polr1f[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
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	POLR1F, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	POLR1F, LOC107986817, 2014 more genes
nsv3915219	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,649,696-25,800,180 , GRCh38 chr7: 10,610,069-25,760,560 , NCBI36 chr7: 10,616,221-25,766,705	POLR1F, SNORD93, 176 more genes
nsv6313854	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 9,358,316-20,982,082 , GRCh38.p12 chr7: 9,318,686-20,942,463	POLR1F, LOC107986766, 115 more genes
nsv3911741	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 15,573,437-24,891,051 , GRCh38 chr7: 15,533,812-24,851,432 , NCBI36 chr7: 15,539,962-24,857,576	POLR1F, LINC01162, 124 more genes
nsv4674987	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 13,886,653-20,267,202 , GRCh38.p12 chr7: 13,847,028-20,227,579	POLR1F, BZW2, 64 more genes
nsv4768371	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 14,470,668-20,385,165 , GRCh38.p12 chr7: 14,431,043-20,345,542	POLR1F, HDAC9, 60 more genes
nsv3922488	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 16,161,141-20,647,522 , GRCh38 chr7: 16,121,516-20,607,899 , NCBI36 chr7: 16,127,666-20,614,047	POLR1F, HDAC9, 53 more genes
nsv3917282	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 19,145,712-22,193,713 , GRCh37 chr7: 19,185,335-22,233,331 , NCBI36 chr7: 19,151,860-22,199,856	POLR1F, MIR3146, 33 more genes
nsv3916418	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 18,505,390-21,417,733 , GRCh37 chr7: 18,545,013-21,457,351 , NCBI36 chr7: 18,511,538-21,423,876	POLR1F, FERD3L, 32 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	POLR1F, RNU6-565P, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	POLR1F, RPL23AP51, 2684 more genes
nsv3909087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620	POLR1F, MNX1-AS2, 2682 more genes
nsv3908592	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017	POLR1F, TRGV3, 2682 more genes
nsv3915802	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-41,915,483 , GRCh38 chr7: 54,185-41,875,885 , NCBI36 chr7: 149,268-41,882,008	POLR1F, RPL23AP52, 638 more genes
nsv3899194	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 11,048,840-52,863,626 , GRCh38.p12 chr7: 11,009,213-52,795,933	POLR1F, BRWD1P3, 590 more genes
nsv3918785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-37,129,317 , NCBI36 chr7: 149,268-37,095,842 , GRCh38 chr7: 54,185-37,089,712	POLR1F, MMD2, 554 more genes
nsv3903410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 704,573-29,257,946 , GRCh38.p12 chr7: 664,936-29,218,330	POLR1F, LOC100131264, 422 more genes
nsv3922329	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-27,236,023 , GRCh38 chr7: 43,360-27,196,404 , NCBI36 chr7: 138,443-27,202,548	POLR1F, LOC401312, 411 more genes
nsv3916683	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-26,867,253 , NCBI36 chr7: 149,268-26,833,778 , GRCh38 chr7: 54,185-26,827,634	POLR1F, ZNF12, 389 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 35

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Number of Variants: 20

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Search details

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