

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,440,314 - 61,441,067	UniSTS	GRCh37
Build 36	18	59,591,294 - 59,592,047	RGD	NCBI36
Celera	18	58,160,831 - 58,161,584	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,141,556 - 58,142,309	UniSTS

ECD04864

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,441,921 - 61,442,672	UniSTS	GRCh37
Build 36	18	59,592,901 - 59,593,652	RGD	NCBI36
Celera	18	58,162,438 - 58,163,189	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,143,163 - 58,143,914	UniSTS

ECD05005

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,460,058 - 61,460,805	UniSTS	GRCh37
Build 36	18	59,611,038 - 59,611,785	RGD	NCBI36
Celera	18	58,180,516 - 58,181,263	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,161,306 - 58,162,053	UniSTS

ECD05319

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,448,750 - 61,449,488	UniSTS	GRCh37
Build 36	18	59,599,730 - 59,600,468	RGD	NCBI36
Celera	18	58,169,256 - 58,169,994	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,149,980 - 58,150,718	UniSTS

ECD05846

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,439,512 - 61,440,236	UniSTS	GRCh37
Build 36	18	59,590,492 - 59,591,216	RGD	NCBI36
Celera	18	58,160,029 - 58,160,753	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,140,754 - 58,141,478	UniSTS

ECD05847

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,441,108 - 61,441,832	UniSTS	GRCh37
Build 36	18	59,592,088 - 59,592,812	RGD	NCBI36
Celera	18	58,161,625 - 58,162,349	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,142,350 - 58,143,074	UniSTS

ECD06350

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,442,686 - 61,443,396	UniSTS	GRCh37
Build 36	18	59,593,666 - 59,594,376	RGD	NCBI36
Celera	18	58,163,203 - 58,163,913	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,143,928 - 58,144,638	UniSTS

ECD07422

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,418,560 - 61,419,241	UniSTS	GRCh37
Build 36	18	59,569,540 - 59,570,221	RGD	NCBI36
Celera	18	58,139,070 - 58,139,751	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,119,877 - 58,120,558	UniSTS

ECD07533

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,430,949 - 61,431,627	UniSTS	GRCh37
Build 36	18	59,581,929 - 59,582,607	RGD	NCBI36
Celera	18	58,151,463 - 58,152,141	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,132,271 - 58,132,949	UniSTS

ECD07534

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,431,669 - 61,432,347	UniSTS	GRCh37
Build 36	18	59,582,649 - 59,583,327	RGD	NCBI36
Celera	18	58,152,183 - 58,152,861	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,132,991 - 58,133,669	UniSTS

ECD07799

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,456,436 - 61,457,107	UniSTS	GRCh37
Build 36	18	59,607,416 - 59,608,087	RGD	NCBI36
Celera	18	58,176,894 - 58,177,565	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,157,684 - 58,158,355	UniSTS

ECD08816

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,445,219 - 61,445,863	UniSTS	GRCh37
Build 36	18	59,596,199 - 59,596,843	RGD	NCBI36
Celera	18	58,165,725 - 58,166,369	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,146,449 - 58,147,093	UniSTS

ECD09031

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,446,045 - 61,446,683	UniSTS	GRCh37
Build 36	18	59,597,025 - 59,597,663	RGD	NCBI36
Celera	18	58,166,551 - 58,167,189	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,147,275 - 58,147,913	UniSTS

ECD09599

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,423,407 - 61,424,031	UniSTS	GRCh37
Build 36	18	59,574,387 - 59,575,011	RGD	NCBI36
Celera	18	58,143,915 - 58,144,539	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,124,723 - 58,125,347	UniSTS

ECD09758

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,463,167 - 61,463,787	UniSTS	GRCh37
Build 36	18	59,614,147 - 59,614,767	RGD	NCBI36
Celera	18	58,183,624 - 58,184,244	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,164,413 - 58,165,033	UniSTS

ECD10060

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,430,202 - 61,430,813	UniSTS	GRCh37
Build 36	18	59,581,182 - 59,581,793	RGD	NCBI36
Celera	18	58,150,716 - 58,151,327	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,131,524 - 58,132,135	UniSTS

ECD10477

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,466,569 - 61,467,169	UniSTS	GRCh37
Build 36	18	59,617,549 - 59,618,149	RGD	NCBI36
Celera	18	58,187,027 - 58,187,627	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,167,815 - 58,168,415	UniSTS

ECD10737

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,465,853 - 61,466,445	UniSTS	GRCh37
Build 36	18	59,616,833 - 59,617,425	RGD	NCBI36
Celera	18	58,186,311 - 58,186,903	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,167,099 - 58,167,691	UniSTS

ECD10801

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,436,931 - 61,437,521	UniSTS	GRCh37
Build 36	18	59,587,911 - 59,588,501	RGD	NCBI36
Celera	18	58,157,446 - 58,158,036	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,138,165 - 58,138,755	UniSTS

ECD11859

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,450,670 - 61,451,229	UniSTS	GRCh37
Build 36	18	59,601,650 - 59,602,209	RGD	NCBI36
Celera	18	58,171,146 - 58,171,705	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,151,870 - 58,152,429	UniSTS

ECD11860

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,452,017 - 61,452,576	UniSTS	GRCh37
Build 36	18	59,602,997 - 59,603,556	RGD	NCBI36
Celera	18	58,172,493 - 58,173,052	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,153,217 - 58,153,776	UniSTS

ECD13237

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,453,577 - 61,454,099	UniSTS	GRCh37
Build 36	18	59,604,557 - 59,605,079	RGD	NCBI36
Celera	18	58,174,036 - 58,174,557	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,154,826 - 58,155,347	UniSTS

ECD13547

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,459,147 - 61,459,661	UniSTS	GRCh37
Build 36	18	59,610,127 - 59,610,641	RGD	NCBI36
Celera	18	58,179,605 - 58,180,119	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,160,395 - 58,160,909	UniSTS

ECD15794

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,425,876 - 61,426,337	UniSTS	GRCh37
Build 36	18	59,576,856 - 59,577,317	RGD	NCBI36
Celera	18	58,146,390 - 58,146,851	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,127,198 - 58,127,659	UniSTS

ECD16140

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,425,351 - 61,425,802	UniSTS	GRCh37
Build 36	18	59,576,331 - 59,576,782	RGD	NCBI36
Celera	18	58,145,865 - 58,146,316	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,126,673 - 58,127,124	UniSTS

ECD16664

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,449,581 - 61,450,011	UniSTS	GRCh37
Build 36	18	59,600,561 - 59,600,991	RGD	NCBI36
Celera	18	58,170,087 - 58,170,517	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,150,811 - 58,151,241	UniSTS

ECD18284

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,422,441 - 61,422,806	UniSTS	GRCh37
Build 36	18	59,573,421 - 59,573,786	RGD	NCBI36
Celera	18	58,142,951 - 58,143,316	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,123,759 - 58,124,124	UniSTS

ECD18474

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,429,468 - 61,429,826	UniSTS	GRCh37
Build 36	18	59,580,448 - 59,580,806	RGD	NCBI36
Celera	18	58,149,982 - 58,150,340	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,130,790 - 58,131,148	UniSTS

ECD18475

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,433,466 - 61,433,824	UniSTS	GRCh37
Build 36	18	59,584,446 - 59,584,804	RGD	NCBI36
Celera	18	58,153,980 - 58,154,338	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,134,788 - 58,135,146	UniSTS

ECD19063

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,426,514 - 61,426,849	UniSTS	GRCh37
Build 36	18	59,577,494 - 59,577,829	RGD	NCBI36
Celera	18	58,147,028 - 58,147,363	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,127,836 - 58,128,171	UniSTS

ECD19798

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,424,970 - 61,425,278	UniSTS	GRCh37
Build 36	18	59,575,950 - 59,576,258	RGD	NCBI36
Celera	18	58,145,484 - 58,145,792	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,126,292 - 58,126,600	UniSTS

ECD19902

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,467,932 - 61,468,236	UniSTS	GRCh37
Build 36	18	59,618,912 - 59,619,216	RGD	NCBI36
Celera	18	58,188,390 - 58,188,694	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,169,178 - 58,169,482	UniSTS

ECD21269

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,458,550 - 61,458,804	UniSTS	GRCh37
Build 36	18	59,609,530 - 59,609,784	RGD	NCBI36
Celera	18	58,179,008 - 58,179,262	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,159,798 - 58,160,052	UniSTS

ECD21322

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,433,103 - 61,433,355	UniSTS	GRCh37
Build 36	18	59,584,083 - 59,584,335	RGD	NCBI36
Celera	18	58,153,617 - 58,153,869	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,134,425 - 58,134,677	UniSTS

ECD21885

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,469,393 - 61,469,628	UniSTS	GRCh37
Build 36	18	59,620,373 - 59,620,608	RGD	NCBI36
Celera	18	58,189,851 - 58,190,086	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,170,639 - 58,170,874	UniSTS

ECD22343

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,443,732 - 61,443,953	UniSTS	GRCh37
Build 36	18	59,594,712 - 59,594,933	RGD	NCBI36
Celera	18	58,164,249 - 58,164,470	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,144,974 - 58,145,195	UniSTS

ECD23041

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,451,676 - 61,451,875	UniSTS	GRCh37
Build 36	18	59,602,656 - 59,602,855	RGD	NCBI36
Celera	18	58,172,152 - 58,172,351	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,152,876 - 58,153,075	UniSTS

ECD23414

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,472,725 - 61,472,914	UniSTS	GRCh37
Build 36	18	59,623,705 - 59,623,894	RGD	NCBI36
Celera	18	58,193,183 - 58,193,372	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,173,971 - 58,174,160	UniSTS

ECD24129

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,468,481 - 61,468,639	UniSTS	GRCh37
Build 36	18	59,619,461 - 59,619,619	RGD	NCBI36
Celera	18	58,188,939 - 58,189,097	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,169,727 - 58,169,885	UniSTS

ECD24203

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,462,027 - 61,462,179	UniSTS	GRCh37
Build 36	18	59,613,007 - 59,613,159	RGD	NCBI36
Celera	18	58,182,484 - 58,182,636	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,163,272 - 58,163,424	UniSTS

REN11151

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,418,411 - 61,418,650	UniSTS	GRCh37
Build 36	18	59,569,391 - 59,569,630	RGD	NCBI36
Celera	18	58,138,921 - 58,139,160	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,119,728 - 58,119,967	UniSTS

REN11152

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,418,648 - 61,418,900	UniSTS	GRCh37
Build 36	18	59,569,628 - 59,569,880	RGD	NCBI36
Celera	18	58,139,158 - 58,139,410	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,119,965 - 58,120,217	UniSTS

REN11153

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,418,859 - 61,419,123	UniSTS	GRCh37
Build 36	18	59,569,839 - 59,570,103	RGD	NCBI36
Celera	18	58,139,369 - 58,139,633	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,120,176 - 58,120,440	UniSTS

REN11154

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,419,032 - 61,419,292	UniSTS	GRCh37
Build 36	18	59,570,012 - 59,570,272	RGD	NCBI36
Celera	18	58,139,542 - 58,139,802	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,120,349 - 58,120,609	UniSTS

REN11155

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,419,276 - 61,419,544	UniSTS	GRCh37
Build 36	18	59,570,256 - 59,570,524	RGD	NCBI36
Celera	18	58,139,786 - 58,140,054	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,120,593 - 58,120,861	UniSTS

REN11156

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,419,538 - 61,419,786	UniSTS	GRCh37
Build 36	18	59,570,518 - 59,570,766	RGD	NCBI36
Celera	18	58,140,048 - 58,140,296	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,120,855 - 58,121,103	UniSTS

REN11157

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,419,749 - 61,419,997	UniSTS	GRCh37
Build 36	18	59,570,729 - 59,570,977	RGD	NCBI36
Celera	18	58,140,259 - 58,140,507	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,121,066 - 58,121,314	UniSTS

REN11158

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,419,974 - 61,420,237	UniSTS	GRCh37
Build 36	18	59,570,954 - 59,571,217	RGD	NCBI36
Celera	18	58,140,484 - 58,140,747	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,121,291 - 58,121,554	UniSTS

REN11159

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,420,159 - 61,420,421	UniSTS	GRCh37
Build 36	18	59,571,139 - 59,571,401	RGD	NCBI36
Celera	18	58,140,669 - 58,140,931	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,121,476 - 58,121,738	UniSTS

REN11160

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,420,405 - 61,420,629	UniSTS	GRCh37
Build 36	18	59,571,385 - 59,571,609	RGD	NCBI36
Celera	18	58,140,915 - 58,141,139	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,121,722 - 58,121,946	UniSTS

REN11161

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,420,594 - 61,420,862	UniSTS	GRCh37
Build 36	18	59,571,574 - 59,571,842	RGD	NCBI36
Celera	18	58,141,104 - 58,141,372	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,121,911 - 58,122,179	UniSTS

REN11162

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,420,851 - 61,421,100	UniSTS	GRCh37
Build 36	18	59,571,831 - 59,572,080	RGD	NCBI36
Celera	18	58,141,361 - 58,141,610	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,122,168 - 58,122,417	UniSTS

REN11163

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,421,077 - 61,421,326	UniSTS	GRCh37
Build 36	18	59,572,057 - 59,572,306	RGD	NCBI36
Celera	18	58,141,587 - 58,141,836	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,122,394 - 58,122,643	UniSTS

REN11164

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,421,295 - 61,421,542	UniSTS	GRCh37
Build 36	18	59,572,275 - 59,572,522	RGD	NCBI36
Celera	18	58,141,805 - 58,142,052	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,122,612 - 58,122,859	UniSTS

REN11165

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,421,524 - 61,421,789	UniSTS	GRCh37
Build 36	18	59,572,504 - 59,572,769	RGD	NCBI36
Celera	18	58,142,034 - 58,142,299	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,122,841 - 58,123,106	UniSTS

REN11166

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,421,766 - 61,422,009	UniSTS	GRCh37
Build 36	18	59,572,746 - 59,572,989	RGD	NCBI36
Celera	18	58,142,276 - 58,142,519	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,123,083 - 58,123,326	UniSTS

REN11167

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,421,885 - 61,422,109	UniSTS	GRCh37
Build 36	18	59,572,865 - 59,573,089	RGD	NCBI36
Celera	18	58,142,395 - 58,142,619	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,123,202 - 58,123,426	UniSTS

REN11168

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,422,442 - 61,422,666	UniSTS	GRCh37
Build 36	18	59,573,422 - 59,573,646	RGD	NCBI36
Celera	18	58,142,952 - 58,143,176	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,123,760 - 58,123,984	UniSTS

REN11169

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,422,617 - 61,422,883	UniSTS	GRCh37
Build 36	18	59,573,597 - 59,573,863	RGD	NCBI36
Celera	18	58,143,127 - 58,143,393	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,123,935 - 58,124,201	UniSTS

