dbVar for Gene (Select 3425) - 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
nsv7148161	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194	SLIRPP2, STIM2-AS1, 659 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	OR7E84P, FAM193A, 764 more genes
nsv7137196	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072	ECM1P2, LOC105378240, 482 more genes
nsv7136956	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 996,520-998,294 , GRCh37 chr4: 990,308-992,082	IDUA
nsv7097251	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 493,125-1,843,544 , GRCh38.p12 chr4: 499,336-1,841,817	PDE6B, LOC105374339, 44 more genes
nsv7097011	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 980,871-981,050 , GRCh38.p12 chr4: 987,083-987,262	IDUA, SLC26A1
nsv7097010	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 980,775-981,040 , GRCh38.p12 chr4: 986,987-987,252	SLC26A1, IDUA
nsv7096869	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 980,871-985,491 , GRCh38.p12 chr4: 987,083-991,703	IDUA, SLC26A1
nsv7096733	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 520,808-1,020,391 , GRCh38.p12 chr4: 527,019-1,026,603	PDE6B-AS1, PIGG, 19 more genes
nsv7056080	inversion	1	nstd229	human		GRCh38 chr4: 802,364-1,026,131 , GRCh37.p13 chr4: 796,152-1,019,919	LOC105374341, LOC105374340, 7 more genes
nsv6737732	copy number variation	1	nstd229	human		GRCh38 chr4: 963,501-1,026,300 , GRCh37.p13 chr4: 957,289-1,020,088	DGKQ, SLC26A1, 2 more genes
nsv6733867	copy number variation	1	nstd229	human		GRCh38 chr4: 997,141-997,284 , GRCh37.p13 chr4: 990,929-991,072	IDUA
nsv6730128	copy number variation	1	nstd229	human		GRCh38 chr4: 813,467-1,049,563 , GRCh37.p13 chr4: 807,255-1,043,351	TMEM175, LOC105374341, 8 more genes
nsv6729814	copy number variation	1	nstd229	human		GRCh38 chr4: 932,438-1,207,526 , GRCh37.p13 chr4: 926,226-1,201,314	SPON2, LOC100421802, 11 more genes
nsv6728558	copy number variation	1	nstd229	human		GRCh38 chr4: 852,148-1,011,710 , GRCh37.p13 chr4: 845,936-1,005,498	LOC105374341, IDUA, 5 more genes
nsv6728138	copy number variation	1	nstd229	human		GRCh38 chr4: 989,419-992,714 , GRCh37.p13 chr4: 983,207-986,502	IDUA, SLC26A1
nsv6727583	copy number variation	1	nstd229	human		GRCh38 chr4: 988,538-994,222 , GRCh37.p13 chr4: 982,326-988,010	IDUA, SLC26A1
nsv6725712	copy number variation	1	nstd229	human		GRCh38 chr4: 988,301-990,200 , GRCh37.p13 chr4: 982,089-983,988	IDUA, SLC26A1
nsv6636691	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-2,437,290 , GRCh38.p12 chr4: 68,454-2,435,563	SPON2, TACC3, 77 more genes
nsv6636582	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-12,369,983 , GRCh38.p12 chr4: 68,454-12,368,359	NELFA, OR7E111FP, 289 more genes

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Number of Variants: 20

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Organism

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Has Clinical Interpretation

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Items: 1 to 20 of 633

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Number of Variants: 20

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