dbVar for Gene (Select 10296) - 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
nsv7142027	insertion	1	nstd232	human		GRCh37.p13 chr4: 1,289,489-1,289,489 , GRCh38.p12 chr4: 1,295,701-1,295,701	MAEA
nsv7140987	insertion	1	nstd232	human		GRCh37.p13 chr4: 1,313,435-1,313,435 , GRCh38.p12 chr4: 1,319,647-1,319,647	MAEA
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
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
nsv6736484	copy number variation	1	nstd229	human		GRCh38 chr4: 1,301,557-1,305,207 , GRCh37.p13 chr4: 1,295,345-1,298,995	MAEA
nsv6730554	copy number variation	1	nstd229	human		GRCh38 chr4: 1,286,014-1,845,501 , GRCh37.p13 chr4: 1,279,802-1,847,228	TMEM129, FGFR3, 12 more genes
nsv6725828	copy number variation	1	nstd229	human		GRCh38 chr4: 1,305,365-1,310,697 , GRCh37.p13 chr4: 1,299,153-1,304,485	MAEA
nsv6721057	copy number variation	1	nstd229	human		GRCh38 chr4: 1,308,729-1,310,898 , GRCh37.p13 chr4: 1,302,517-1,304,686	MAEA
nsv6719488	copy number variation	1	nstd229	human		GRCh38 chr4: 1,316,318-1,316,348 , GRCh37.p13 chr4: 1,310,106-1,310,136	MAEA
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
nsv6636534	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 963,688-2,913,553 , GRCh38.p12 chr4: 969,900-2,911,826	ADD1, CTBP1, 53 more genes
nsv6636307	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 1,180,181-2,009,278 , GRCh38.p12 chr4: 1,186,393-2,007,551	LOC105374348, SPON2, 22 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
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
nsv6372706	copy number variation	1	nstd223	human		GRCh38 chr4: 1,320,577-1,321,249 , GRCh37.p13 chr4: 1,314,365-1,315,037	MAEA
nsv6362346	copy number variation	1	nstd223	human		GRCh38 chr4: 1,320,046-1,320,612 , GRCh37.p13 chr4: 1,313,834-1,314,400	MAEA
nsv6315440	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 114,784-47,569,569 , GRCh38.p12 chr4: 114,902-47,567,552	FAM86KP, ENPP7P11, 631 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

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Study Type

Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 741

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Number of Variants: 20

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