REN11170

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,422,856 - 61,423,086	UniSTS	GRCh37
Build 36	18	59,573,836 - 59,574,066	RGD	NCBI36
Celera	18	58,143,366 - 58,143,596	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,124,174 - 58,124,404	UniSTS

REN11171

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,422,982 - 61,423,232	UniSTS	GRCh37
Build 36	18	59,573,962 - 59,574,212	RGD	NCBI36
Celera	18	58,143,492 - 58,143,742	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,124,300 - 58,124,550	UniSTS

REN11172

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,423,224 - 61,423,468	UniSTS	GRCh37
Build 36	18	59,574,204 - 59,574,448	RGD	NCBI36
Celera	18	58,143,734 - 58,143,976	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,124,542 - 58,124,784	UniSTS

REN11173

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,423,444 - 61,423,691	UniSTS	GRCh37
Build 36	18	59,574,424 - 59,574,671	RGD	NCBI36
Celera	18	58,143,952 - 58,144,199	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,124,760 - 58,125,007	UniSTS

REN11174

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,423,667 - 61,423,912	UniSTS	GRCh37
Build 36	18	59,574,647 - 59,574,892	RGD	NCBI36
Celera	18	58,144,175 - 58,144,420	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,124,983 - 58,125,228	UniSTS

REN11175

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,423,889 - 61,424,138	UniSTS	GRCh37
Build 36	18	59,574,869 - 59,575,118	RGD	NCBI36
Celera	18	58,144,397 - 58,144,652	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,125,205 - 58,125,460	UniSTS

REN11176

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,424,131 - 61,424,364	UniSTS	GRCh37
Build 36	18	59,575,111 - 59,575,344	RGD	NCBI36
Celera	18	58,144,645 - 58,144,878	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,125,453 - 58,125,686	UniSTS

REN11177

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,424,329 - 61,424,578	UniSTS	GRCh37
Build 36	18	59,575,309 - 59,575,558	RGD	NCBI36
Celera	18	58,144,843 - 58,145,092	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,125,651 - 58,125,900	UniSTS

REN11178

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,424,554 - 61,424,799	UniSTS	GRCh37
Build 36	18	59,575,534 - 59,575,779	RGD	NCBI36
Celera	18	58,145,068 - 58,145,313	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,125,876 - 58,126,121	UniSTS

REN11179

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,424,776 - 61,425,013	UniSTS	GRCh37
Build 36	18	59,575,756 - 59,575,993	RGD	NCBI36
Celera	18	58,145,290 - 58,145,527	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,126,098 - 58,126,335	UniSTS

REN11180

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,424,977 - 61,425,222	UniSTS	GRCh37
Build 36	18	59,575,957 - 59,576,202	RGD	NCBI36
Celera	18	58,145,491 - 58,145,736	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,126,299 - 58,126,544	UniSTS

REN11181

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,425,216 - 61,425,440	UniSTS	GRCh37
Build 36	18	59,576,196 - 59,576,420	RGD	NCBI36
Celera	18	58,145,730 - 58,145,954	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,126,538 - 58,126,762	UniSTS

REN11182

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,425,421 - 61,425,688	UniSTS	GRCh37
Build 36	18	59,576,401 - 59,576,668	RGD	NCBI36
Celera	18	58,145,935 - 58,146,202	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,126,743 - 58,127,010	UniSTS

REN11183

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,425,681 - 61,425,912	UniSTS	GRCh37
Build 36	18	59,576,661 - 59,576,892	RGD	NCBI36
Celera	18	58,146,195 - 58,146,426	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,127,003 - 58,127,234	UniSTS

REN11184

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,425,894 - 61,426,123	UniSTS	GRCh37
Build 36	18	59,576,874 - 59,577,103	RGD	NCBI36
Celera	18	58,146,408 - 58,146,637	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,127,216 - 58,127,445	UniSTS

REN11185

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,426,098 - 61,426,347	UniSTS	GRCh37
Build 36	18	59,577,078 - 59,577,327	RGD	NCBI36
Celera	18	58,146,612 - 58,146,861	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,127,420 - 58,127,669	UniSTS

REN11186

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,426,335 - 61,426,559	UniSTS	GRCh37
Build 36	18	59,577,315 - 59,577,539	RGD	NCBI36
Celera	18	58,146,849 - 58,147,073	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,127,657 - 58,127,881	UniSTS

REN11187

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,426,525 - 61,426,790	UniSTS	GRCh37
Build 36	18	59,577,505 - 59,577,770	RGD	NCBI36
Celera	18	58,147,039 - 58,147,304	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,127,847 - 58,128,112	UniSTS

REN11188

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,426,779 - 61,427,028	UniSTS	GRCh37
Build 36	18	59,577,759 - 59,578,008	RGD	NCBI36
Celera	18	58,147,293 - 58,147,542	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,128,101 - 58,128,350	UniSTS

REN11189

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,426,840 - 61,427,083	UniSTS	GRCh37
Build 36	18	59,577,820 - 59,578,063	RGD	NCBI36
Celera	18	58,147,354 - 58,147,597	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,128,162 - 58,128,405	UniSTS

REN11190

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,427,565 - 61,427,791	UniSTS	GRCh37
Build 36	18	59,578,545 - 59,578,771	RGD	NCBI36
Celera	18	58,148,079 - 58,148,305	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,128,887 - 58,129,113	UniSTS

REN11191

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,427,882 - 61,428,106	UniSTS	GRCh37
Build 36	18	59,578,862 - 59,579,086	RGD	NCBI36
Celera	18	58,148,396 - 58,148,620	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,129,204 - 58,129,428	UniSTS

REN11192

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,428,104 - 61,428,329	UniSTS	GRCh37
Build 36	18	59,579,084 - 59,579,309	RGD	NCBI36
Celera	18	58,148,618 - 58,148,843	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,129,426 - 58,129,651	UniSTS

REN11193

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,428,269 - 61,428,533	UniSTS	GRCh37
Build 36	18	59,579,249 - 59,579,513	RGD	NCBI36
Celera	18	58,148,783 - 58,149,047	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,129,591 - 58,129,855	UniSTS

REN11194

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,429,024 - 61,429,275	UniSTS	GRCh37
Build 36	18	59,580,004 - 59,580,255	RGD	NCBI36
Celera	18	58,149,538 - 58,149,789	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,130,346 - 58,130,597	UniSTS

REN11195

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,429,255 - 61,429,521	UniSTS	GRCh37
Build 36	18	59,580,235 - 59,580,501	RGD	NCBI36
Celera	18	58,149,769 - 58,150,035	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,130,577 - 58,130,843	UniSTS

REN11196

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,429,498 - 61,429,765	UniSTS	GRCh37
Build 36	18	59,580,478 - 59,580,745	RGD	NCBI36
Celera	18	58,150,012 - 58,150,279	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,130,820 - 58,131,087	UniSTS

REN11197

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,429,747 - 61,429,993	UniSTS	GRCh37
Build 36	18	59,580,727 - 59,580,973	RGD	NCBI36
Celera	18	58,150,261 - 58,150,507	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,131,069 - 58,131,315	UniSTS

REN11198

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,429,975 - 61,430,222	UniSTS	GRCh37
Build 36	18	59,580,955 - 59,581,202	RGD	NCBI36
Celera	18	58,150,489 - 58,150,736	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,131,297 - 58,131,544	UniSTS

REN11199

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,430,204 - 61,430,453	UniSTS	GRCh37
Build 36	18	59,581,184 - 59,581,433	RGD	NCBI36
Celera	18	58,150,718 - 58,150,967	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,131,526 - 58,131,775	UniSTS

REN11200

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,430,395 - 61,430,665	UniSTS	GRCh37
Build 36	18	59,581,375 - 59,581,645	RGD	NCBI36
Celera	18	58,150,909 - 58,151,179	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,131,717 - 58,131,987	UniSTS

REN11201

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,430,642 - 61,430,888	UniSTS	GRCh37
Build 36	18	59,581,622 - 59,581,868	RGD	NCBI36
Celera	18	58,151,156 - 58,151,402	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,131,964 - 58,132,210	UniSTS

REN11202

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,430,863 - 61,431,117	UniSTS	GRCh37
Build 36	18	59,581,843 - 59,582,097	RGD	NCBI36
Celera	18	58,151,377 - 58,151,631	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,132,185 - 58,132,439	UniSTS

REN11203

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,431,105 - 61,431,362	UniSTS	GRCh37
Build 36	18	59,582,085 - 59,582,342	RGD	NCBI36
Celera	18	58,151,619 - 58,151,876	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,132,427 - 58,132,684	UniSTS

REN11204

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,431,298 - 61,431,558	UniSTS	GRCh37
Build 36	18	59,582,278 - 59,582,538	RGD	NCBI36
Celera	18	58,151,812 - 58,152,072	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,132,620 - 58,132,880	UniSTS

REN11205

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,431,532 - 61,431,783	UniSTS	GRCh37
Build 36	18	59,582,512 - 59,582,763	RGD	NCBI36
Celera	18	58,152,046 - 58,152,297	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,132,854 - 58,133,105	UniSTS

REN11206

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,431,760 - 61,431,989	UniSTS	GRCh37
Build 36	18	59,582,740 - 59,582,969	RGD	NCBI36
Celera	18	58,152,274 - 58,152,503	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,133,082 - 58,133,311	UniSTS

REN11207

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,431,958 - 61,432,182	UniSTS	GRCh37
Build 36	18	59,582,938 - 59,583,162	RGD	NCBI36
Celera	18	58,152,472 - 58,152,696	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,133,280 - 58,133,504	UniSTS

REN11208

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,432,150 - 61,432,401	UniSTS	GRCh37
Build 36	18	59,583,130 - 59,583,381	RGD	NCBI36
Celera	18	58,152,664 - 58,152,915	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,133,472 - 58,133,723	UniSTS

REN11209

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,432,398 - 61,432,644	UniSTS	GRCh37
Build 36	18	59,583,378 - 59,583,624	RGD	NCBI36
Celera	18	58,152,912 - 58,153,158	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,133,720 - 58,133,966	UniSTS

REN11210

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,432,620 - 61,432,859	UniSTS	GRCh37
Build 36	18	59,583,600 - 59,583,839	RGD	NCBI36
Celera	18	58,153,134 - 58,153,373	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,133,942 - 58,134,181	UniSTS

REN11211

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,432,849 - 61,433,111	UniSTS	GRCh37
Build 36	18	59,583,829 - 59,584,091	RGD	NCBI36
Celera	18	58,153,363 - 58,153,625	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,134,171 - 58,134,433	UniSTS

REN11212

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,433,084 - 61,433,330	UniSTS	GRCh37
Build 36	18	59,584,064 - 59,584,310	RGD	NCBI36
Celera	18	58,153,598 - 58,153,844	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,134,406 - 58,134,652	UniSTS

REN11213

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,433,321 - 61,433,571	UniSTS	GRCh37
Build 36	18	59,584,301 - 59,584,551	RGD	NCBI36
Celera	18	58,153,835 - 58,154,085	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,134,643 - 58,134,893	UniSTS

REN11214

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,433,566 - 61,433,818	UniSTS	GRCh37
Build 36	18	59,584,546 - 59,584,798	RGD	NCBI36
Celera	18	58,154,080 - 58,154,332	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,134,888 - 58,135,140	UniSTS

REN11215

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,433,802 - 61,434,050	UniSTS	GRCh37
Build 36	18	59,584,782 - 59,585,030	RGD	NCBI36
Celera	18	58,154,316 - 58,154,564	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,135,124 - 58,135,372	UniSTS

REN11216

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,434,037 - 61,434,295	UniSTS	GRCh37
Build 36	18	59,585,017 - 59,585,275	RGD	NCBI36
Celera	18	58,154,551 - 58,154,809	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,135,359 - 58,135,617	UniSTS

REN11217

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,434,272 - 61,434,517	UniSTS	GRCh37
Build 36	18	59,585,252 - 59,585,497	RGD	NCBI36
Celera	18	58,154,786 - 58,155,031	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,135,594 - 58,135,839	UniSTS

REN11218

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,434,494 - 61,434,733	UniSTS	GRCh37
Build 36	18	59,585,474 - 59,585,713	RGD	NCBI36
Celera	18	58,155,008 - 58,155,247	RGD
Cytogenetic Map	18	q21.33	UniSTS

REN11219

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,434,727 - 61,434,968	UniSTS	GRCh37
Build 36	18	59,585,707 - 59,585,948	RGD	NCBI36
Celera	18	58,155,241 - 58,155,482	RGD
Cytogenetic Map	18	q21.33	UniSTS

REN11220

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,434,954 - 61,435,186	UniSTS	GRCh37
Build 36	18	59,585,934 - 59,586,166	RGD	NCBI36
Celera	18	58,155,468 - 58,155,700	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,136,187 - 58,136,419	UniSTS

REN11221

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,435,144 - 61,435,417	UniSTS	GRCh37
Build 36	18	59,586,124 - 59,586,397	RGD	NCBI36
Celera	18	58,155,658 - 58,155,931	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,136,377 - 58,136,650	UniSTS

REN11222

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,435,392 - 61,435,622	UniSTS	GRCh37
Build 36	18	59,586,372 - 59,586,602	RGD	NCBI36
Celera	18	58,155,906 - 58,156,136	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,136,625 - 58,136,855	UniSTS

REN11223

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,435,606 - 61,435,856	UniSTS	GRCh37
Build 36	18	59,586,586 - 59,586,836	RGD	NCBI36
Celera	18	58,156,120 - 58,156,370	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,136,839 - 58,137,089	UniSTS

REN11224

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,435,855 - 61,436,124	UniSTS	GRCh37
Build 36	18	59,586,835 - 59,587,104	RGD	NCBI36
Celera	18	58,156,369 - 58,156,638	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,137,088 - 58,137,357	UniSTS

REN11225

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,436,112 - 61,436,356	UniSTS	GRCh37
Build 36	18	59,587,092 - 59,587,336	RGD	NCBI36
Celera	18	58,156,626 - 58,156,870	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,137,345 - 58,137,589	UniSTS

REN11226

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,436,304 - 61,436,528	UniSTS	GRCh37
Build 36	18	59,587,284 - 59,587,508	RGD	NCBI36
Celera	18	58,156,818 - 58,157,043	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,137,537 - 58,137,762	UniSTS

REN11227

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,436,499 - 61,436,725	UniSTS	GRCh37
Build 36	18	59,587,479 - 59,587,705	RGD	NCBI36
Celera	18	58,157,014 - 58,157,240	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,137,733 - 58,137,959	UniSTS

REN11228

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,436,714 - 61,436,959	UniSTS	GRCh37
Build 36	18	59,587,694 - 59,587,939	RGD	NCBI36
Celera	18	58,157,229 - 58,157,474	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,137,948 - 58,138,193	UniSTS

REN11229

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,436,933 - 61,437,176	UniSTS	GRCh37
Build 36	18	59,587,913 - 59,588,156	RGD	NCBI36
Celera	18	58,157,448 - 58,157,691	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,138,167 - 58,138,410	UniSTS

