cpa3[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
nsv3883171	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 148,533,396-148,610,084 , GRCh38.p12 chr3: 148,815,609-148,892,297	CPA3, HMGB1P30, 1 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	RNU6-438P, LOC105375300, 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	LOC107986817, DNAJB9, 2014 more genes
nsv6290244	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334	CPA3, LOC102724145, 273 more genes
nsv3916726	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 116,754,095-134,125,980 , GRCh38 chr7: 117,326,805-134,790,689 , GRCh37 chr7: 116,966,859-134,475,440	LOC107986845, TPI1P2, 245 more genes
nsv3920790	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 134,257,180-149,729,538 , NCBI36 chr3: 135,458,712-150,930,015 , GRCh37 chr3: 133,976,022-149,447,325	CPA3, TFDP2, 203 more genes
nsv3903275	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 127,295,698-139,524,358 , GRCh38.p12 chr7: 127,655,644-139,824,559	RNU6-1272P, KCP, 224 more genes
nsv6313876	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 124,103,982-134,693,590 , GRCh38.p12 chr7: 124,463,928-135,008,839	IMPDH1, SSU72L6, 174 more genes
nsv3910648	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 124,170,657-134,163,594 , GRCh37 chr7: 123,810,711-133,848,346 , NCBI36 chr7: 123,597,947-133,498,886	CPA1, ARF5, 165 more genes
nsv6313722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 123,967,475-132,729,981 , GRCh38.p12 chr7: 124,327,421-133,045,221	IRF5, MIR129-1, 153 more genes
nsv3915522	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 126,859,732-132,750,936 , NCBI36 chr7: 126,287,022-132,086,236 , GRCh37 chr7: 126,499,786-132,435,696	LRRC4, LINC-PINT, 126 more genes
nsv3887637	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 148,425,748-153,220,169 , GRCh38.p12 chr3: 148,707,961-153,502,380	CPA3, LOC101927942, 97 more genes
nsv6311444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 148,447,967-151,176,497 , GRCh38.p12 chr3: 148,730,180-151,458,709	CPA3, TM4SF1, 68 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	CPA3, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	CPA3, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	CPA3, RPL23AP49, 2875 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	RNU6-565P, LAMB1, 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	RPL23AP51, FLJ40288, 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	MNX1-AS2, VN1R31P, 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	TRGV3, SNX10-AS1, 2682 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 46

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Number of Variants: 20

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