dbVar for Gene (Select 56922) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7145298	insertion	1	nstd232	human		GRCh37.p13 chr3: 182,735,607-182,735,607 , GRCh38.p12 chr3: 183,017,819-183,017,819	MCCC1
nsv7098855	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,759,355-182,759,538 , GRCh38.p12 chr3: 183,041,567-183,041,750	MCCC1
nsv7096950	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,754,986-182,775,230 , GRCh38.p12 chr3: 183,037,198-183,057,442	MCCC1
nsv7096554	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,754,986-182,770,048 , GRCh38.p12 chr3: 183,037,198-183,052,260	MCCC1
nsv7096553	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr3: 182,733,226-184,094,097 , GRCh38.p12 chr3: 183,015,438-184,376,309	DVL3, LOC105374247, 51 more genes
nsv7096453	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,769,927-182,817,228 , GRCh38.p12 chr3: 183,052,139-183,099,440	MCCC1
nsv7096452	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,756,794-182,763,348 , GRCh38.p12 chr3: 183,039,006-183,045,560	MCCC1
nsv7093524	insertion	1	nstd102	human	Uncertain significance	GRCh37 chr3: 182,788,979-182,788,979 , GRCh38 chr3: 183,071,191-183,071,191	MCCC1
nsv7042683	inversion	1	nstd229	human		GRCh38 chr3: 183,046,548-183,109,310 , GRCh37.p13 chr3: 182,764,336-182,827,098	MCCC1, LOC105374247
nsv6737608	copy number variation	1	nstd229	human		GRCh38 chr3: 183,087,603-183,096,090 , GRCh37.p13 chr3: 182,805,391-182,813,878	MCCC1
nsv6734120	copy number variation	1	nstd229	human		GRCh38 chr3: 182,627,709-183,043,122 , GRCh37.p13 chr3: 182,345,497-182,760,910	MCCC1, ATP11B, 7 more genes
nsv6733993	copy number variation	1	nstd229	human		GRCh38 chr3: 183,026,268-183,056,902 , GRCh37.p13 chr3: 182,744,056-182,774,690	MCCC1
nsv6733547	copy number variation	1	nstd229	human		GRCh38 chr3: 183,062,789-183,068,278 , GRCh37.p13 chr3: 182,780,577-182,786,066	MCCC1
nsv6732087	copy number variation	1	nstd229	human		GRCh38 chr3: 183,064,146-183,064,238 , GRCh37.p13 chr3: 182,781,934-182,782,026	MCCC1
nsv6729489	copy number variation	1	nstd229	human		GRCh38 chr3: 183,087,001-183,119,900 , GRCh37.p13 chr3: 182,804,789-182,837,688	MCCC1, LOC105374247
nsv6728983	copy number variation	1	nstd229	human		GRCh38 chr3: 183,084,601-183,121,800 , GRCh37.p13 chr3: 182,802,389-182,839,588	MCCC1, LOC105374247, 1 more genes
nsv6724499	copy number variation	1	nstd229	human		GRCh38 chr3: 183,057,859-183,067,371 , GRCh37.p13 chr3: 182,775,647-182,785,159	MCCC1
nsv6635458	copy number variation	1	nstd227	human		GRCh37 chr3: 182,754,967-182,778,941 , GRCh38.p12 chr3: 183,037,179-183,061,153	MCCC1
nsv6634384	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 181,062,175-185,474,509 , GRCh38.p12 chr3: 181,344,387-185,756,721	PRICKLE1P1, KLHL24, 99 more genes
nsv6634371	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559	ACTL6A, AHSG, 466 more genes

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

Send to:

Links from Gene

Items: 1 to 20 of 334

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Recent activity

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 334

Page of 17

Number of Variants: 20

Page of 17

Supplemental Content

Find related data

Recent activity