REN11230

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,437,153 - 61,437,405	UniSTS	GRCh37
Build 36	18	59,588,133 - 59,588,385	RGD	NCBI36
Celera	18	58,157,668 - 58,157,920	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,138,387 - 58,138,639	UniSTS

REN11231

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,437,382 - 61,437,621	UniSTS	GRCh37
Build 36	18	59,588,362 - 59,588,601	RGD	NCBI36
Celera	18	58,157,897 - 58,158,136	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,138,616 - 58,138,855	UniSTS

REN11232

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,437,603 - 61,437,844	UniSTS	GRCh37
Build 36	18	59,588,583 - 59,588,824	RGD	NCBI36
Celera	18	58,158,118 - 58,158,359	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,138,837 - 58,139,078	UniSTS

REN11233

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,437,843 - 61,438,108	UniSTS	GRCh37
Build 36	18	59,588,823 - 59,589,088	RGD	NCBI36
Celera	18	58,158,358 - 58,158,623	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,139,077 - 58,139,342	UniSTS

REN11234

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,438,076 - 61,438,323	UniSTS	GRCh37
Build 36	18	59,589,056 - 59,589,303	RGD	NCBI36
Celera	18	58,158,591 - 58,158,840	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,139,310 - 58,139,565	UniSTS

REN11235

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,438,309 - 61,438,555	UniSTS	GRCh37
Build 36	18	59,589,289 - 59,589,535	RGD	NCBI36
Celera	18	58,158,826 - 58,159,072	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,139,551 - 58,139,797	UniSTS

REN11236

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,438,550 - 61,438,794	UniSTS	GRCh37
Build 36	18	59,589,530 - 59,589,774	RGD	NCBI36
Celera	18	58,159,067 - 58,159,311	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,139,792 - 58,140,036	UniSTS

REN11237

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,438,730 - 61,438,984	UniSTS	GRCh37
Build 36	18	59,589,710 - 59,589,964	RGD	NCBI36
Celera	18	58,159,247 - 58,159,501	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,139,972 - 58,140,226	UniSTS

REN11238

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,438,957 - 61,439,198	UniSTS	GRCh37
Build 36	18	59,589,937 - 59,590,178	RGD	NCBI36
Celera	18	58,159,474 - 58,159,715	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,140,199 - 58,140,440	UniSTS

REN11239

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,439,174 - 61,439,398	UniSTS	GRCh37
Build 36	18	59,590,154 - 59,590,378	RGD	NCBI36
Celera	18	58,159,691 - 58,159,915	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,140,416 - 58,140,640	UniSTS

REN11240

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,439,373 - 61,439,623	UniSTS	GRCh37
Build 36	18	59,590,353 - 59,590,603	RGD	NCBI36
Celera	18	58,159,890 - 58,160,140	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,140,615 - 58,140,865	UniSTS

REN11241

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,439,606 - 61,439,846	UniSTS	GRCh37
Build 36	18	59,590,586 - 59,590,826	RGD	NCBI36
Celera	18	58,160,123 - 58,160,363	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,140,848 - 58,141,088	UniSTS

REN11242

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,439,823 - 61,440,071	UniSTS	GRCh37
Build 36	18	59,590,803 - 59,591,051	RGD	NCBI36
Celera	18	58,160,340 - 58,160,588	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,141,065 - 58,141,313	UniSTS

REN11243

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,440,048 - 61,440,316	UniSTS	GRCh37
Build 36	18	59,591,028 - 59,591,296	RGD	NCBI36
Celera	18	58,160,565 - 58,160,833	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,141,290 - 58,141,558	UniSTS

REN11244

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,440,315 - 61,440,581	UniSTS	GRCh37
Build 36	18	59,591,295 - 59,591,561	RGD	NCBI36
Celera	18	58,160,832 - 58,161,098	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,141,557 - 58,141,823	UniSTS

REN11245

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,440,558 - 61,440,800	UniSTS	GRCh37
Build 36	18	59,591,538 - 59,591,780	RGD	NCBI36
Celera	18	58,161,075 - 58,161,317	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,141,800 - 58,142,042	UniSTS

REN11246

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,440,777 - 61,441,032	UniSTS	GRCh37
Build 36	18	59,591,757 - 59,592,012	RGD	NCBI36
Celera	18	58,161,294 - 58,161,549	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,142,019 - 58,142,274	UniSTS

REN11247

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,441,009 - 61,441,269	UniSTS	GRCh37
Build 36	18	59,591,989 - 59,592,249	RGD	NCBI36
Celera	18	58,161,526 - 58,161,786	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,142,251 - 58,142,511	UniSTS

REN11248

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,441,264 - 61,441,503	UniSTS	GRCh37
Build 36	18	59,592,244 - 59,592,483	RGD	NCBI36
Celera	18	58,161,781 - 58,162,020	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,142,506 - 58,142,745	UniSTS

REN11249

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,441,475 - 61,441,716	UniSTS	GRCh37
Build 36	18	59,592,455 - 59,592,696	RGD	NCBI36
Celera	18	58,161,992 - 58,162,233	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,142,717 - 58,142,958	UniSTS

REN11250

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,441,694 - 61,441,943	UniSTS	GRCh37
Build 36	18	59,592,674 - 59,592,923	RGD	NCBI36
Celera	18	58,162,211 - 58,162,460	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,142,936 - 58,143,185	UniSTS

REN11251

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,441,924 - 61,442,164	UniSTS	GRCh37
Build 36	18	59,592,904 - 59,593,144	RGD	NCBI36
Celera	18	58,162,441 - 58,162,681	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,143,166 - 58,143,406	UniSTS

REN11252

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,442,134 - 61,442,402	UniSTS	GRCh37
Build 36	18	59,593,114 - 59,593,382	RGD	NCBI36
Celera	18	58,162,651 - 58,162,919	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,143,376 - 58,143,644	UniSTS

REN11253

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,442,396 - 61,442,657	UniSTS	GRCh37
Build 36	18	59,593,376 - 59,593,637	RGD	NCBI36
Celera	18	58,162,913 - 58,163,174	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,143,638 - 58,143,899	UniSTS

REN11254

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,442,634 - 61,442,885	UniSTS	GRCh37
Build 36	18	59,593,614 - 59,593,865	RGD	NCBI36
Celera	18	58,163,151 - 58,163,402	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,143,876 - 58,144,127	UniSTS

REN11255

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,442,874 - 61,443,098	UniSTS	GRCh37
Build 36	18	59,593,854 - 59,594,078	RGD	NCBI36
Celera	18	58,163,391 - 58,163,615	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,144,116 - 58,144,340	UniSTS

REN11256

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,443,074 - 61,443,323	UniSTS	GRCh37
Build 36	18	59,594,054 - 59,594,303	RGD	NCBI36
Celera	18	58,163,591 - 58,163,840	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,144,316 - 58,144,565	UniSTS

REN11257

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,443,309 - 61,443,547	UniSTS	GRCh37
Build 36	18	59,594,289 - 59,594,527	RGD	NCBI36
Celera	18	58,163,826 - 58,164,064	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,144,551 - 58,144,789	UniSTS

REN11258

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,443,523 - 61,443,761	UniSTS	GRCh37
Build 36	18	59,594,503 - 59,594,741	RGD	NCBI36
Celera	18	58,164,040 - 58,164,278	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,144,765 - 58,145,003	UniSTS

REN11259

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,443,722 - 61,443,950	UniSTS	GRCh37
Build 36	18	59,594,702 - 59,594,930	RGD	NCBI36
Celera	18	58,164,239 - 58,164,467	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,144,964 - 58,145,192	UniSTS

REN11260

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,443,928 - 61,444,188	UniSTS	GRCh37
Build 36	18	59,594,908 - 59,595,168	RGD	NCBI36
Celera	18	58,164,445 - 58,164,705	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,145,170 - 58,145,430	UniSTS

REN11261

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,444,165 - 61,444,395	UniSTS	GRCh37
Build 36	18	59,595,145 - 59,595,375	RGD	NCBI36
Celera	18	58,164,682 - 58,164,912	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,145,407 - 58,145,637	UniSTS

REN11262

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,444,378 - 61,444,620	UniSTS	GRCh37
Build 36	18	59,595,358 - 59,595,600	RGD	NCBI36
Celera	18	58,164,895 - 58,165,137	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,145,620 - 58,145,862	UniSTS

REN11263

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,444,516 - 61,444,740	UniSTS	GRCh37
Build 36	18	59,595,496 - 59,595,720	RGD	NCBI36
Celera	18	58,165,033 - 58,165,257	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,145,758 - 58,145,982	UniSTS

REN11264

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,444,695 - 61,444,946	UniSTS	GRCh37
Build 36	18	59,595,675 - 59,595,926	RGD	NCBI36
Celera	18	58,165,212 - 58,165,463	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,145,937 - 58,146,188	UniSTS

REN11265

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,444,969 - 61,445,207	UniSTS	GRCh37
Build 36	18	59,595,949 - 59,596,187	RGD	NCBI36
Celera	18	58,165,486 - 58,165,713	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,146,211 - 58,146,437	UniSTS

REN11266

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,445,165 - 61,445,425	UniSTS	GRCh37
Build 36	18	59,596,145 - 59,596,405	RGD	NCBI36
Celera	18	58,165,671 - 58,165,931	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,146,395 - 58,146,655	UniSTS

REN11267

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,445,409 - 61,445,645	UniSTS	GRCh37
Build 36	18	59,596,389 - 59,596,625	RGD	NCBI36
Celera	18	58,165,915 - 58,166,151	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,146,639 - 58,146,875	UniSTS

REN11268

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,445,615 - 61,445,871	UniSTS	GRCh37
Build 36	18	59,596,595 - 59,596,851	RGD	NCBI36
Celera	18	58,166,121 - 58,166,377	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,146,845 - 58,147,101	UniSTS

REN11269

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,445,855 - 61,446,120	UniSTS	GRCh37
Build 36	18	59,596,835 - 59,597,100	RGD	NCBI36
Celera	18	58,166,361 - 58,166,626	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,147,085 - 58,147,350	UniSTS

REN11270

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,446,097 - 61,446,349	UniSTS	GRCh37
Build 36	18	59,597,077 - 59,597,329	RGD	NCBI36
Celera	18	58,166,603 - 58,166,855	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,147,327 - 58,147,579	UniSTS

REN11271

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,446,334 - 61,446,559	UniSTS	GRCh37
Build 36	18	59,597,314 - 59,597,539	RGD	NCBI36
Celera	18	58,166,840 - 58,167,065	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,147,564 - 58,147,789	UniSTS

REN11272

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,446,464 - 61,446,688	UniSTS	GRCh37
Build 36	18	59,597,444 - 59,597,668	RGD	NCBI36
Celera	18	58,166,970 - 58,167,194	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,147,694 - 58,147,918	UniSTS

REN11273

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,446,662 - 61,446,908	UniSTS	GRCh37
Build 36	18	59,597,642 - 59,597,888	RGD	NCBI36
Celera	18	58,167,168 - 58,167,414	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,147,892 - 58,148,138	UniSTS

REN11274

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,446,884 - 61,447,149	UniSTS	GRCh37
Build 36	18	59,597,864 - 59,598,129	RGD	NCBI36
Celera	18	58,167,390 - 58,167,655	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,148,114 - 58,148,379	UniSTS

REN11275

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,447,144 - 61,447,410	UniSTS	GRCh37
Build 36	18	59,598,124 - 59,598,390	RGD	NCBI36
Celera	18	58,167,650 - 58,167,916	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,148,374 - 58,148,640	UniSTS

REN11276

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,447,301 - 61,447,525	UniSTS	GRCh37
Build 36	18	59,598,281 - 59,598,505	RGD	NCBI36
Celera	18	58,167,807 - 58,168,031	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,148,531 - 58,148,755	UniSTS

REN11277

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,447,495 - 61,447,751	UniSTS	GRCh37
Build 36	18	59,598,475 - 59,598,731	RGD	NCBI36
Celera	18	58,168,001 - 58,168,257	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,148,725 - 58,148,981	UniSTS

REN11278

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,447,728 - 61,447,966	UniSTS	GRCh37
Build 36	18	59,598,708 - 59,598,946	RGD	NCBI36
Celera	18	58,168,234 - 58,168,472	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,148,958 - 58,149,196	UniSTS

REN11279

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,447,957 - 61,448,221	UniSTS	GRCh37
Build 36	18	59,598,937 - 59,599,201	RGD	NCBI36
Celera	18	58,168,463 - 58,168,727	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,149,187 - 58,149,451	UniSTS

REN11280

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,448,196 - 61,448,468	UniSTS	GRCh37
Build 36	18	59,599,176 - 59,599,448	RGD	NCBI36
Celera	18	58,168,702 - 58,168,974	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,149,426 - 58,149,698	UniSTS

REN11281

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,448,453 - 61,448,698	UniSTS	GRCh37
Build 36	18	59,599,433 - 59,599,678	RGD	NCBI36
Celera	18	58,168,959 - 58,169,204	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,149,683 - 58,149,928	UniSTS

REN11282

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,448,676 - 61,448,921	UniSTS	GRCh37
Build 36	18	59,599,656 - 59,599,901	RGD	NCBI36
Celera	18	58,169,182 - 58,169,427	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,149,906 - 58,150,151	UniSTS

REN11283

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,448,917 - 61,449,150	UniSTS	GRCh37
Build 36	18	59,599,897 - 59,600,130	RGD	NCBI36
Celera	18	58,169,423 - 58,169,656	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,150,147 - 58,150,380	UniSTS

REN11284

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,449,127 - 61,449,398	UniSTS	GRCh37
Build 36	18	59,600,107 - 59,600,378	RGD	NCBI36
Celera	18	58,169,633 - 58,169,904	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,150,357 - 58,150,628	UniSTS

REN11285

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,449,375 - 61,449,648	UniSTS	GRCh37
Build 36	18	59,600,355 - 59,600,628	RGD	NCBI36
Celera	18	58,169,881 - 58,170,154	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,150,605 - 58,150,878	UniSTS

REN11286

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,449,634 - 61,449,874	UniSTS	GRCh37
Build 36	18	59,600,614 - 59,600,854	RGD	NCBI36
Celera	18	58,170,140 - 58,170,380	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,150,864 - 58,151,104	UniSTS

REN11287

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,449,863 - 61,450,088	UniSTS	GRCh37
Build 36	18	59,600,843 - 59,601,068	RGD	NCBI36
Celera	18	58,170,369 - 58,170,594	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,151,093 - 58,151,318	UniSTS

REN11288

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,450,321 - 61,450,587	UniSTS	GRCh37
Build 36	18	59,601,301 - 59,601,567	RGD	NCBI36
Celera	18	58,170,827 - 58,171,063	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,151,551 - 58,151,787	UniSTS

