Product Details

System Message

See other MYH7B CNV Assays ›

Gene Symbol: MYH7B
Assay Reference Genome Location: Chr.20:34998271 on build GRCh38
Cytoband: 20q11.22

Assay ID

Hs02681408_cn

Size

Availability	Made To Order
Catalog #	4400291
Price (USD)	457.00
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Genomic Map
Assay Details
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Genomic Map

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Assay Details

Target Gene Details

Entrez Gene ID:	57644
Gene Name:	myosin heavy chain 7B
Gene Aliases:	MHC14, MYH14
Location:	Chr.20:34955835-35002437 on Build GRCh38
Assay Gene Location:	Overlaps Intron 34 - Exon 35

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
MYH7B	NM_020884.4			NP_065935.3
	XM_006723840.3			XP_006723903.1
	XM_011528941.2			XP_011527243.1
	XM_011528947.2			XP_011527249.1
	XM_011528948.2			XP_011527250.1
	XM_017027986.1			XP_016883475.1
	XM_017027987.1			XP_016883476.1
	AB040945.2
	BC007808.1			AAH07808.1
	BC151242.1

Target Copy Number Variation Details

DGV Version:

Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv1063673	Chr.20:34977862 - 35009073 on Build GRCh38	Loss	MIR499B MIR499A MYH7B TRPC4AP
nsv1055447	Chr.20:34737641 - 35020344 on Build GRCh38	Loss	MIR499B MIR499A GSS HMGB3P1 MYH7B TRPC4AP GGT7 NCOA6 ACSS2
nsv833962	Chr.20:34927688 - 35113250 on Build GRCh38	Loss	MIR499B MIR499A GSS MYH7B TRPC4AP ACSS2
nsv3362	Chr.20:34978502 - 35010725 on Build GRCh38	Insertion	MIR499B MIR499A MYH7B TRPC4AP

More Information

Set Membership:

Intragenic

Non-exonic

DGV Variation

Gene Ontology Categories:

Process(es)

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