spast[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
nsv3878938	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 32,063,812-32,154,516 , GRCh37.p13 chr2: 32,288,881-32,379,585	SPAST
nsv4681594	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 32,288,891-32,379,575 , GRCh38.p12 chr2: 32,063,822-32,154,506	SPAST
nsv6311667	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,288,901-32,379,565 , GRCh38.p12 chr2: 32,063,832-32,154,496	SPAST
nsv5673698	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,288,901-32,366,973 , GRCh38.p12 chr2: 32,063,832-32,141,904	SPAST
nsv1398362	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,291,802-32,364,656 , GRCh38 chr2: 32,066,734-32,139,588	SPAST
nsv1398605	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,291,779-32,357,195 , GRCh38 chr2: 32,066,710-32,132,126	SPAST
nsv6636019	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,314,684-32,379,575 , GRCh38.p12 chr2: 32,089,615-32,154,506	SPAST
nsv1398019	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 32,083,472-32,142,854 , GRCh37 chr2: 32,308,541-32,367,923	SPAST
nsv5673359	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,323,961-32,379,442 , GRCh38.p12 chr2: 32,098,892-32,154,373	SPAST
nsv3888233	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 32,063,812-32,116,232 , GRCh37.p13 chr2: 32,288,881-32,341,301	SPAST
nsv7096634	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,288,901-32,341,301 , GRCh38.p12 chr2: 32,063,832-32,116,232	SPAST
nsv5673536	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,288,891-32,341,291 , GRCh38.p12 chr2: 32,063,822-32,116,222	SPAST
nsv1398234	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,302,137-32,351,058 , GRCh38 chr2: 32,077,068-32,125,989	SPAST
nsv6636079	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,314,684-32,361,622 , GRCh38.p12 chr2: 32,089,615-32,136,553	SPAST
nsv1398466	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,329,723-32,373,142 , GRCh38 chr2: 32,104,654-32,148,073	SPAST
nsv3886067	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 32,114,638-32,157,637 , GRCh37 chr2: 32,339,707-32,382,706	SPAST
nsv7096501	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,339,687-32,379,565 , GRCh38.p12 chr2: 32,114,618-32,154,496	SPAST
nsv5673699	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,339,697-32,379,575 , GRCh38.p12 chr2: 32,114,628-32,154,506	SPAST
nsv5673360	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,341,281-32,379,565 , GRCh38.p12 chr2: 32,116,212-32,154,496	SPAST
nsv5673199	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,341,282-32,379,442 , GRCh38.p12 chr2: 32,116,213-32,154,373	SPAST

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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 166

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Number of Variants: 20

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