REN11289

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,450,563 - 61,450,795	UniSTS	GRCh37
Build 36	18	59,601,543 - 59,601,775	RGD	NCBI36
Celera	18	58,171,039 - 58,171,271	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,151,763 - 58,151,995	UniSTS

REN11290

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,450,778 - 61,451,027	UniSTS	GRCh37
Build 36	18	59,601,758 - 59,602,007	RGD	NCBI36
Celera	18	58,171,254 - 58,171,503	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,151,978 - 58,152,227	UniSTS

REN11291

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,451,014 - 61,451,250	UniSTS	GRCh37
Build 36	18	59,601,994 - 59,602,230	RGD	NCBI36
Celera	18	58,171,490 - 58,171,726	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,152,214 - 58,152,450	UniSTS

REN11292

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,451,220 - 61,451,486	UniSTS	GRCh37
Build 36	18	59,602,200 - 59,602,466	RGD	NCBI36
Celera	18	58,171,696 - 58,171,962	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,152,420 - 58,152,686	UniSTS

REN11293

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,451,457 - 61,451,697	UniSTS	GRCh37
Build 36	18	59,602,437 - 59,602,677	RGD	NCBI36
Celera	18	58,171,933 - 58,172,173	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,152,657 - 58,152,897	UniSTS

REN11294

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,451,674 - 61,451,926	UniSTS	GRCh37
Build 36	18	59,602,654 - 59,602,906	RGD	NCBI36
Celera	18	58,172,150 - 58,172,402	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,152,874 - 58,153,126	UniSTS

REN11295

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,451,912 - 61,452,157	UniSTS	GRCh37
Build 36	18	59,602,892 - 59,603,137	RGD	NCBI36
Celera	18	58,172,388 - 58,172,633	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,153,112 - 58,153,357	UniSTS

REN11296

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,452,154 - 61,452,393	UniSTS	GRCh37
Build 36	18	59,603,134 - 59,603,373	RGD	NCBI36
Celera	18	58,172,630 - 58,172,869	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,153,354 - 58,153,593	UniSTS

REN11297

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,452,369 - 61,452,617	UniSTS	GRCh37
Build 36	18	59,603,349 - 59,603,597	RGD	NCBI36
Celera	18	58,172,845 - 58,173,093	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,153,569 - 58,153,817	UniSTS

REN11298

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,452,602 - 61,452,850	UniSTS	GRCh37
Build 36	18	59,603,582 - 59,603,830	RGD	NCBI36
Celera	18	58,173,078 - 58,173,326	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,153,802 - 58,154,050	UniSTS

REN11299

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,452,827 - 61,453,095	UniSTS	GRCh37
Build 36	18	59,603,807 - 59,604,075	RGD	NCBI36
Celera	18	58,173,303 - 58,173,571	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,154,027 - 58,154,295	UniSTS

REN11300

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,452,886 - 61,453,110	UniSTS	GRCh37
Build 36	18	59,603,866 - 59,604,090	RGD	NCBI36
Celera	18	58,173,362 - 58,173,586	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,154,086 - 58,154,310	UniSTS

REN11301

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,453,558 - 61,453,789	UniSTS	GRCh37
Build 36	18	59,604,538 - 59,604,769	RGD	NCBI36
Celera	18	58,174,017 - 58,174,248	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,154,807 - 58,155,038	UniSTS

REN11302

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,453,763 - 61,454,009	UniSTS	GRCh37
Build 36	18	59,604,743 - 59,604,989	RGD	NCBI36
Celera	18	58,174,222 - 58,174,467	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,155,012 - 58,155,257	UniSTS

REN11303

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,454,000 - 61,454,262	UniSTS	GRCh37
Build 36	18	59,604,980 - 59,605,242	RGD	NCBI36
Celera	18	58,174,458 - 58,174,720	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,155,248 - 58,155,510	UniSTS

REN11304

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,454,245 - 61,454,494	UniSTS	GRCh37
Build 36	18	59,605,225 - 59,605,474	RGD	NCBI36
Celera	18	58,174,703 - 58,174,952	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,155,493 - 58,155,742	UniSTS

REN11305

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,454,472 - 61,454,734	UniSTS	GRCh37
Build 36	18	59,605,452 - 59,605,714	RGD	NCBI36
Celera	18	58,174,930 - 58,175,192	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,155,720 - 58,155,982	UniSTS

REN11306

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,454,709 - 61,454,945	UniSTS	GRCh37
Build 36	18	59,605,689 - 59,605,925	RGD	NCBI36
Celera	18	58,175,167 - 58,175,403	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,155,957 - 58,156,193	UniSTS

REN11307

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,454,920 - 61,455,164	UniSTS	GRCh37
Build 36	18	59,605,900 - 59,606,144	RGD	NCBI36
Celera	18	58,175,378 - 58,175,622	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,156,168 - 58,156,412	UniSTS

REN11308

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,455,157 - 61,455,419	UniSTS	GRCh37
Build 36	18	59,606,137 - 59,606,399	RGD	NCBI36
Celera	18	58,175,615 - 58,175,877	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,156,405 - 58,156,667	UniSTS

REN11309

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,455,415 - 61,455,678	UniSTS	GRCh37
Build 36	18	59,606,395 - 59,606,658	RGD	NCBI36
Celera	18	58,175,873 - 58,176,136	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,156,663 - 58,156,926	UniSTS

REN11310

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,455,666 - 61,455,895	UniSTS	GRCh37
Build 36	18	59,606,646 - 59,606,875	RGD	NCBI36
Celera	18	58,176,124 - 58,176,353	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,156,914 - 58,157,143	UniSTS

REN11311

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,455,866 - 61,456,107	UniSTS	GRCh37
Build 36	18	59,606,846 - 59,607,087	RGD	NCBI36
Celera	18	58,176,324 - 58,176,565	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,157,114 - 58,157,355	UniSTS

REN11312

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,456,070 - 61,456,294	UniSTS	GRCh37
Build 36	18	59,607,050 - 59,607,274	RGD	NCBI36
Celera	18	58,176,528 - 58,176,752	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,157,318 - 58,157,542	UniSTS

REN11313

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,456,262 - 61,456,502	UniSTS	GRCh37
Build 36	18	59,607,242 - 59,607,482	RGD	NCBI36
Celera	18	58,176,720 - 58,176,960	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,157,510 - 58,157,750	UniSTS

REN11314

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,456,479 - 61,456,724	UniSTS	GRCh37
Build 36	18	59,607,459 - 59,607,704	RGD	NCBI36
Celera	18	58,176,937 - 58,177,182	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,157,727 - 58,157,972	UniSTS

REN11315

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,456,700 - 61,456,933	UniSTS	GRCh37
Build 36	18	59,607,680 - 59,607,913	RGD	NCBI36
Celera	18	58,177,158 - 58,177,391	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,157,948 - 58,158,181	UniSTS

REN11316

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,456,926 - 61,457,167	UniSTS	GRCh37
Build 36	18	59,607,906 - 59,608,147	RGD	NCBI36
Celera	18	58,177,384 - 58,177,625	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,158,174 - 58,158,415	UniSTS

REN11317

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,457,164 - 61,457,388	UniSTS	GRCh37
Build 36	18	59,608,144 - 59,608,368	RGD	NCBI36
Celera	18	58,177,622 - 58,177,846	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,158,412 - 58,158,636	UniSTS

REN11318

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,457,360 - 61,457,605	UniSTS	GRCh37
Build 36	18	59,608,340 - 59,608,585	RGD	NCBI36
Celera	18	58,177,818 - 58,178,063	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,158,608 - 58,158,853	UniSTS

REN11319

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,457,594 - 61,457,818	UniSTS	GRCh37
Build 36	18	59,608,574 - 59,608,798	RGD	NCBI36
Celera	18	58,178,052 - 58,178,276	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,158,842 - 58,159,066	UniSTS

REN11320

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,457,788 - 61,458,012	UniSTS	GRCh37
Build 36	18	59,608,768 - 59,608,992	RGD	NCBI36
Celera	18	58,178,246 - 58,178,470	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,159,036 - 58,159,260	UniSTS

REN11321

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,458,335 - 61,458,575	UniSTS	GRCh37
Build 36	18	59,609,315 - 59,609,555	RGD	NCBI36
Celera	18	58,178,793 - 58,179,033	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,159,583 - 58,159,823	UniSTS

REN11322

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,458,548 - 61,458,807	UniSTS	GRCh37
Build 36	18	59,609,528 - 59,609,787	RGD	NCBI36
Celera	18	58,179,006 - 58,179,265	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,159,796 - 58,160,055	UniSTS

REN11323

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,458,614 - 61,458,839	UniSTS	GRCh37
Build 36	18	59,609,594 - 59,609,819	RGD	NCBI36
Celera	18	58,179,072 - 58,179,297	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,159,862 - 58,160,087	UniSTS

REN11324

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,459,141 - 61,459,368	UniSTS	GRCh37
Build 36	18	59,610,121 - 59,610,348	RGD	NCBI36
Celera	18	58,179,599 - 58,179,826	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,160,389 - 58,160,616	UniSTS

REN11325

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,459,357 - 61,459,615	UniSTS	GRCh37
Build 36	18	59,610,337 - 59,610,595	RGD	NCBI36
Celera	18	58,179,815 - 58,180,073	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,160,605 - 58,160,863	UniSTS

REN11326

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,459,475 - 61,459,723	UniSTS	GRCh37
Build 36	18	59,610,455 - 59,610,703	RGD	NCBI36
Celera	18	58,179,933 - 58,180,181	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,160,723 - 58,160,971	UniSTS

REN11327

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,459,702 - 61,459,932	UniSTS	GRCh37
Build 36	18	59,610,682 - 59,610,912	RGD	NCBI36
Celera	18	58,180,160 - 58,180,390	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,160,950 - 58,161,180	UniSTS

REN11328

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,459,917 - 61,460,176	UniSTS	GRCh37
Build 36	18	59,610,897 - 59,611,156	RGD	NCBI36
Celera	18	58,180,375 - 58,180,634	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,161,165 - 58,161,424	UniSTS

REN11329

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,460,146 - 61,460,410	UniSTS	GRCh37
Build 36	18	59,611,126 - 59,611,390	RGD	NCBI36
Celera	18	58,180,604 - 58,180,868	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,161,394 - 58,161,658	UniSTS

REN11330

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,460,387 - 61,460,624	UniSTS	GRCh37
Build 36	18	59,611,367 - 59,611,604	RGD	NCBI36
Celera	18	58,180,845 - 58,181,082	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,161,635 - 58,161,872	UniSTS

REN11331

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,460,600 - 61,460,846	UniSTS	GRCh37
Build 36	18	59,611,580 - 59,611,826	RGD	NCBI36
Celera	18	58,181,058 - 58,181,304	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,161,848 - 58,162,094	UniSTS

REN11332

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,460,834 - 61,461,105	UniSTS	GRCh37
Build 36	18	59,611,814 - 59,612,085	RGD	NCBI36
Celera	18	58,181,292 - 58,181,563	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,162,082 - 58,162,353	UniSTS

REN11333

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,460,963 - 61,461,225	UniSTS	GRCh37
Build 36	18	59,611,943 - 59,612,205	RGD	NCBI36
Celera	18	58,181,421 - 58,181,683	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,162,211 - 58,162,473	UniSTS

REN11334

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,461,372 - 61,461,597	UniSTS	GRCh37
Build 36	18	59,612,352 - 59,612,577	RGD	NCBI36
Celera	18	58,181,830 - 58,182,055	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,162,618 - 58,162,843	UniSTS

REN11335

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,461,377 - 61,461,615	UniSTS	GRCh37
Build 36	18	59,612,357 - 59,612,595	RGD	NCBI36
Celera	18	58,181,835 - 58,182,073	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,162,623 - 58,162,861	UniSTS

REN11336

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,461,964 - 61,462,188	UniSTS	GRCh37
Build 36	18	59,612,944 - 59,613,168	RGD	NCBI36
Celera	18	58,182,421 - 58,182,645	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,163,209 - 58,163,433	UniSTS

REN11337

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,462,155 - 61,462,423	UniSTS	GRCh37
Build 36	18	59,613,135 - 59,613,403	RGD	NCBI36
Celera	18	58,182,612 - 58,182,880	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,163,400 - 58,163,668	UniSTS

REN11338

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,462,291 - 61,462,518	UniSTS	GRCh37
Build 36	18	59,613,271 - 59,613,498	RGD	NCBI36
Celera	18	58,182,748 - 58,182,975	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,163,536 - 58,163,763	UniSTS

REN11339

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,462,771 - 61,463,016	UniSTS	GRCh37
Build 36	18	59,613,751 - 59,613,996	RGD	NCBI36
Celera	18	58,183,228 - 58,183,473	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,164,016 - 58,164,262	UniSTS

REN11340

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,463,007 - 61,463,246	UniSTS	GRCh37
Build 36	18	59,613,987 - 59,614,226	RGD	NCBI36
Celera	18	58,183,464 - 58,183,703	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,164,253 - 58,164,492	UniSTS

REN11341

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,463,229 - 61,463,481	UniSTS	GRCh37
Build 36	18	59,614,209 - 59,614,461	RGD	NCBI36
Celera	18	58,183,686 - 58,183,938	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,164,475 - 58,164,727	UniSTS

REN11342

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,463,456 - 61,463,697	UniSTS	GRCh37
Build 36	18	59,614,436 - 59,614,677	RGD	NCBI36
Celera	18	58,183,913 - 58,184,154	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,164,702 - 58,164,943	UniSTS

REN11343

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,463,664 - 61,463,891	UniSTS	GRCh37
Build 36	18	59,614,644 - 59,614,871	RGD	NCBI36
Celera	18	58,184,121 - 58,184,348	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,164,910 - 58,165,137	UniSTS

REN11344

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,463,859 - 61,464,120	UniSTS	GRCh37
Build 36	18	59,614,839 - 59,615,100	RGD	NCBI36
Celera	18	58,184,316 - 58,184,577	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,165,105 - 58,165,366	UniSTS

REN11345

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,464,090 - 61,464,334	UniSTS	GRCh37
Build 36	18	59,615,070 - 59,615,314	RGD	NCBI36
Celera	18	58,184,547 - 58,184,791	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,165,336 - 58,165,580	UniSTS

REN11346

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,464,311 - 61,464,538	UniSTS	GRCh37
Build 36	18	59,615,291 - 59,615,518	RGD	NCBI36
Celera	18	58,184,768 - 58,184,995	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,165,557 - 58,165,784	UniSTS

REN11347

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,464,529 - 61,464,791	UniSTS	GRCh37
Build 36	18	59,615,509 - 59,615,771	RGD	NCBI36
Celera	18	58,184,986 - 58,185,248	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,165,775 - 58,166,037	UniSTS

REN11348

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,464,763 - 61,465,003	UniSTS	GRCh37
Build 36	18	59,615,743 - 59,615,983	RGD	NCBI36
Celera	18	58,185,220 - 58,185,460	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,166,009 - 58,166,249	UniSTS

