dbVar for Gene (Select 8220) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7148280	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 18,985,739-21,081,116 , GRCh37.p13 chr22: 18,973,252-21,435,405	SLC9A3P2, RNU6-225P, 99 more genes
nsv7148270	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,893,838-20,508,931 , GRCh38.p12 chr22: 18,483,514-20,345,217	DGCR2, MIR4761, 79 more genes
nsv7148246	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 18,893,838-21,416,074 , GRCh38.p12 chr22: 18,339,130-21,061,785	ZDHHC8, FAM230E, 121 more genes
nsv7148214	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 20,609,932-21,576,553 , GRCh38.p12 chr22: 18,339,630-21,222,264	IGLL4P, LOC107985584, 129 more genes
nsv7148166	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,893,838-20,307,561 , GRCh38.p12 chr22: 18,906,325-20,320,038	MIR6816, PRODH, 61 more genes
nsv7137215	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,916,842-20,311,810 , GRCh38.p12 chr22: 18,929,329-20,324,287	TSSK1A, ESS2, 60 more genes
nsv7137150	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,893,888-21,481,925 , GRCh38.p12 chr22: 18,339,130-21,127,636	LOC107985584, LINC00896, 125 more genes
nsv7098862	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 18,206,749-21,234,326 , GRCh37.p13 chr22: 18,689,516-21,588,615	GP1BB, IGLL4P, 132 more genes
nsv7098756	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,893,886-21,386,103 , GRCh38.p12 chr22: 18,339,130-21,031,814	CCDC188, MED15, 118 more genes
nsv7095928	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 17,565,982-20,052,185 , GRCh38.p12 chr22: 17,085,092-20,064,662	CA15P1, BID, 103 more genes
nsv7093409	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,893,888-21,570,386 , GRCh38.p12 chr22: 18,339,130-21,216,097	FAM247A, P2RX6P, 129 more genes
nsv7093403	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 19,184,000-21,416,024 , GRCh38.p12 chr22: 18,339,130-21,061,735	LOC105372862, RPL7AP70, 121 more genes
nsv7093402	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,894,078-21,414,817 , GRCh38.p12 chr22: 18,339,130-21,060,528	LOC100420103, P2RX6P, 121 more genes
nsv7093382	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,834,445-21,414,817 , GRCh38.p12 chr22: 18,339,130-21,060,528	DGCR8, SEPTIN5, 121 more genes
nsv7075430	inversion	1	nstd229	human		GRCh38 chr22: 18,971,418-20,267,248 , GRCh37.p13 chr22: 18,958,931-20,254,771	LINC00896, LOC105372861, 57 more genes
nsv7033860	copy number variation	1	nstd229	human		GRCh38 chr22: 19,052,570-19,211,240 , GRCh37.p13 chr22: 19,040,083-19,134,296	GSC2, LOC112268289, 9 more genes
nsv7029753	copy number variation	1	nstd229	human		GRCh38 chr22: 19,119,501-19,207,400 , GRCh37.p13 chr22: 19,134,297-19,194,910 , GRCh37.p13 chr22\|NW_003871096.1: 1-60,617	CLTCL1, DGCR2, 8 more genes
nsv7025539	copy number variation	1	nstd229	human		GRCh38 chr22: 19,038,989-19,265,869 , GRCh37.p13 chr22: 19,134,297-19,253,392 , GRCh37.p13 chr22\|NW_003871096.1: 1-119,086	LOC100129262, LINC01311, 13 more genes
nsv7024839	copy number variation	1	nstd229	human		GRCh38 chr22: 19,092,545-19,196,242 , GRCh37.p13 chr22: 19,080,058-19,134,296	SLC25A1, ESS2, 8 more genes
nsv6638022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,916,843-21,075,592 , GRCh38.p12 chr22: 18,339,130-20,721,304	FAM230J, LOC107985588, 107 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 678

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 678

Page of 34

Number of Variants: 20

Page of 34

Supplemental Content

Find related data

Recent activity