sp8[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
nsv3912031	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr7: 20,739,601-20,960,226 , GRCh38 chr7: 20,733,453-20,954,082 , GRCh37 chr7: 20,773,076-20,993,701	SP8, LINC01162, 3 more genes
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	SP8, 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	SP8, 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	SP8, 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	SP8, LOC107986766, 115 more genes
nsv3922885	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 20,561,456-32,005,143 , GRCh37 chr7: 20,601,079-32,044,755 , NCBI36 chr7: 20,567,604-32,011,280	SP8, IL6-AS1, 195 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	SP8, LINC01162, 124 more genes
nsv3916054	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 20,217,060-27,855,544 , GRCh37 chr7: 20,250,535-27,889,019 , GRCh38 chr7: 20,210,912-27,849,400	SP8, MIR148A, 139 more genes
nsv3891669	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 43,013,365-47,241,534 , GRCh38.p12 chr19: 42,509,213-46,738,277	MIR320E, BCL3, 189 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	SP8, 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	SP8, 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	SP8, 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	SP8, 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	SP8, 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	SP8, TRGV3, 2682 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	ZNF321P, ZNF861P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	BABAM1, BEST2, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	LENG8, SYDE1, 2408 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	SP8, 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	SP8, BRWD1P3, 590 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

Additional filters

Search results

Items: 1 to 20 of 50

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Number of Variants: 20

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