adgra3[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
nsv4674471	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 22,351,408-22,429,851 , GRCh38.p12 chr4: 22,349,785-22,428,228	ADGRA3
nsv6311723	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 22,389,328-22,425,995 , GRCh38.p12 chr4: 22,387,705-22,424,372	ADGRA3
nsv6312248	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 22,517,131-22,517,407 , GRCh38.p12 chr4: 22,515,508-22,515,784	ADGRA3, MIR12115
nsv3877950	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 4,165,334-33,324,781 , GRCh38.p12 chr4: 4,163,607-33,323,159	ADGRA3, LOC100418700, 353 more genes
nsv3885762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 71,552-29,006,745 , GRCh38.p12 chr4: 71,660-29,005,123	ADGRA3, CD38, 456 more genes
nsv3923296	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 72,555-28,066,309 , NCBI36 chr4: 62,447-27,677,029 , GRCh37 chr4: 72,447-28,067,931	ADGRA3, OR7E99P, 446 more genes
nsv7098818	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 11,399,082-38,137,335 , GRCh37.p13 chr4: 11,400,706-38,138,956	ADGRA3, LOC105374542, 232 more genes
nsv4674378	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-24,280,482 , GRCh38.p12 chr4: 49,556-24,278,859	ADGRA3, USP17L30, 394 more genes
nsv6313559	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 19,892,850-37,325,128 , GRCh38.p12 chr4: 19,891,227-37,323,506	ADGRA3, LOC102723846, 135 more genes
nsv3911497	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 16,925,022-32,113,076 , NCBI36 chr4: 16,535,743-31,758,596 , GRCh37 chr4: 16,926,645-32,114,698	ADGRA3, LINC02506, 128 more genes
nsv4347528	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,778,849-27,760,141 , GRCh38.p12 chr4: 12,777,225-27,758,519	ADGRA3, MTCO3P44, 148 more genes
nsv4674448	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 20,406,475-29,134,345 , GRCh38.p12 chr4: 20,404,852-29,132,723	ADGRA3, LOC100288962, 84 more genes
nsv4347791	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 19,186,845-24,548,281 , GRCh38.p12 chr4: 19,185,222-24,546,658	ADGRA3, PACRGL, 29 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	ADGRA3, 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	ADGRA3, 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	ADGRA3, 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	ADGRA3, 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	ADGRA3, 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	ADGRA3, 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	ADGRA3, OR7E84P, 764 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 43

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Number of Variants: 20

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Supplemental Content

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