musk[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
nsv6312676	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 113,449,377-113,457,830 , GRCh38.p12 chr9: 110,687,097-110,695,550	MUSK
nsv7098418	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 113,444,934-113,449,568 , GRCh38.p12 chr9: 110,682,654-110,687,288	MUSK
nsv3883245	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 110,734,231-110,734,395 , GRCh37 chr9: 113,496,511-113,496,675	MUSK
nsv6312746	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 113,431,213-113,441,760 , GRCh38.p12 chr9: 110,668,933-110,679,480	MUSK
nsv3900038	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 113,477,528-113,480,080 , GRCh38.p12 chr9: 110,715,248-110,717,800	MUSK
nsv7098193	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 113,431,185-113,459,766 , GRCh38.p12 chr9: 110,668,905-110,697,486	MUSK
nsv7097682	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 113,509,901-113,538,955 , GRCh38.p12 chr9: 110,747,621-110,776,675	MUSK, LOC107987115
nsv5674060	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 113,496,521-113,524,498 , GRCh38.p12 chr9: 110,734,241-110,762,218	MUSK, LOC107987115
nsv3873608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 113,431,165-113,563,288 , GRCh38 chr9: 110,668,885-110,801,008	MUSK, LOC107987115, 1 more genes
nsv6312675	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 113,431,185-113,550,138 , GRCh38.p12 chr9: 110,668,905-110,787,858	MUSK, LOC107987115, 1 more genes
nsv3877943	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr9: 110,695,383-110,762,228 , GRCh37 chr9: 113,457,663-113,524,508	MUSK, RPS21P5, 1 more genes
nsv6290847	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 113,177,821-113,552,613 , GRCh38.p12 chr9: 110,415,541-110,790,333	MUSK, SVEP1, 3 more genes
nsv4675657	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 113,177,596-113,552,613 , GRCh38.p12 chr9: 110,415,316-110,790,333	MUSK, SVEP1, 3 more genes
nsv3891722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 104,604,851-126,253,089 , GRCh38.p12 chr9: 101,842,569-123,490,810	MUSK, LOC107987013, 326 more genes
nsv3917989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 102,112,198-118,529,754 , NCBI36 chr9: 101,152,019-117,569,575 , GRCh38 chr9: 99,349,916-115,767,475	MUSK, CTNNAL1, 262 more genes
nsv3922633	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 99,138,048-115,011,033 , NCBI36 chr9: 100,940,151-116,813,133 , GRCh37 chr9: 101,900,330-117,773,312	MUSK, RAD23B, 262 more genes
nsv3891066	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 113,083,182-126,779,494 , GRCh38.p12 chr9: 110,320,902-124,017,215	MUSK, FKBP15, 211 more genes
nsv3891403	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 103,271,401-113,948,226 , GRCh38.p12 chr9: 100,509,119-111,185,946	MUSK, LOC112268038, 158 more genes
nsv3911862	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 109,332,416-119,768,043 , GRCh38 chr9: 107,530,314-117,965,944 , GRCh37 chr9: 110,292,595-120,728,222	MUSK, RPL36AP6, 164 more genes
nsv3916125	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 103,767,420-112,984,794 , NCBI36 chr9: 105,569,522-114,786,895 , GRCh37 chr9: 106,529,701-115,747,074	MUSK, FRRS1L, 149 more genes

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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

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Items: 1 to 20 of 50

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Number of Variants: 20

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