myh8[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6314080	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 10,278,214-10,318,636 , GRCh38.p12 chr17: 10,374,897-10,415,319	MYH8, MYHAS
nsv3900889	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 10,234,834-10,299,757 , GRCh38.p12 chr17: 10,331,517-10,396,440	MYH8, MYH13, 1 more genes
nsv3898992	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 10,232,311-10,295,497 , GRCh38.p12 chr17: 10,328,994-10,392,180	MYH8, MYH13, 1 more genes
nsv4457753	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 10,233,434-10,305,820 , GRCh38.p12 chr17: 10,330,117-10,402,503	MYH8, MYH13, 1 more genes
nsv6314169	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 10,240,024-10,307,705 , GRCh38.p12 chr17: 10,336,707-10,404,388	MYH8, MYH13, 1 more genes
nsv6637414	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 10,240,025-10,307,705 , GRCh38.p12 chr17: 10,336,708-10,404,388	MYH8, MYHAS, 1 more genes
nsv4450850	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 10,233,704-10,298,758 , GRCh38 chr17: 10,330,387-10,395,441	MYH8, MYHAS, 1 more genes
nsv6291544	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 10,240,025-10,295,515 , GRCh38.p12 chr17: 10,336,708-10,392,198	MYH8, MYH13, 1 more genes
nsv4681489	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 9,698,245-10,451,247 , GRCh38.p12 chr17: 9,794,928-10,547,930	MYH8, MYH2, 11 more genes
nsv3917187	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 10,178,551-10,744,358 , GRCh37 chr17: 10,237,826-10,803,633 , GRCh38 chr17: 10,334,509-10,900,316	MYH8, MYH2, 14 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	MYH8, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	MYH8, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	MYH8, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	MYH8, SMURF2, 2366 more genes
nsv3897625	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-15,027,737 , GRCh38.p12 chr17: 150,732-15,124,420	MYH8, GP1BA, 439 more genes
nsv3915354	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519	MYH8, KIF1C-AS1, 433 more genes
nsv3917059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901	MYH8, PSMB6, 409 more genes
nsv7148254	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413	MYH8, RFLNB, 401 more genes
nsv3904771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-11,186,432 , GRCh38.p12 chr17: 150,732-11,283,115	MYH8, SLC2A4, 401 more genes
nsv3911050	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 5,732,953-12,095,349 , GRCh37 chr17: 5,636,273-11,998,666 , NCBI36 chr17: 5,576,997-11,939,391	MYH8, C17orf49, 209 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 33

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Number of Variants: 20

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Supplemental Content

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Search details

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