dbVar for Gene (Select 8786) - 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
nsv7094666	copy number variation	3	nstd102	human	Uncertain significance	GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571	DNAAF8, TMEM204, 282 more genes
nsv7094665	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 256,302-1,918,176 , GRCh38.p12 chr16: 206,303-1,868,175	MRPS34, LOC105371044, 97 more genes
nsv7094664	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 256,302-1,843,653 , GRCh38.p12 chr16: 206,303-1,793,652	NME4, UNKL, 94 more genes
nsv7094663	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 256,302-1,657,267 , GRCh38.p12 chr16: 206,303-1,607,266	TPSP2, PRR25, 83 more genes
nsv7094577	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 289,853-626,274 , GRCh38.p12 chr16: 239,854-576,274	ARHGDIG, DECR2, 17 more genes
nsv7094575	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 256,302-633,035 , GRCh38.p12 chr16: 206,303-583,035	FAM234A, RPL23AP5, 19 more genes
nsv6977199	copy number variation	1	nstd229	human		GRCh38 chr16: 274,895-275,061 , GRCh37.p13 chr16: 324,895-325,061	RGS11
nsv6975390	copy number variation	1	nstd229	human		GRCh38 chr16: 267,621-267,737 , GRCh37.p13 chr16: 317,620-317,736	FAM234A, RGS11
nsv6973295	copy number variation	1	nstd229	human		GRCh38 chr16: 266,856-266,927 , GRCh37.p13 chr16: 316,855-316,926	FAM234A, RGS11
nsv6972752	copy number variation	1	nstd229	human		GRCh38 chr16: 269,466-271,263 , GRCh37.p13 chr16: 319,465-321,262	FAM234A, RGS11
nsv6970909	copy number variation	1	nstd229	human		GRCh38 chr16: 269,489-275,381 , GRCh37.p13 chr16: 319,488-325,381	RGS11, FAM234A
nsv6967815	copy number variation	1	nstd229	human		GRCh38 chr16: 251,401-267,300 , GRCh37.p13 chr16: 301,400-317,299	RGS11, FAM234A
nsv6965205	copy number variation	1	nstd229	human		GRCh38 chr16: 275,301-282,200 , GRCh37.p13 chr16: 325,301-332,200	PDIA2, ARHGDIG, 1 more genes
nsv6962097	copy number variation	1	nstd229	human		GRCh38 chr16: 122,985-378,594 , GRCh37.p13 chr16: 172,984-428,594	MRPL28, HBA1, 16 more genes
nsv6960373	copy number variation	1	nstd229	human		GRCh38 chr16: 269,998-270,040 , GRCh37.p13 chr16: 319,997-320,039	FAM234A, RGS11
nsv6960265	copy number variation	1	nstd229	human		GRCh38 chr16: 159,223-287,986 , GRCh37.p13 chr16: 209,222-337,986	LUC7L, ARHGDIG, 12 more genes
nsv6959668	copy number variation	1	nstd229	human		GRCh38 chr16: 237,437-303,730 , GRCh37.p13 chr16: 287,436-353,730	FAM234A, AXIN1, 3 more genes
nsv6958164	copy number variation	1	nstd229	human		GRCh38 chr16: 270,771-282,519 , GRCh37.p13 chr16: 320,770-332,519	PDIA2, ARHGDIG, 1 more genes
nsv6637972	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-1,350,186 , GRCh38.p12 chr16: 35,881-1,300,185	MPG, LOC105371038, 78 more genes
nsv6634427	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458	HBA1, ANTKMT, 312 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

Links from Gene

Items: 1 to 20 of 349

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Number of Variants: 20

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