REN11349

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,464,988 - 61,465,241	UniSTS	GRCh37
Build 36	18	59,615,968 - 59,616,221	RGD	NCBI36
Celera	18	58,185,445 - 58,185,698	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,166,234 - 58,166,487	UniSTS

REN11350

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,465,210 - 61,465,475	UniSTS	GRCh37
Build 36	18	59,616,190 - 59,616,455	RGD	NCBI36
Celera	18	58,185,667 - 58,185,932	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,166,456 - 58,166,721	UniSTS

REN11351

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,465,452 - 61,465,700	UniSTS	GRCh37
Build 36	18	59,616,432 - 59,616,680	RGD	NCBI36
Celera	18	58,185,909 - 58,186,157	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,166,698 - 58,166,946	UniSTS

REN11352

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,465,682 - 61,465,923	UniSTS	GRCh37
Build 36	18	59,616,662 - 59,616,903	RGD	NCBI36
Celera	18	58,186,139 - 58,186,381	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,166,928 - 58,167,169	UniSTS

REN11353

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,465,900 - 61,466,162	UniSTS	GRCh37
Build 36	18	59,616,880 - 59,617,142	RGD	NCBI36
Celera	18	58,186,358 - 58,186,620	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,167,146 - 58,167,408	UniSTS

REN11354

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,466,152 - 61,466,393	UniSTS	GRCh37
Build 36	18	59,617,132 - 59,617,373	RGD	NCBI36
Celera	18	58,186,610 - 58,186,851	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,167,398 - 58,167,639	UniSTS

REN11355

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,466,387 - 61,466,643	UniSTS	GRCh37
Build 36	18	59,617,367 - 59,617,623	RGD	NCBI36
Celera	18	58,186,845 - 58,187,101	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,167,633 - 58,167,889	UniSTS

REN11356

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,466,618 - 61,466,862	UniSTS	GRCh37
Build 36	18	59,617,598 - 59,617,842	RGD	NCBI36
Celera	18	58,187,076 - 58,187,320	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,167,864 - 58,168,108	UniSTS

REN11357

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,466,839 - 61,467,074	UniSTS	GRCh37
Build 36	18	59,617,819 - 59,618,054	RGD	NCBI36
Celera	18	58,187,297 - 58,187,532	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,168,085 - 58,168,320	UniSTS

REN11358

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,467,046 - 61,467,290	UniSTS	GRCh37
Build 36	18	59,618,026 - 59,618,270	RGD	NCBI36
Celera	18	58,187,504 - 58,187,748	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,168,292 - 58,168,536	UniSTS

REN11359

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,467,269 - 61,467,523	UniSTS	GRCh37
Build 36	18	59,618,249 - 59,618,503	RGD	NCBI36
Celera	18	58,187,727 - 58,187,981	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,168,515 - 58,168,769	UniSTS

REN11360

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,467,347 - 61,467,604	UniSTS	GRCh37
Build 36	18	59,618,327 - 59,618,584	RGD	NCBI36
Celera	18	58,187,805 - 58,188,062	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,168,593 - 58,168,850	UniSTS

REN11361

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,467,583 - 61,467,822	UniSTS	GRCh37
Build 36	18	59,618,563 - 59,618,802	RGD	NCBI36
Celera	18	58,188,041 - 58,188,280	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,168,829 - 58,169,068	UniSTS

REN11362

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,467,744 - 61,468,001	UniSTS	GRCh37
Build 36	18	59,618,724 - 59,618,981	RGD	NCBI36
Celera	18	58,188,202 - 58,188,459	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,168,990 - 58,169,247	UniSTS

REN11363

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,467,979 - 61,468,220	UniSTS	GRCh37
Build 36	18	59,618,959 - 59,619,200	RGD	NCBI36
Celera	18	58,188,437 - 58,188,678	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,169,225 - 58,169,466	UniSTS

REN11364

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,468,185 - 61,468,428	UniSTS	GRCh37
Build 36	18	59,619,165 - 59,619,408	RGD	NCBI36
Celera	18	58,188,643 - 58,188,886	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,169,431 - 58,169,674	UniSTS

REN11365

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,468,408 - 61,468,676	UniSTS	GRCh37
Build 36	18	59,619,388 - 59,619,656	RGD	NCBI36
Celera	18	58,188,866 - 58,189,134	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,169,654 - 58,169,922	UniSTS

REN11366

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,468,658 - 61,468,914	UniSTS	GRCh37
Build 36	18	59,619,638 - 59,619,894	RGD	NCBI36
Celera	18	58,189,116 - 58,189,372	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,169,904 - 58,170,160	UniSTS

REN11367

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,468,896 - 61,469,154	UniSTS	GRCh37
Build 36	18	59,619,876 - 59,620,134	RGD	NCBI36
Celera	18	58,189,354 - 58,189,612	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,170,142 - 58,170,400	UniSTS

REN11368

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,469,152 - 61,469,401	UniSTS	GRCh37
Build 36	18	59,620,132 - 59,620,381	RGD	NCBI36
Celera	18	58,189,610 - 58,189,859	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,170,398 - 58,170,647	UniSTS

REN11369

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,469,372 - 61,469,607	UniSTS	GRCh37
Build 36	18	59,620,352 - 59,620,587	RGD	NCBI36
Celera	18	58,189,830 - 58,190,065	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,170,618 - 58,170,853	UniSTS

REN11370

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,469,556 - 61,469,781	UniSTS	GRCh37
Build 36	18	59,620,536 - 59,620,761	RGD	NCBI36
Celera	18	58,190,014 - 58,190,239	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,170,802 - 58,171,027	UniSTS

REN11371

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,469,752 - 61,470,001	UniSTS	GRCh37
Build 36	18	59,620,732 - 59,620,981	RGD	NCBI36
Celera	18	58,190,210 - 58,190,459	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,170,998 - 58,171,247	UniSTS

REN11372

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,469,978 - 61,470,247	UniSTS	GRCh37
Build 36	18	59,620,958 - 59,621,227	RGD	NCBI36
Celera	18	58,190,436 - 58,190,705	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,171,224 - 58,171,493	UniSTS

REN11373

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,470,222 - 61,470,475	UniSTS	GRCh37
Build 36	18	59,621,202 - 59,621,455	RGD	NCBI36
Celera	18	58,190,680 - 58,190,933	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,171,468 - 58,171,721	UniSTS

REN11374

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,470,445 - 61,470,686	UniSTS	GRCh37
Build 36	18	59,621,425 - 59,621,666	RGD	NCBI36
Celera	18	58,190,903 - 58,191,144	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,171,691 - 58,171,932	UniSTS

REN11375

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,470,648 - 61,470,893	UniSTS	GRCh37
Build 36	18	59,621,628 - 59,621,873	RGD	NCBI36
Celera	18	58,191,106 - 58,191,351	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,171,894 - 58,172,139	UniSTS

REN11376

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,470,853 - 61,471,103	UniSTS	GRCh37
Build 36	18	59,621,833 - 59,622,083	RGD	NCBI36
Celera	18	58,191,311 - 58,191,561	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,172,099 - 58,172,349	UniSTS

REN11377

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,471,080 - 61,471,337	UniSTS	GRCh37
Build 36	18	59,622,060 - 59,622,317	RGD	NCBI36
Celera	18	58,191,538 - 58,191,795	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,172,326 - 58,172,583	UniSTS

REN11378

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,471,329 - 61,471,577	UniSTS	GRCh37
Build 36	18	59,622,309 - 59,622,557	RGD	NCBI36
Celera	18	58,191,787 - 58,192,035	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,172,575 - 58,172,823	UniSTS

REN11379

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,471,551 - 61,471,781	UniSTS	GRCh37
Build 36	18	59,622,531 - 59,622,761	RGD	NCBI36
Celera	18	58,192,009 - 58,192,239	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,172,797 - 58,173,027	UniSTS

REN11380

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,471,759 - 61,472,002	UniSTS	GRCh37
Build 36	18	59,622,739 - 59,622,982	RGD	NCBI36
Celera	18	58,192,217 - 58,192,460	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,173,005 - 58,173,248	UniSTS

REN11381

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,471,976 - 61,472,206	UniSTS	GRCh37
Build 36	18	59,622,956 - 59,623,186	RGD	NCBI36
Celera	18	58,192,434 - 58,192,664	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,173,222 - 58,173,452	UniSTS

REN11382

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,472,165 - 61,472,410	UniSTS	GRCh37
Build 36	18	59,623,145 - 59,623,390	RGD	NCBI36
Celera	18	58,192,623 - 58,192,868	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,173,411 - 58,173,656	UniSTS

REN11383

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,472,400 - 61,472,647	UniSTS	GRCh37
Build 36	18	59,623,380 - 59,623,627	RGD	NCBI36
Celera	18	58,192,858 - 58,193,105	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,173,646 - 58,173,893	UniSTS

REN11384

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,472,630 - 61,472,880	UniSTS	GRCh37
Build 36	18	59,623,610 - 59,623,860	RGD	NCBI36
Celera	18	58,193,088 - 58,193,338	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,173,876 - 58,174,126	UniSTS

REN11385

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,472,814 - 61,473,064	UniSTS	GRCh37
Build 36	18	59,623,794 - 59,624,044	RGD	NCBI36
Celera	18	58,193,272 - 58,193,522	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,174,060 - 58,174,310	UniSTS

D18S42

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,424,020 - 61,424,201	UniSTS	GRCh37
Build 36	18	59,575,000 - 59,575,181	RGD	NCBI36
Celera	18	58,144,528 - 58,144,715	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,125,336 - 58,125,523	UniSTS
Whitehead-YAC Contig Map	18		UniSTS

stSG619420

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,419,222 - 61,420,287	UniSTS	GRCh37
Build 36	18	59,570,202 - 59,571,267	RGD	NCBI36
Celera	18	58,139,732 - 58,140,797	RGD
HuRef	18	58,120,539 - 58,121,604	UniSTS

stSG619421

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,420,268 - 61,421,349	UniSTS	GRCh37
Build 36	18	59,571,248 - 59,572,329	RGD	NCBI36
Celera	18	58,140,778 - 58,141,859	RGD
HuRef	18	58,121,585 - 58,122,666	UniSTS

stSG619422

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,421,331 - 61,422,619	UniSTS	GRCh37
Build 36	18	59,572,311 - 59,573,599	RGD	NCBI36
Celera	18	58,141,841 - 58,143,129	RGD
HuRef	18	58,122,648 - 58,123,937	UniSTS

stSG619423

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,422,618 - 61,424,041	UniSTS	GRCh37
Build 36	18	59,573,598 - 59,575,021	RGD	NCBI36
Celera	18	58,143,128 - 58,144,549	RGD
HuRef	18	58,123,936 - 58,125,357	UniSTS

stSG619424

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,424,022 - 61,425,084	UniSTS	GRCh37
Build 36	18	59,575,002 - 59,576,064	RGD	NCBI36
Celera	18	58,144,530 - 58,145,598	RGD
HuRef	18	58,125,338 - 58,126,406	UniSTS

stSG619425

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,425,066 - 61,426,084	UniSTS	GRCh37
Build 36	18	59,576,046 - 59,577,064	RGD	NCBI36
Celera	18	58,145,580 - 58,146,598	RGD
HuRef	18	58,126,388 - 58,127,406	UniSTS

stSG619426

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,425,796 - 61,426,849	UniSTS	GRCh37
Build 36	18	59,576,776 - 59,577,829	RGD	NCBI36
Celera	18	58,146,310 - 58,147,363	RGD
HuRef	18	58,127,118 - 58,128,171	UniSTS

stSG619427

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,429,153 - 61,430,221	UniSTS	GRCh37
Build 36	18	59,580,133 - 59,581,201	RGD	NCBI36
Celera	18	58,149,667 - 58,150,735	RGD
HuRef	18	58,130,475 - 58,131,543	UniSTS

stSG619428

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,430,306 - 61,431,620	UniSTS	GRCh37
Build 36	18	59,581,286 - 59,582,600	RGD	NCBI36
Celera	18	58,150,820 - 58,152,134	RGD
HuRef	18	58,131,628 - 58,132,942	UniSTS

stSG619429

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,431,617 - 61,433,113	UniSTS	GRCh37
Build 36	18	59,582,597 - 59,584,093	RGD	NCBI36
Celera	18	58,152,131 - 58,153,627	RGD
HuRef	18	58,132,939 - 58,134,435	UniSTS

stSG619430

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,433,152 - 61,434,340	UniSTS	GRCh37
Build 36	18	59,584,132 - 59,585,320	RGD	NCBI36
Celera	18	58,153,666 - 58,154,854	RGD
HuRef	18	58,134,474 - 58,135,662	UniSTS

stSG619431

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,433,780 - 61,434,783	UniSTS	GRCh37
Build 36	18	59,584,760 - 59,585,763	RGD	NCBI36
Celera	18	58,154,294 - 58,155,297	RGD

stSG619432

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,436,914 - 61,438,121	UniSTS	GRCh37
Build 36	18	59,587,894 - 59,589,101	RGD	NCBI36
Celera	18	58,157,429 - 58,158,636	RGD
HuRef	18	58,138,148 - 58,139,355	UniSTS

stSG619434

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,439,562 - 61,440,987	UniSTS	GRCh37
Build 36	18	59,590,542 - 59,591,967	RGD	NCBI36
Celera	18	58,160,079 - 58,161,504	RGD
HuRef	18	58,140,804 - 58,142,229	UniSTS

stSG619435

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,440,967 - 61,442,405	UniSTS	GRCh37
Build 36	18	59,591,947 - 59,593,385	RGD	NCBI36
Celera	18	58,161,484 - 58,162,922	RGD
HuRef	18	58,142,209 - 58,143,647	UniSTS

stSG619436

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,442,386 - 61,443,697	UniSTS	GRCh37
Build 36	18	59,593,366 - 59,594,677	RGD	NCBI36
Celera	18	58,162,903 - 58,164,214	RGD
HuRef	18	58,143,628 - 58,144,939	UniSTS

stSG619437

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,443,678 - 61,444,725	UniSTS	GRCh37
Build 36	18	59,594,658 - 59,595,705	RGD	NCBI36
Celera	18	58,164,195 - 58,165,242	RGD
HuRef	18	58,144,920 - 58,145,967	UniSTS

stSG619438

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,444,706 - 61,446,050	UniSTS	GRCh37
Build 36	18	59,595,686 - 59,597,030	RGD	NCBI36
Celera	18	58,165,223 - 58,166,556	RGD
HuRef	18	58,145,948 - 58,147,280	UniSTS

stSG619439

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,446,048 - 61,447,472	UniSTS	GRCh37
Build 36	18	59,597,028 - 59,598,452	RGD	NCBI36
Celera	18	58,166,554 - 58,167,978	RGD
HuRef	18	58,147,278 - 58,148,702	UniSTS

