pum3[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
nsv3898625	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 2,804,393-2,837,218 , GRCh38.p12 chr9: 2,804,393-2,837,218	PUM3
nsv6637550	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 2,683,132-2,847,102 , GRCh38.p12 chr9: 2,683,132-2,847,102	PUM3, KCNV2
nsv3890749	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr9: 2,689,263-3,073,977 , GRCh38.p12 chr9: 2,689,263-3,073,977	PUM3, CARM1P1, 3 more genes
nsv6313769	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 2,630,683-2,841,614 , GRCh38.p12 chr9: 2,630,683-2,841,614	PUM3, KCNV2, 2 more genes
nsv4675206	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 2,582,103-2,828,969 , GRCh38.p12 chr9: 2,582,103-2,828,969	PUM3, KCNV2, 3 more genes
nsv3920950	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 194,104-18,872,279 , GRCh37 chr9: 204,104-18,882,279 , GRCh38 chr9: 204,104-18,882,281	PUM3, RPL4P5, 193 more genes
nsv3910019	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 220,253-18,708,805 , NCBI36 chr9: 210,253-18,698,803 , GRCh37 chr9: 220,253-18,708,803	PUM3, LOC107987049, 191 more genes
nsv5381767	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814	PUM3, ACTG1P14, 191 more genes
nsv4768366	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,193-18,073,357 , GRCh38.p12 chr9: 204,193-18,073,359	PUM3, DOCK8-AS1, 186 more genes
nsv3910119	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-18,063,357 , GRCh38 chr9: 204,193-18,073,359 , GRCh37 chr9: 204,193-18,073,357	PUM3, RNA5SP279, 186 more genes
nsv3917303	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 220,253-18,073,359 , GRCh37 chr9: 220,253-18,073,357 , NCBI36 chr9: 210,253-18,063,357	PUM3, DMAC1, 185 more genes
nsv4674929	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-17,789,410 , GRCh38.p12 chr9: 203,861-17,789,412	PUM3, LINC02851, 184 more genes
nsv3905168	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-17,655,298 , GRCh38.p12 chr9: 203,861-17,655,300	PUM3, RANBP6, 184 more genes
nsv3899178	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 213,161-17,496,750 , GRCh38.p12 chr9: 213,161-17,496,752	PUM3, GLIS3, 181 more genes
nsv3903505	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-17,125,893 , GRCh38.p12 chr9: 203,861-17,125,895	PUM3, RPS26P3, 179 more genes
nsv3923785	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-16,887,578 , GRCh37 chr9: 204,193-16,897,578 , GRCh38 chr9: 204,193-16,897,580	PUM3, FTH1P12, 176 more genes
nsv3890932	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-16,856,907 , GRCh38.p12 chr9: 203,861-16,856,909	PUM3, ACTG1P14, 176 more genes
nsv3917732	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 214,367-16,307,944 , GRCh37 chr9: 214,367-16,307,942 , NCBI36 chr9: 204,367-16,297,942	PUM3, RLN1, 173 more genes
nsv3919683	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 322,690-16,401,656 , NCBI36 chr9: 312,690-16,391,654 , GRCh37 chr9: 322,690-16,401,654	PUM3, DMRT2, 172 more genes
nsv3918828	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,090-15,260,598 , NCBI36 chr9: 194,090-15,250,598 , GRCh38 chr9: 204,090-15,260,600	PUM3, HMGN2P31, 160 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 181

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Number of Variants: 20

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