dbVar for Gene (Select 104502417) - 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
nsv5538918	copy number variation	1	nstd206	human		GRCh38 chr22: 39,472,667-39,476,096 , GRCh37.p13 chr22: 39,868,672-39,872,101	MGAT3, MGAT3-AS1
nsv5288097	copy number variation	1	nstd204	human		GRCh38.p13 chr22: 38,982,101-39,534,900 , GRCh37.p13 chr22: 39,378,106-39,930,905	APOBEC3C, COX5BP7, 25 more genes
nsv5032147	copy number variation	1	nstd200	human		GRCh38 chr22: 39,472,667-39,476,096 , GRCh37.p13 chr22: 39,868,672-39,872,101	MGAT3-AS1, MGAT3
nsv4729926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824	FBXO7, GTSE1, 1084 more genes
nsv4676292	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410	PDXP-DT, PDGFB, 550 more genes
nsv4457771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410	IGLV3-27, XKR3, 1082 more genes
nsv3923309	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr22: 37,873,393-39,965,372 , GRCh37.p13 chr22: 39,543,447-41,635,426 , GRCh38.p12 chr22: 39,147,442-41,239,422	MIR1281, CBX7, 57 more genes
nsv3922654	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 37,721,797-40,860,953 , GRCh37 chr22: 38,117,804-41,256,957 , NCBI36 chr22: 36,447,750-39,586,903	RPS29P31, UQCRFS1P1, 103 more genes
nsv3919881	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 17,397,633-51,178,213 , GRCh38 chr22: 16,916,743-50,739,785 , NCBI36 chr22: 15,777,633-49,525,079	MIR12114, MIR6820, 1059 more genes
nsv3919085	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 17,008,132-49,591,432 , GRCh37.p13 chr22: 18,628,132-51,244,566 , GRCh38.p12 chr22: 18,145,365-50,806,138	IGLV2-28, LINC01310, 1023 more genes
nsv3913775	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 15,777,498-49,525,130 , GRCh38 chr22: 16,916,608-50,739,836 , GRCh37 chr22: 17,397,498-51,178,264	ZNF280A, RFPL1S, 1059 more genes
nsv3910659	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 37,642,438-49,574,364 , GRCh37.p13 chr22: 39,312,492-51,227,498 , GRCh38.p12 chr22: 38,916,487-50,789,070	LOC100506472, MCHR1, 314 more genes
nsv3910634	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 37,061,769-50,738,932 , NCBI36 chr22: 35,787,755-49,524,226 , GRCh37 chr22: 37,457,809-51,177,360	HDAC10, RPS25P10, 381 more genes
nsv3907231	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,114,244-51,211,392 , GRCh38.p12 chr22: 16,367,190-50,772,964	DDTL, PPP1R26P3, 1084 more genes
nsv3906962	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 35,728,929-51,220,961 , GRCh38.p12 chr22: 35,332,936-50,782,533	UQCRFS1P1, APOBEC3F, 435 more genes
nsv3902776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,667-51,243,435 , GRCh38.p12 chr22: 16,367,190-50,805,007	LOC100419811, MTCO2P20, 1084 more genes
nsv3902598	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,220,902 , GRCh38.p12 chr22: 16,367,190-50,782,474	FABP5P11, SLC2A11, 1084 more genes
nsv3894026	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,237,518 , GRCh38.p12 chr22: 16,367,190-50,799,090	IGKV3OR22-2, ZDHHC8, 1084 more genes
nsv3891895	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,900-51,197,838 , GRCh38.p12 chr22: 16,408,174-50,759,410	POM121L7P, RPS10P31, 1082 more genes
nsv3890411	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,237,463 , GRCh38.p12 chr22: 16,367,190-50,799,035	RNU6-495P, KIAA1656, 1084 more genes

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Number of Variants: 20

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