stSG619440

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,447,453 - 61,448,454	UniSTS	GRCh37
Build 36	18	59,598,433 - 59,599,434	RGD	NCBI36
Celera	18	58,167,959 - 58,168,960	RGD
HuRef	18	58,148,683 - 58,149,684	UniSTS

stSG619441

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,448,435 - 61,449,600	UniSTS	GRCh37
Build 36	18	59,599,415 - 59,600,580	RGD	NCBI36
Celera	18	58,168,941 - 58,170,106	RGD
HuRef	18	58,149,665 - 58,150,830	UniSTS

stSG619442

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,449,581 - 61,450,723	UniSTS	GRCh37
Build 36	18	59,600,561 - 59,601,703	RGD	NCBI36
Celera	18	58,170,087 - 58,171,199	RGD
HuRef	18	58,150,811 - 58,151,923	UniSTS

stSG619443

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,450,704 - 61,452,122	UniSTS	GRCh37
Build 36	18	59,601,684 - 59,603,102	RGD	NCBI36
Celera	18	58,171,180 - 58,172,598	RGD
HuRef	18	58,151,904 - 58,153,322	UniSTS

stSG619447

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,454,986 - 61,456,285	UniSTS	GRCh37
Build 36	18	59,605,966 - 59,607,265	RGD	NCBI36
Celera	18	58,175,444 - 58,176,743	RGD
HuRef	18	58,156,234 - 58,157,533	UniSTS

stSG619448

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,456,264 - 61,456,443	UniSTS	GRCh37
Build 36	18	59,607,244 - 59,607,423	RGD	NCBI36
Celera	18	58,176,722 - 58,176,901	RGD
HuRef	18	58,157,512 - 58,157,691	UniSTS

stSG619449

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,456,444 - 61,457,554	UniSTS	GRCh37
Build 36	18	59,607,424 - 59,608,534	RGD	NCBI36
Celera	18	58,176,902 - 58,178,012	RGD
HuRef	18	58,157,692 - 58,158,802	UniSTS

stSG619451

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,458,635 - 61,459,661	UniSTS	GRCh37
Build 36	18	59,609,615 - 59,610,641	RGD	NCBI36
Celera	18	58,179,093 - 58,180,119	RGD
HuRef	18	58,159,883 - 58,160,909	UniSTS

stSG619452

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,459,641 - 61,460,805	UniSTS	GRCh37
Build 36	18	59,610,621 - 59,611,785	RGD	NCBI36
Celera	18	58,180,099 - 58,181,263	RGD
HuRef	18	58,160,889 - 58,162,053	UniSTS

stSG619453

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,460,786 - 61,462,012	UniSTS	GRCh37
Build 36	18	59,611,766 - 59,612,992	RGD	NCBI36
Celera	18	58,181,244 - 58,182,469	RGD
HuRef	18	58,162,034 - 58,163,257	UniSTS

stSG619454

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,461,993 - 61,463,274	UniSTS	GRCh37
Build 36	18	59,612,973 - 59,614,254	RGD	NCBI36
Celera	18	58,182,450 - 58,183,731	RGD
HuRef	18	58,163,238 - 58,164,520	UniSTS

stSG619455

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,463,325 - 61,464,422	UniSTS	GRCh37
Build 36	18	59,614,305 - 59,615,402	RGD	NCBI36
Celera	18	58,183,782 - 58,184,879	RGD
HuRef	18	58,164,571 - 58,165,668	UniSTS

stSG619456

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,464,403 - 61,465,473	UniSTS	GRCh37
Build 36	18	59,615,383 - 59,616,453	RGD	NCBI36
Celera	18	58,184,860 - 58,185,930	RGD
HuRef	18	58,165,649 - 58,166,719	UniSTS

stSG619457

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,465,454 - 61,466,917	UniSTS	GRCh37
Build 36	18	59,616,434 - 59,617,897	RGD	NCBI36
Celera	18	58,185,911 - 58,187,375	RGD
HuRef	18	58,166,700 - 58,168,163	UniSTS

stSG619458

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,466,898 - 61,468,231	UniSTS	GRCh37
Build 36	18	59,617,878 - 59,619,211	RGD	NCBI36
Celera	18	58,187,356 - 58,188,689	RGD
HuRef	18	58,168,144 - 58,169,477	UniSTS

stSG619459

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,468,215 - 61,469,482	UniSTS	GRCh37
Build 36	18	59,619,195 - 59,620,462	RGD	NCBI36
Celera	18	58,188,673 - 58,189,940	RGD
HuRef	18	58,169,461 - 58,170,728	UniSTS

stSG619460

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,469,464 - 61,470,776	UniSTS	GRCh37
Build 36	18	59,620,444 - 59,621,756	RGD	NCBI36
Celera	18	58,189,922 - 58,191,234	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,170,710 - 58,172,022	UniSTS

stSG619461

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	18	61,470,757 - 61,471,810	UniSTS	GRCh37
Build 36	18	59,621,737 - 59,622,790	RGD	NCBI36
Celera	18	58,191,215 - 58,192,268	RGD
Cytogenetic Map	18	q21.33	UniSTS
HuRef	18	58,172,003 - 58,173,056	UniSTS

Expression

RNA-SEQ Expression

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	renal system	reproductive system	respiratory system	sensory system
1083	1479	2176	1510	3108	789	1415	5	282	755	139	1999	4158	4079	41	2015	664	1298	1042	157

Sequence

Nucleotide Sequences


RefSeq Transcripts	NG_034150	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001040147	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001261830	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001261831	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_003784	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024451278	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319290	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC069356	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC072051	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF027866	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK290673	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK290876	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK300828	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC069417	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC069442	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC069547	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC106743	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC106744	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BP332064	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX641156	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CD701612	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CD702645	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471096	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068260	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	D88575	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA577978	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF456427	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000336429 ⟹ ENSP00000337212

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	63,753,042 - 63,805,376 (+)	Ensembl

Ensembl Acc Id:

ENST00000398019 ⟹ ENSP00000381101

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	63,775,418 - 63,805,370 (+)	Ensembl

Ensembl Acc Id:

ENST00000425392 ⟹ ENSP00000397301

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	63,752,935 - 63,796,312 (+)	Ensembl

Ensembl Acc Id:

ENST00000431370 ⟹ ENSP00000393947

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	63,777,977 - 63,796,313 (+)	Ensembl

Ensembl Acc Id:

ENST00000447428 ⟹ ENSP00000402362

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	63,777,777 - 63,798,643 (+)	Ensembl

Ensembl Acc Id:

ENST00000540675 ⟹ ENSP00000444572

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	63,775,375 - 63,805,376 (+)	Ensembl

Ensembl Acc Id:

ENST00000546027 ⟹ ENSP00000444861

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	63,777,777 - 63,805,376 (+)	Ensembl

Ensembl Acc Id:

ENST00000894156 ⟹ ENSP00000564215

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	63,753,042 - 63,805,376 (+)	Ensembl

Ensembl Acc Id:

ENST00000894157 ⟹ ENSP00000564216

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	63,758,720 - 63,805,376 (+)	Ensembl

Ensembl Acc Id:

ENST00001132717 ⟹ ENSP00000812049

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	18	63,775,375 - 63,805,376 (+)	Ensembl

RefSeq Acc Id:

NM_001040147 ⟹ NP_001035237

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	18	63,753,057 - 63,805,370 (+)	NCBI
GRCh37	18	61,420,281 - 61,472,610 (+)	NCBI
Build 36	18	59,571,257 - 59,623,583 (+)	NCBI Archive
HuRef	18	58,121,598 - 58,173,856 (+)	NCBI
CHM1_1	18	61,416,473 - 61,468,833 (+)	NCBI
T2T-CHM13v2.0	18	63,958,110 - 64,010,475 (+)	NCBI

Sequence:

show sequence

AGGAGGTAGGAGGCAGGAGGAACTGAAGCCCAGCTGTGAAGGCCGCAGACTGCAGTGAGAGGAG
GCTGCACTCCATTTTGCAATGGCCTCCCTTGCTGCAGCAAATGCAGAGTTTTGCTTCAACCTGT
TCAGAGAGATGGATGACAATCAAGGAAATGGAAATGTGTTCTTTTCCTCTCTGAGCCTCTTCGC
TGCCCTGGCCCTGGTCCGCTTGGGCGCTCAAGATGACTCCCTCTCTCAGATTGATAAGTTGCTT
CATGTTAACACTGCCTCAGGATATGGAAACTCTTCTAATAGTCAGTCAGGGCTCCAGTCTCAAC
TGAAAAGAGTTTTTTCTGATATAAATGCATCCCACAAGGATTATGATCTCAGCATTGTGAATGG
GCTTTTTGCTGAAAAAGTGTATGGCTTTCATAAGGACTACATTGAGTGTGCCGAAAAATTATAC
GATGCCAAAGTGGAGCGAGTTGACTTTACGAATCATTTAGAAGACACTAGACGTAATATTAATA
AGTGGGTTGAAAATGAAACACATGGCAAAATCAAGAACGTGATTGGTGAAGGTGGCATAAGCTC
ATCTGCTGTAATGGTGCTGGTGAATGCTGTGTACTTCAAAGGCAAGTGGCAATCAGCCTTCACC
AAGAGCGAAACCATAAATTGCCATTTCAAATCTCCCAAGTGCTCTGGGAAGGCAGTCGCCATGA
TGCATCAGGAACGGAAGTTCAATTTGTCTGTTATTGAGGACCCATCAATGAAGATTCTTGAGCT
CAGATACAATGGTGGCATAAACATGTACGTTCTGCTGCCTGAGAATGACCTCTCTGAAATTGAA
AACAAACTGACCTTTCAGAATCTAATGGAATGGACCAATCCAAGGCGAATGACCTCTAAGTATG
TTGAGGTATTTTTTCCTCAGTTCAAGATAGAGAAGAATTATGAAATGAAACAATATTTGAGAGC
CCTAGGGCTGAAAGATATCTTTGATGAATCCAAAGCAGATCTCTCTGGGATTGCTTCGGGGGGT
CGTCTGTATATATCAAGGATGATGCACAAATCTTACATAGAGGTCACTGAGGAGGGCACCGAGG
CTACTGCTGCCACAGGAAGTAATATTGTAGAAAAGCAACTCCCTCAGTCCACGCTGTTTAGAGC
TGACCACCCATTCCTATTTGTTATCAGGAAGGATGACATCATCTTATTCAGTGGCAAAGTTTCT
TGCCCTTGAAAATCCAATTGGTTTCTGTTATAGCAGTCCCCACAACATCAAAGAACCACCACAA
GTCAATAGATTTGAGTTTAATTGGAAAAATGTGGTGTTTCCTTTGAGTTTATTTCTTCCTAACA
TTGGTCAGCAGATGACACTGGTGACTTGACCCTTCCTAGACACCTGGTTGATTGTCCTGATCCC
TGCTCTTAGCATTCTACCACCATGTGTCTCACCCATTTCTAATTTCATTGTCTTTCTTCCCACG
CTCATTTCTATCATTCTCCCCCATGACCCGTCTGGAAATTATGGAGAGTGCTCAACTGGTAAGG
AGAACGTAGAAGTAGCCCTAGGGATCCTTTTTGAAACTCTACAGTTATCGCAGATATTCTAGCT
TCATTGTAAGCAATCTAGGAAATAAGCCCTGCTGCTTTCTAGAAATAAGTGTGAAGGATAAATT
TTCTTTGTTGACCTATGAAGATTTTAGAGTTTACCTTCATATGTTTGATTTTAAATCAGTGTAT
AATCTAGATGGTAAAAAATGTGAAATTGGGATTAGGGACCAACCAAAATATTTCATTAATGCTT
TCAATTGACAAATTTTGGTCTTTCTTTGATAAGACAATATGTACATAGTTTTTTCAAATATTAA
AGATCTTTTAACTGTTGGCAGTTGTTATCTACAGAATCATATCTCATATGCTGTGTAGTTTATA
AGTTTTTTCTCTATTTATCAGAATAAAGAAATACAACATA

hide sequence

RefSeq Acc Id:

NM_001261830 ⟹ NP_001248759

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	18	63,777,781 - 63,805,370 (+)	NCBI
GRCh37	18	61,420,281 - 61,472,610 (+)	NCBI
HuRef	18	58,121,598 - 58,173,856 (+)	NCBI
CHM1_1	18	61,441,234 - 61,468,833 (+)	NCBI
T2T-CHM13v2.0	18	63,982,838 - 64,010,475 (+)	NCBI

Sequence:

show sequence

AGACTCACCCAACCAGCGGCCAACTTCCTCTATGAAGACAGTAAGGCTGCACTCCATTTTGCAA
TGGCCTCCCTTGCTGCAGCAAATGCAGAGTTTTGCTTCAACCTGTTCAGAGAGATGGATGACAA
TCAAGGAAATGGAAATGTGTTCTTTTCCTCTCTGAGCCTCTTCGCTGCCCTGGCCCTGGTCCGC
TTGGGCGCTCAAGATGACTCCCTCTCTCAGATTGATAAGTTGCTTCATGTTAACACTGCCTCAG
GATATGGAAACTCTTCTAATAGTCAGTCAGGGCTCCAGTCTCAACTGAAAAGAGTTTTTTCTGA
TATAAATGCATCCCACAAGGATTATGATCTCAGCATTGTGAATGGGCTTTTTGCTGAAAAAGTG
TATGGCTTTCATAAGGACTACATTGAGTGTGCCGAAAAATTATACGATGCCAAAGTGGAGCGAG
TTGACTTTACGAATCATTTAGAAGACACTAGACGTAATATTAATAAGTGGGTTGAAAATGAAAC
ACATGGCAAAATCAAGAACGTGATTGGTGAAGGTGGCATAAGCTCATCTGCTGTAATGGTGCTG
GTGAATGCTGTGTACTTCAAAGGCAAGTGGCAATCAGCCTTCACCAAGAGCGAAACCATAAATT
GCCATTTCAAATCTCCCAAGTGCTCTGGGAAGGCAGTCGCCATGATGCATCAGGAACGGAAGTT
CAATTTGTCTGTTATTGAGGACCCATCAATGAAGATTCTTGAGCTCAGATACAATGGTGGCATA
AACATGTACGTTCTGCTGCCTGAGAATGACCTCTCTGAAATTGAAAACAAACTGACCTTTCAGA
ATCTAATGGAATGGACCAATCCAAGGCGAATGACCTCTAAGTATGTTGAGGTATTTTTTCCTCA
GTTCAAGATAGAGAAGAATTATGAAATGAAACAATATTTGAGAGCCCTAGGGCTGAAAGATATC
TTTGATGAATCCAAAGCAGATCTCTCTGGGATTGCTTCGGGGGGTCGTCTGTATATATCAAGGA
TGATGCACAAATCTTACATAGAGGTCACTGAGGAGGGCACCGAGGCTACTGCTGCCACAGGAAG
TAATATTGTAGAAAAGCAACTCCCTCAGTCCACGCTGTTTAGAGCTGACCACCCATTCCTATTT
GTTATCAGGAAGGATGACATCATCTTATTCAGTGGCAAAGTTTCTTGCCCTTGAAAATCCAATT
GGTTTCTGTTATAGCAGTCCCCACAACATCAAAGAACCACCACAAGTCAATAGATTTGAGTTTA
ATTGGAAAAATGTGGTGTTTCCTTTGAGTTTATTTCTTCCTAACATTGGTCAGCAGATGACACT
GGTGACTTGACCCTTCCTAGACACCTGGTTGATTGTCCTGATCCCTGCTCTTAGCATTCTACCA
CCATGTGTCTCACCCATTTCTAATTTCATTGTCTTTCTTCCCACGCTCATTTCTATCATTCTCC
CCCATGACCCGTCTGGAAATTATGGAGAGTGCTCAACTGGTAAGGAGAACGTAGAAGTAGCCCT
AGGGATCCTTTTTGAAACTCTACAGTTATCGCAGATATTCTAGCTTCATTGTAAGCAATCTAGG
AAATAAGCCCTGCTGCTTTCTAGAAATAAGTGTGAAGGATAAATTTTCTTTGTTGACCTATGAA
GATTTTAGAGTTTACCTTCATATGTTTGATTTTAAATCAGTGTATAATCTAGATGGTAAAAAAT
GTGAAATTGGGATTAGGGACCAACCAAAATATTTCATTAATGCTTTCAATTGACAAATTTTGGT
CTTTCTTTGATAAGACAATATGTACATAGTTTTTTCAAATATTAAAGATCTTTTAACTGTTGGC
AGTTGTTATCTACAGAATCATATCTCATATGCTGTGTAGTTTATAAGTTTTTTCTCTATTTATC
AGAATAAAGAAATACAACATA

hide sequence

RefSeq Acc Id:

