vps13a[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
nsv4681573	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 79,824,329-79,891,147 , GRCh38.p12 chr9: 77,209,413-77,276,231	VPS13A
nsv7098098	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 79,814,841-79,867,288 , GRCh38.p12 chr9: 77,199,925-77,252,372	VPS13A
nsv7098472	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 79,996,872-80,030,922 , GRCh38.p12 chr9: 77,381,956-77,416,006	VPS13A
nsv6313016	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 79,996,872-80,022,543 , GRCh38.p12 chr9: 77,381,956-77,407,627	VPS13A
nsv5673829	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 79,982,961-79,999,609 , GRCh38.p12 chr9: 77,368,045-77,384,693	VPS13A
nsv4683287	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 79,895,065-79,910,772 , GRCh38.p12 chr9: 77,280,149-77,295,856	VPS13A
nsv6313017	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 80,018,142-80,030,932 , GRCh38.p12 chr9: 77,403,226-77,416,016	VPS13A
nsv5674176	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 79,952,161-79,959,207 , GRCh38.p12 chr9: 77,337,245-77,344,291	VPS13A
nsv4683336	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 79,865,003-79,867,278 , GRCh38.p12 chr9: 77,250,087-77,252,362	VPS13A
nsv7098099	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 79,959,059-79,960,068 , GRCh38.p12 chr9: 77,344,143-77,345,152	VPS13A
nsv4683102	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 79,827,875-79,828,240 , GRCh38.p12 chr9: 77,212,959-77,213,324	VPS13A
nsv6314822	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr9: 77,246,154-77,259,082 , GRCh37.p13 chr9: 79,861,070-79,873,998	VPS13A
nsv6313015	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 79,968,430-79,969,529 , GRCh38.p12 chr9: 77,353,514-77,354,613	VPS13A
nsv7093205	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 79,929,962-79,930,333 , GRCh38 chr9: 77,315,046-77,315,417	VPS13A
nsv5674175	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 79,814,851-79,843,190 , GRCh38.p12 chr9: 77,199,935-77,228,274	VPS13A
nsv7098473	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 80,020,770-80,022,533 , GRCh38.p12 chr9: 77,405,854-77,407,617	VPS13A
nsv7097969	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 80,018,142-80,018,247 , GRCh38.p12 chr9: 77,403,226-77,403,331	VPS13A
nsv3897789	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 79,818,630-80,031,144 , GRCh38.p12 chr9: 77,203,714-77,416,228	VPS13A
nsv3909397	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 79,816,489-80,020,818 , GRCh38.p12 chr9: 77,201,573-77,405,902	VPS13A
nsv3897538	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 79,818,630-80,018,236 , GRCh38.p12 chr9: 77,203,714-77,403,320	VPS13A

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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 73

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Number of Variants: 20

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