dbVar for Gene (Select 152687) - 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
nsv7046102	inversion	1	nstd229	human		GRCh38 chr4: 87,216-92,606 , GRCh37.p13 chr4\|NW_004775427.1: 77,216-82,606 , GRCh37.p13 chr4: 87,106-92,493	ZNF595
nsv6736340	copy number variation	1	nstd229	human		GRCh38 chr4: 79,441-233,584 , GRCh37.p13 chr4\|NW_004775427.1: 69,441-223,584 , GRCh37.p13 chr4: 79,334-227,373	ZNF876P, ZNF718, 3 more genes
nsv6735015	copy number variation	1	nstd229	human		GRCh38 chr4: 73,901-82,000 , GRCh37.p13 chr4\|NW_004775427.1: 63,901-72,000 , GRCh37.p13 chr4: 73,794-81,893	ZNF595
nsv6731582	copy number variation	1	nstd229	human		GRCh38 chr4: 82,701-106,824 , GRCh37.p13 chr4\|NW_004775427.1: 72,701-96,824 , GRCh37.p13 chr4: 82,593-106,710	WEE1P1, ZNF595
nsv6726330	copy number variation	1	nstd229	human		GRCh38 chr4: 74,912-125,802 , GRCh37.p13 chr4\|NW_004775427.1: 64,912-115,802 , GRCh37.p13 chr4: 74,805-125,683	ZNF595, WEE1P1, 1 more genes
nsv6723925	copy number variation	1	nstd229	human		GRCh38 chr4: 75,998-86,103 , GRCh37.p13 chr4: 75,891-85,994 , GRCh37.p13 chr4\|NW_004775427.1: 65,998-76,103	ZNF595
nsv6719000	copy number variation	1	nstd229	human		GRCh38 chr4: 86,552-165,842 , GRCh37.p13 chr4\|NW_004775427.1: 76,552-155,842 , GRCh37.p13 chr4: 86,442-159,632	ZNF595, ZNF718, 1 more genes
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
nsv6636256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 1-12,785,001 , GRCh38.p12 chr4: 10,001-12,783,377	AFAP1-AS1, LOC389199, 294 more genes
nsv6635780	copy number variation	1	nstd227	human		GRCh38.p12 chr4: 71,674-100,039 , GRCh37 chr4: 71,566-99,926	ZNF595
nsv6634358	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344	LINC02475, LOC105374344, 658 more genes
nsv6630159	copy number variation	3	nstd224	human		GRCh37 chr4: 73,071-91,306 , GRCh38.p12 chr4: 73,179-91,419	ZNF595
nsv6630157	copy number variation	8	nstd224	human		GRCh37 chr4: 71,566-127,452 , GRCh38.p12 chr4: 71,674-133,709	ZNF595, ZNF718, 1 more genes
nsv6629982	copy number variation	1	nstd224	human		GRCh37 chr4: 73,071-124,638 , GRCh38.p12 chr4: 73,179-124,756	ZNF595, ZNF718, 1 more genes
nsv6629980	copy number variation	4	nstd224	human		GRCh37 chr4: 71,566-87,277 , GRCh38.p12 chr4: 71,674-87,387	ZNF595
nsv6629879	copy number variation	2	nstd224	human		GRCh37 chr4: 60,055-127,452 , GRCh38.p12 chr4: 60,162-133,709	ZNF718, ZNF595, 1 more genes

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Number of Variants: 20

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dbVar

Result Filters

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Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 810

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Number of Variants: 20

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