NM_001261831 ⟹ NP_001248760

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	18	63,775,418 - 63,805,370 (+)	NCBI
GRCh37	18	61,420,281 - 61,472,610 (+)	NCBI
HuRef	18	58,121,598 - 58,173,856 (+)	NCBI
CHM1_1	18	61,438,832 - 61,468,833 (+)	NCBI
T2T-CHM13v2.0	18	63,980,475 - 64,010,475 (+)	NCBI

Sequence:

show sequence

ATCAATAAGCAGCTGCCTGTGCAGAGTGCAGGCTGCACCTTTGGACAGCCTTTAAAACTGAATT
CTCAGAATTTTAGAACAAATTTTTGTCTAGAAATGCTGACTTTGGTTCATTAGGTAGTGGTAAA
ACAGGCTCCCTTCGAAGCTCTCCTTCATCACCTTCCTAAGTGCATGGGGGAAAATACCTAGGGC
TCAACAGTCTTGAGAAGTGTGGAAACATTTTCTTTGTGAGTGAGAACAGATCACCTAGAGAAAG
GAGACCAGATTCCCATCACTGCTTCTGGGTATCAGATGCTAGCGCTGCACTCCATTTTGCAATG
GCCTCCCTTGCTGCAGCAAATGCAGAGTTTTGCTTCAACCTGTTCAGAGAGATGGATGACAATC
AAGGAAATGGAAATGTGTTCTTTTCCTCTCTGAGCCTCTTCGCTGCCCTGGCCCTGGTCCGCTT
GGGCGCTCAAGATGACTCCCTCTCTCAGATTGATAAGTCAGGGCTCCAGTCTCAACTGAAAAGA
GTTTTTTCTGATATAAATGCATCCCACAAGGATTATGATCTCAGCATTGTGAATGGGCTTTTTG
CTGAAAAAGTGTATGGCTTTCATAAGGACTACATTGAGTGTGCCGAAAAATTATACGATGCCAA
AGTGGAGCGAGTTGACTTTACGAATCATTTAGAAGACACTAGACGTAATATTAATAAGTGGGTT
GAAAATGAAACACATGGCAAAATCAAGAACGTGATTGGTGAAGGTGGCATAAGCTCATCTGCTG
TAATGGTGCTGGTGAATGCTGTGTACTTCAAAGGCAAGTGGCAATCAGCCTTCACCAAGAGCGA
AACCATAAATTGCCATTTCAAATCTCCCAAGTGCTCTGGGAAGGCAGTCGCCATGATGCATCAG
GAACGGAAGTTCAATTTGTCTGTTATTGAGGACCCATCAATGAAGATTCTTGAGCTCAGATACA
ATGGTGGCATAAACATGTACGTTCTGCTGCCTGAGAATGACCTCTCTGAAATTGAAAACAAACT
GACCTTTCAGAATCTAATGGAATGGACCAATCCAAGGCGAATGACCTCTAAGTATGTTGAGGTA
TTTTTTCCTCAGTTCAAGATAGAGAAGAATTATGAAATGAAACAATATTTGAGAGCCCTAGGGC
TGAAAGATATCTTTGATGAATCCAAAGCAGATCTCTCTGGGATTGCTTCGGGGGGTCGTCTGTA
TATATCAAGGATGATGCACAAATCTTACATAGAGGTCACTGAGGAGGGCACCGAGGCTACTGCT
GCCACAGGAAGTAATATTGTAGAAAAGCAACTCCCTCAGTCCACGCTGTTTAGAGCTGACCACC
CATTCCTATTTGTTATCAGGAAGGATGACATCATCTTATTCAGTGGCAAAGTTTCTTGCCCTTG
AAAATCCAATTGGTTTCTGTTATAGCAGTCCCCACAACATCAAAGAACCACCACAAGTCAATAG
ATTTGAGTTTAATTGGAAAAATGTGGTGTTTCCTTTGAGTTTATTTCTTCCTAACATTGGTCAG
CAGATGACACTGGTGACTTGACCCTTCCTAGACACCTGGTTGATTGTCCTGATCCCTGCTCTTA
GCATTCTACCACCATGTGTCTCACCCATTTCTAATTTCATTGTCTTTCTTCCCACGCTCATTTC
TATCATTCTCCCCCATGACCCGTCTGGAAATTATGGAGAGTGCTCAACTGGTAAGGAGAACGTA
GAAGTAGCCCTAGGGATCCTTTTTGAAACTCTACAGTTATCGCAGATATTCTAGCTTCATTGTA
AGCAATCTAGGAAATAAGCCCTGCTGCTTTCTAGAAATAAGTGTGAAGGATAAATTTTCTTTGT
TGACCTATGAAGATTTTAGAGTTTACCTTCATATGTTTGATTTTAAATCAGTGTATAATCTAGA
TGGTAAAAAATGTGAAATTGGGATTAGGGACCAACCAAAATATTTCATTAATGCTTTCAATTGA
CAAATTTTGGTCTTTCTTTGATAAGACAATATGTACATAGTTTTTTCAAATATTAAAGATCTTT
TAACTGTTGGCAGTTGTTATCTACAGAATCATATCTCATATGCTGTGTAGTTTATAAGTTTTTT
CTCTATTTATCAGAATAAAGAAATACAACATA

hide sequence

RefSeq Acc Id:

NM_003784 ⟹ NP_003775

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	18	63,775,418 - 63,805,370 (+)	NCBI
GRCh37	18	61,420,281 - 61,472,610 (+)	NCBI
Build 36	18	59,593,592 - 59,623,584 (+)	NCBI Archive
HuRef	18	58,121,598 - 58,173,856 (+)	NCBI
CHM1_1	18	61,438,832 - 61,468,833 (+)	NCBI
T2T-CHM13v2.0	18	63,980,475 - 64,010,475 (+)	NCBI

Sequence:

show sequence

ATCAATAAGCAGCTGCCTGTGCAGAGTGCAGGCTGCACCTTTGGACAGCCTTTAAAACTGAATT
CTCAGAATTTTAGAACAAATTTTTGTCTAGAAATGCTGACTTTGGTTCATTAGGTAGTGGTAAA
ACAGGCTCCCTTCGAAGCTCTCCTTCATCACCTTCCTAAGTGCATGGGGGAAAATACCTAGGGC
TCAACAGTCTTGAGAAGTGTGGAAACATTTTCTTTGTGAGTGAGAACAGATCACCTAGAGAAAG
GAGACCAGATTCCCATCACTGCTTCTGGGTATCAGATGCTAGCGCTGCACTCCATTTTGCAATG
GCCTCCCTTGCTGCAGCAAATGCAGAGTTTTGCTTCAACCTGTTCAGAGAGATGGATGACAATC
AAGGAAATGGAAATGTGTTCTTTTCCTCTCTGAGCCTCTTCGCTGCCCTGGCCCTGGTCCGCTT
GGGCGCTCAAGATGACTCCCTCTCTCAGATTGATAAGTTGCTTCATGTTAACACTGCCTCAGGA
TATGGAAACTCTTCTAATAGTCAGTCAGGGCTCCAGTCTCAACTGAAAAGAGTTTTTTCTGATA
TAAATGCATCCCACAAGGATTATGATCTCAGCATTGTGAATGGGCTTTTTGCTGAAAAAGTGTA
TGGCTTTCATAAGGACTACATTGAGTGTGCCGAAAAATTATACGATGCCAAAGTGGAGCGAGTT
GACTTTACGAATCATTTAGAAGACACTAGACGTAATATTAATAAGTGGGTTGAAAATGAAACAC
ATGGCAAAATCAAGAACGTGATTGGTGAAGGTGGCATAAGCTCATCTGCTGTAATGGTGCTGGT
GAATGCTGTGTACTTCAAAGGCAAGTGGCAATCAGCCTTCACCAAGAGCGAAACCATAAATTGC
CATTTCAAATCTCCCAAGTGCTCTGGGAAGGCAGTCGCCATGATGCATCAGGAACGGAAGTTCA
ATTTGTCTGTTATTGAGGACCCATCAATGAAGATTCTTGAGCTCAGATACAATGGTGGCATAAA
CATGTACGTTCTGCTGCCTGAGAATGACCTCTCTGAAATTGAAAACAAACTGACCTTTCAGAAT
CTAATGGAATGGACCAATCCAAGGCGAATGACCTCTAAGTATGTTGAGGTATTTTTTCCTCAGT
TCAAGATAGAGAAGAATTATGAAATGAAACAATATTTGAGAGCCCTAGGGCTGAAAGATATCTT
TGATGAATCCAAAGCAGATCTCTCTGGGATTGCTTCGGGGGGTCGTCTGTATATATCAAGGATG
ATGCACAAATCTTACATAGAGGTCACTGAGGAGGGCACCGAGGCTACTGCTGCCACAGGAAGTA
ATATTGTAGAAAAGCAACTCCCTCAGTCCACGCTGTTTAGAGCTGACCACCCATTCCTATTTGT
TATCAGGAAGGATGACATCATCTTATTCAGTGGCAAAGTTTCTTGCCCTTGAAAATCCAATTGG
TTTCTGTTATAGCAGTCCCCACAACATCAAAGAACCACCACAAGTCAATAGATTTGAGTTTAAT
TGGAAAAATGTGGTGTTTCCTTTGAGTTTATTTCTTCCTAACATTGGTCAGCAGATGACACTGG
TGACTTGACCCTTCCTAGACACCTGGTTGATTGTCCTGATCCCTGCTCTTAGCATTCTACCACC
ATGTGTCTCACCCATTTCTAATTTCATTGTCTTTCTTCCCACGCTCATTTCTATCATTCTCCCC
CATGACCCGTCTGGAAATTATGGAGAGTGCTCAACTGGTAAGGAGAACGTAGAAGTAGCCCTAG
GGATCCTTTTTGAAACTCTACAGTTATCGCAGATATTCTAGCTTCATTGTAAGCAATCTAGGAA
ATAAGCCCTGCTGCTTTCTAGAAATAAGTGTGAAGGATAAATTTTCTTTGTTGACCTATGAAGA
TTTTAGAGTTTACCTTCATATGTTTGATTTTAAATCAGTGTATAATCTAGATGGTAAAAAATGT
GAAATTGGGATTAGGGACCAACCAAAATATTTCATTAATGCTTTCAATTGACAAATTTTGGTCT
TTCTTTGATAAGACAATATGTACATAGTTTTTTCAAATATTAAAGATCTTTTAACTGTTGGCAG
TTGTTATCTACAGAATCATATCTCATATGCTGTGTAGTTTATAAGTTTTTTCTCTATTTATCAG
AATAAAGAAATACAACATA

hide sequence

RefSeq Acc Id:

XM_024451278 ⟹ XP_024307046

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	18	63,774,754 - 63,805,370 (+)	NCBI

Sequence:

show sequence

CCTATCTGAAGCTGCTCAGTTCAGGCTGCACTCCATTTTGCAATGGCCTCCCTTGCTGCAGCAA
ATGCAGAGTTTTGCTTCAACCTGTTCAGAGAGATGGATGACAATCAAGGAAATGGAAATGTGTT
CTTTTCCTCTCTGAGCCTCTTCGCTGCCCTGGCCCTGGTCCGCTTGGGCGCTCAAGATGACTCC
CTCTCTCAGATTGATAAGTTGCTTCATGTTAACACTGCCTCAGGATATGGAAACTCTTCTAATA
GTCAGTCAGGGCTCCAGTCTCAACTGAAAAGAGTTTTTTCTGATATAAATGCATCCCACAAGGA
TTATGATCTCAGCATTGTGAATGGGCTTTTTGCTGAAAAAGTGTATGGCTTTCATAAGGACTAC
ATTGAGTGTGCCGAAAAATTATACGATGCCAAAGTGGAGCGAGTTGACTTTACGAATCATTTAG
AAGACACTAGACGTAATATTAATAAGTGGGTTGAAAATGAAACACATGGCAAAATCAAGAACGT
GATTGGTGAAGGTGGCATAAGCTCATCTGCTGTAATGGTGCTGGTGAATGCTGTGTACTTCAAA
GGCAAGTGGCAATCAGCCTTCACCAAGAGCGAAACCATAAATTGCCATTTCAAATCTCCCAAGT
GCTCTGGGAAGGCAGTCGCCATGATGCATCAGGAACGGAAGTTCAATTTGTCTGTTATTGAGGA
CCCATCAATGAAGATTCTTGAGCTCAGATACAATGGTGGCATAAACATGTACGTTCTGCTGCCT
GAGAATGACCTCTCTGAAATTGAAAACAAACTGACCTTTCAGAATCTAATGGAATGGACCAATC
CAAGGCGAATGACCTCTAAGTATGTTGAGGTATTTTTTCCTCAGTTCAAGATAGAGAAGAATTA
TGAAATGAAACAATATTTGAGAGCCCTAGGGCTGAAAGATATCTTTGATGAATCCAAAGCAGAT
CTCTCTGGGATTGCTTCGGGGGGTCGTCTGTATATATCAAGGATGATGCACAAATCTTACATAG
AGGTCACTGAGGAGGGCACCGAGGCTACTGCTGCCACAGGAAGTAATATTGTAGAAAAGCAACT
CCCTCAGTCCACGCTGTTTAGAGCTGACCACCCATTCCTATTTGTTATCAGGAAGGATGACATC
ATCTTATTCAGTGGCAAAGTTTCTTGCCCTTGAAAATCCAATTGGTTTCTGTTATAGCAGTCCC
CACAACATCAAAGAACCACCACAAGTCAATAGATTTGAGTTTAATTGGAAAAATGTGGTGTTTC
CTTTGAGTTTATTTCTTCCTAACATTGGTCAGCAGATGACACTGGTGACTTGACCCTTCCTAGA
CACCTGGTTGATTGTCCTGATCCCTGCTCTTAGCATTCTACCACCATGTGTCTCACCCATTTCT
AATTTCATTGTCTTTCTTCCCACGCTCATTTCTATCATTCTCCCCCATGACCCGTCTGGAAATT
ATGGAGAGTGCTCAACTGGTAAGGAGAACGTAGAAGTAGCCCTAGGGATCCTTTTTGAAACTCT
ACAGTTATCGCAGATATTCTAGCTTCATTGTAAGCAATCTAGGAAATAAGCCCTGCTGCTTTCT
AGAAATAAGTGTGAAGGATAAATTTTCTTTGTTGACCTATGAAGATTTTAGAGTTTACCTTCAT
ATGTTTGATTTTAAATCAGTGTATAATCTAGATGGTAAAAAATGTGAAATTGGGATTAGGGACC
AACCAAAATATTTCATTAATGCTTTCAATTGACAAATTTTGGTCTTTCTTTGATAAGACAATAT
GTACATAGTTTTTTCAAATATTAAAGATCTTTTAACTGTTGGCAGTTGTTATCTACAGAATCAT
ATCTCATATGCTGTGTAGTTTATAAGTTTTTTCTCTATTTATCAGAATAAAGAAATACAACATA

hide sequence

RefSeq Acc Id:

