dbVar for Gene (Select 146664) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6130285	insertion	1	nstd186	human		GRCh37 chr17: 74,912,142-74,912,168 , GRCh38.p12 chr17: 76,916,060-76,916,086	MGAT5B
nsv5936965	copy number variation	1	nstd209	human		GRCh38 chr17: 76,916,110-76,916,202 , GRCh37.p13 chr17: 74,912,192-74,912,284	MGAT5B
nsv5658431	insertion	2	nstd207	human		GRCh38 chr17: 76,925,235-76,925,235 , GRCh37.p13 chr17: 74,921,317-74,921,317	MGAT5B
nsv5655842	insertion	1	nstd207	human		GRCh38 chr17: 76,916,110-76,916,110 , GRCh37.p13 chr17: 74,912,192-74,912,192	MGAT5B
nsv5550817	insertion	1	nstd206	human		GRCh38 chr17: 76,916,060-76,916,086 , GRCh37.p13 chr17: 74,912,142-74,912,168	MGAT5B
nsv5539581	insertion	1	nstd206	human		GRCh38 chr17: 76,925,254-76,925,286 , GRCh37.p13 chr17: 74,921,336-74,921,368	MGAT5B
nsv5530835	copy number variation	1	nstd206	human		GRCh38 chr17: 76,914,518-76,915,072 , GRCh37.p13 chr17: 74,910,600-74,911,154	MGAT5B
nsv5527649	copy number variation	1	nstd206	human		GRCh38 chr17: 76,931,687-76,932,579 , GRCh37.p13 chr17: 74,927,769-74,928,661	MGAT5B
nsv5349684	translocation	1	nstd200	human		GRCh38 chr17: 76,932,579-76,932,579 , GRCh38 chr17: 76,931,687-76,931,687 , GRCh37.p13 chr17: 74,927,769-74,927,769 , GRCh37.p13 chr17: 74,928,661-74,928,661	MGAT5B
nsv5183602	mobile element insertion	1	nstd203	human		GRCh38 chr17: 76,928,280-76,928,296 , GRCh37.p13 chr17: 74,924,362-74,924,378	MGAT5B
nsv5016788	copy number variation	1	nstd200	human		GRCh38 chr17: 76,919,125-76,919,199 , GRCh37.p13 chr17: 74,915,207-74,915,281	MGAT5B
nsv5016787	copy number variation	1	nstd200	human		GRCh38 chr17: 76,908,386-76,913,433 , GRCh37.p13 chr17: 74,904,468-74,909,515	MGAT5B
nsv5014043	copy number variation	1	nstd200	human		GRCh38 chr17: 76,942,347-76,970,727 , GRCh37.p13 chr17: 74,938,429-74,966,809	LOC105371899, MGAT5B
nsv4859056	copy number variation	1	nstd200	human		GRCh37 chr17: 74,927,769-74,928,661 , GRCh38.p12 chr17: 76,931,687-76,932,579	MGAT5B
nsv4854405	copy number variation	1	nstd200	human		GRCh37 chr17: 74,938,429-74,966,809 , GRCh38.p12 chr17: 76,942,347-76,970,727	LOC105371899, MGAT5B
nsv4754191	insertion	1	nstd199	human		GRCh37 chr17: 74,921,307-74,921,307 , GRCh38.p12 chr17: 76,925,225-76,925,225	MGAT5B
nsv4676341	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 74,509,193-75,602,123 , GRCh38.p12 chr17: 76,513,111-77,606,041	CYCSP40, RNU6-97P, 38 more genes
nsv4676104	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963	LLGL2, TSEN54, 165 more genes
nsv4633511	copy number variation	1	nstd183	human		GRCh37 chr17: 74,851,635-74,886,477 , GRCh38.p12 chr17: 76,855,553-76,890,395	LINC00868, MGAT5B
nsv4632857	copy number variation	1	nstd183	human		GRCh37 chr17: 74,850,620-74,886,137 , GRCh38.p12 chr17: 76,854,538-76,890,055	MGAT5B, LINC00868

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 301

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 301

Page of 16

Number of Variants: 20

Page of 16

Supplemental Content

Find related data

Recent activity