cnga1[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
nsv6311834	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 47,938,438-47,945,449 , GRCh38.p12 chr4: 47,936,421-47,943,432	CNGA1, LOC101927157
nsv4681255	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 47,938,438-47,945,429 , GRCh38.p12 chr4: 47,936,421-47,943,412	CNGA1, LOC101927157
nsv6312252	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr4: 47,938,438-47,954,718 , GRCh38.p12 chr4: 47,936,421-47,952,701	CNGA1, LOC101927157
nsv6312253	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 47,945,178-47,945,449 , GRCh38.p12 chr4: 47,943,161-47,943,432	CNGA1, LOC101927157
nsv4683103	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 47,945,198-47,945,429 , GRCh38.p12 chr4: 47,943,181-47,943,412	CNGA1, LOC101927157
nsv3872610	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 47,936,543-48,036,737 , GRCh38.p12 chr4: 47,934,526-48,034,720	CNGA1, LOC101927157, 1 more genes
nsv4674279	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 47,913,550-48,036,790 , GRCh38.p12 chr4: 47,911,533-48,034,773	CNGA1, NFXL1, 2 more genes
nsv4456981	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 47,923,830-48,067,957 , GRCh38.p12 chr4: 47,921,813-48,065,940	CNGA1, NIPAL1, 2 more genes
nsv4456423	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 47,923,813-48,053,663 , GRCh38.p12 chr4: 47,921,796-48,051,646	CNGA1, NIPAL1, 1 more genes
nsv4455540	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 47,923,831-48,053,007 , GRCh38.p12 chr4: 47,921,814-48,050,990	CNGA1, NIPAL1, 1 more genes
nsv4681677	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 47,938,438-48,032,193 , GRCh38.p12 chr4: 47,936,421-48,030,176	CNGA1, LOC101927157, 1 more genes
nsv3873978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724	CNGA1, LOC100422029, 2358 more genes
nsv3876533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611	CNGA1, LOC100420289, 2347 more genes
nsv3884499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286	CNGA1, MTND4LP29, 2341 more genes
nsv3880085	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318	CNGA1, LOC112268460, 2345 more genes
nsv3883791	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495	CNGA1, LOC105377343, 2341 more genes
nsv3872797	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-66,440,622 , GRCh38.p12 chr4: 68,453-65,574,904	CNGA1, GNPDA2, 813 more genes
nsv7148157	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396	CNGA1, OR7E84P, 764 more genes
nsv4684161	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-49,620,898 , GRCh38.p12 chr4: 49,556-49,618,881	CNGA1, TLR10, 669 more genes
nsv7148161	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194	CNGA1, SLIRPP2, 659 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 32

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Number of Variants: 20

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Supplemental Content

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