XM_054319290 ⟹ XP_054175265

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	18	63,979,811 - 64,010,475 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001035237	(Get FASTA)	NCBI Sequence Viewer
	NP_001248759	(Get FASTA)	NCBI Sequence Viewer
	NP_001248760	(Get FASTA)	NCBI Sequence Viewer
	NP_003775	(Get FASTA)	NCBI Sequence Viewer
	XP_024307046	(Get FASTA)	NCBI Sequence Viewer
	XP_054175265	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAC64506	(Get FASTA)	NCBI Sequence Viewer
	AAH69417	(Get FASTA)	NCBI Sequence Viewer
	AAH69442	(Get FASTA)	NCBI Sequence Viewer
	AAH69547	(Get FASTA)	NCBI Sequence Viewer
	AAI06744	(Get FASTA)	NCBI Sequence Viewer
	AAI06745	(Get FASTA)	NCBI Sequence Viewer
	BAA31232	(Get FASTA)	NCBI Sequence Viewer
	BAF83362	(Get FASTA)	NCBI Sequence Viewer
	BAF83565	(Get FASTA)	NCBI Sequence Viewer
	BAG62480	(Get FASTA)	NCBI Sequence Viewer
	CAE46069	(Get FASTA)	NCBI Sequence Viewer
	EAW63159	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000337212
	ENSP00000337212.2
	ENSP00000381101
	ENSP00000381101.2
	ENSP00000444572
	ENSP00000444572.1
	ENSP00000444861
	ENSP00000444861.1
	ENSP00000564215.1
	ENSP00000564216
	ENSP00000564216.1
GenBank Protein	O75635	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001035237 ⟸ NM_001040147
- Peptide Label:	isoform 1
- UniProtKB:	Q1ED45 (UniProtKB/Swiss-Prot), F5GZC0 (UniProtKB/Swiss-Prot), B4DUW8 (UniProtKB/Swiss-Prot), Q3KPG4 (UniProtKB/Swiss-Prot), O75635 (UniProtKB/Swiss-Prot), A8K4B1 (UniProtKB/TrEMBL)
- Sequence:	show sequence MASLAAANAEFCFNLFREMDDNQGNGNVFFSSLSLFAALALVRLGAQDDSLSQIDKLLHVNTAS GYGNSSNSQSGLQSQLKRVFSDINASHKDYDLSIVNGLFAEKVYGFHKDYIECAEKLYDAKVER VDFTNHLEDTRRNINKWVENETHGKIKNVIGEGGISSSAVMVLVNAVYFKGKWQSAFTKSETIN CHFKSPKCSGKAVAMMHQERKFNLSVIEDPSMKILELRYNGGINMYVLLPENDLSEIENKLTFQ NLMEWTNPRRMTSKYVEVFFPQFKIEKNYEMKQYLRALGLKDIFDESKADLSGIASGGRLYISR MMHKSYIEVTEEGTEATAATGSNIVEKQLPQSTLFRADHPFLFVIRKDDIILFSGKVSCP hide sequence

RefSeq Acc Id:	NP_003775 ⟸ NM_003784
- Peptide Label:	isoform 1
- UniProtKB:	Q1ED45 (UniProtKB/Swiss-Prot), F5GZC0 (UniProtKB/Swiss-Prot), B4DUW8 (UniProtKB/Swiss-Prot), Q3KPG4 (UniProtKB/Swiss-Prot), O75635 (UniProtKB/Swiss-Prot), A8K4B1 (UniProtKB/TrEMBL)
- Sequence:	show sequence MASLAAANAEFCFNLFREMDDNQGNGNVFFSSLSLFAALALVRLGAQDDSLSQIDKLLHVNTAS GYGNSSNSQSGLQSQLKRVFSDINASHKDYDLSIVNGLFAEKVYGFHKDYIECAEKLYDAKVER VDFTNHLEDTRRNINKWVENETHGKIKNVIGEGGISSSAVMVLVNAVYFKGKWQSAFTKSETIN CHFKSPKCSGKAVAMMHQERKFNLSVIEDPSMKILELRYNGGINMYVLLPENDLSEIENKLTFQ NLMEWTNPRRMTSKYVEVFFPQFKIEKNYEMKQYLRALGLKDIFDESKADLSGIASGGRLYISR MMHKSYIEVTEEGTEATAATGSNIVEKQLPQSTLFRADHPFLFVIRKDDIILFSGKVSCP hide sequence

RefSeq Acc Id:	NP_001248760 ⟸ NM_001261831
- Peptide Label:	isoform 2
- UniProtKB:	A8K4B1 (UniProtKB/TrEMBL)
- Sequence:	show sequence MASLAAANAEFCFNLFREMDDNQGNGNVFFSSLSLFAALALVRLGAQDDSLSQIDKSGLQSQLK RVFSDINASHKDYDLSIVNGLFAEKVYGFHKDYIECAEKLYDAKVERVDFTNHLEDTRRNINKW VENETHGKIKNVIGEGGISSSAVMVLVNAVYFKGKWQSAFTKSETINCHFKSPKCSGKAVAMMH QERKFNLSVIEDPSMKILELRYNGGINMYVLLPENDLSEIENKLTFQNLMEWTNPRRMTSKYVE VFFPQFKIEKNYEMKQYLRALGLKDIFDESKADLSGIASGGRLYISRMMHKSYIEVTEEGTEAT AATGSNIVEKQLPQSTLFRADHPFLFVIRKDDIILFSGKVSCP hide sequence

RefSeq Acc Id:	NP_001248759 ⟸ NM_001261830
- Peptide Label:	isoform 1
- UniProtKB:	Q1ED45 (UniProtKB/Swiss-Prot), F5GZC0 (UniProtKB/Swiss-Prot), B4DUW8 (UniProtKB/Swiss-Prot), Q3KPG4 (UniProtKB/Swiss-Prot), O75635 (UniProtKB/Swiss-Prot), A8K4B1 (UniProtKB/TrEMBL)
- Sequence:	show sequence MASLAAANAEFCFNLFREMDDNQGNGNVFFSSLSLFAALALVRLGAQDDSLSQIDKLLHVNTAS GYGNSSNSQSGLQSQLKRVFSDINASHKDYDLSIVNGLFAEKVYGFHKDYIECAEKLYDAKVER VDFTNHLEDTRRNINKWVENETHGKIKNVIGEGGISSSAVMVLVNAVYFKGKWQSAFTKSETIN CHFKSPKCSGKAVAMMHQERKFNLSVIEDPSMKILELRYNGGINMYVLLPENDLSEIENKLTFQ NLMEWTNPRRMTSKYVEVFFPQFKIEKNYEMKQYLRALGLKDIFDESKADLSGIASGGRLYISR MMHKSYIEVTEEGTEATAATGSNIVEKQLPQSTLFRADHPFLFVIRKDDIILFSGKVSCP hide sequence

RefSeq Acc Id:	XP_024307046 ⟸ XM_024451278
- Peptide Label:	isoform X1
- UniProtKB:	Q1ED45 (UniProtKB/Swiss-Prot), O75635 (UniProtKB/Swiss-Prot), F5GZC0 (UniProtKB/Swiss-Prot), B4DUW8 (UniProtKB/Swiss-Prot), Q3KPG4 (UniProtKB/Swiss-Prot), A8K4B1 (UniProtKB/TrEMBL)
- Sequence:	show sequence MASLAAANAEFCFNLFREMDDNQGNGNVFFSSLSLFAALALVRLGAQDDSLSQIDKLLHVNTAS GYGNSSNSQSGLQSQLKRVFSDINASHKDYDLSIVNGLFAEKVYGFHKDYIECAEKLYDAKVER VDFTNHLEDTRRNINKWVENETHGKIKNVIGEGGISSSAVMVLVNAVYFKGKWQSAFTKSETIN CHFKSPKCSGKAVAMMHQERKFNLSVIEDPSMKILELRYNGGINMYVLLPENDLSEIENKLTFQ NLMEWTNPRRMTSKYVEVFFPQFKIEKNYEMKQYLRALGLKDIFDESKADLSGIASGGRLYISR MMHKSYIEVTEEGTEATAATGSNIVEKQLPQSTLFRADHPFLFVIRKDDIILFSGKVSCP hide sequence

Ensembl Acc Id:

ENSP00000381101 ⟸ ENST00000398019

Ensembl Acc Id:

ENSP00000397301 ⟸ ENST00000425392

Ensembl Acc Id:

ENSP00000444861 ⟸ ENST00000546027

Ensembl Acc Id:

ENSP00000337212 ⟸ ENST00000336429

Ensembl Acc Id:

ENSP00000393947 ⟸ ENST00000431370

Ensembl Acc Id:

ENSP00000402362 ⟸ ENST00000447428

Ensembl Acc Id:

ENSP00000444572 ⟸ ENST00000540675

RefSeq Acc Id:	XP_054175265 ⟸ XM_054319290
- Peptide Label:	isoform X1
- UniProtKB:	A8K4B1 (UniProtKB/TrEMBL)

Ensembl Acc Id:

ENSP00000564216 ⟸ ENST00000894157

Ensembl Acc Id:

ENSP00000564215 ⟸ ENST00000894156

Ensembl Acc Id:

ENSP00000812049 ⟸ ENST00001132717

Protein Domains

SERPIN

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-O75635-F1-model_v2	AlphaFold	O75635	1-380	view protein structure

Promoters

RGD ID:

7237519

Promoter ID:

EPDNEW_H24504

Type:

initiation region

Name:

SERPINB7_3

Description:

serpin family B member 7

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H24505 EPDNEW_H24506

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	18	63,753,057 - 63,753,117	EPDNEW

RGD ID:

7237517

Promoter ID:

EPDNEW_H24505

Type:

initiation region

Name:

SERPINB7_1

Description:

serpin family B member 7

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H24504 EPDNEW_H24506

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	18	63,775,424 - 63,775,484	EPDNEW

RGD ID:

7237523

Promoter ID:

EPDNEW_H24506

Type:

multiple initiation site

Name:

SERPINB7_2

Description:

serpin family B member 7

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H24505 EPDNEW_H24504

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	18	63,777,781 - 63,777,841	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:13902	AgrOrtholog
COSMIC	SERPINB7	COSMIC
Ensembl Genes	ENSG00000166396	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000336429	ENTREZGENE
	ENST00000336429.6	UniProtKB/Swiss-Prot
	ENST00000398019	ENTREZGENE
	ENST00000398019.7	UniProtKB/Swiss-Prot
	ENST00000540675	ENTREZGENE
	ENST00000540675.5	UniProtKB/Swiss-Prot
	ENST00000546027	ENTREZGENE
	ENST00000546027.5	UniProtKB/Swiss-Prot
	ENST00000894156.1	UniProtKB/Swiss-Prot
	ENST00000894157	ENTREZGENE
	ENST00000894157.1	UniProtKB/Swiss-Prot
Gene3D-CATH	2.30.39.10	UniProtKB/Swiss-Prot
	3.30.497.10	UniProtKB/Swiss-Prot
GTEx	ENSG00000166396	GTEx
HGNC ID	HGNC:13902	ENTREZGENE
Human Proteome Map	SERPINB7	Human Proteome Map
InterPro	Serpin_CS	UniProtKB/Swiss-Prot
	Serpin_dom	UniProtKB/Swiss-Prot
	Serpin_fam	UniProtKB/Swiss-Prot
	Serpin_sf	UniProtKB/Swiss-Prot
	Serpin_sf_1	UniProtKB/Swiss-Prot
	Serpin_sf_2	UniProtKB/Swiss-Prot
KEGG Report	hsa:8710	UniProtKB/Swiss-Prot
NCBI Gene	8710	ENTREZGENE
OMIM	603357	OMIM
PANTHER	PTHR11461	UniProtKB/Swiss-Prot
	SERPIN B7	UniProtKB/Swiss-Prot
Pfam	Serpin	UniProtKB/Swiss-Prot
PharmGKB	PA37825	PharmGKB
PROSITE	SERPIN	UniProtKB/Swiss-Prot
SMART	SERPIN	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF56574	UniProtKB/Swiss-Prot
UniProt	A0A1B0GX82_HUMAN	UniProtKB/TrEMBL
	A8K3Q8_HUMAN	UniProtKB/TrEMBL
	A8K4B1	ENTREZGENE, UniProtKB/TrEMBL
	B4DUW8	ENTREZGENE
	C9JA68_HUMAN	UniProtKB/TrEMBL
	C9JM00_HUMAN	UniProtKB/TrEMBL
	F5GZC0	ENTREZGENE
	O75635	ENTREZGENE
	Q1ED45	ENTREZGENE
	Q3KPG4	ENTREZGENE
	SPB7_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	B4DUW8	UniProtKB/Swiss-Prot
	F5GZC0	UniProtKB/Swiss-Prot
	Q1ED45	UniProtKB/Swiss-Prot
	Q3KPG4	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-04-12	SERPINB7	serpin family B member 7		serpin peptidase inhibitor, clade B (ovalbumin), member 7	Symbol and/or name change	5135510	APPROVED

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

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