dbVar for Gene (Select 79155) - dbVar

loading data ...

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
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
nsv7053632	inversion	1	nstd229	human		GRCh38 chr4: 2,573,854-2,771,716 , GRCh37.p13 chr4: 2,575,581-2,773,443	TNIP2, FAM193A, 1 more genes
nsv7049289	inversion	1	nstd229	human		GRCh38 chr4: 1,879,237-2,966,412 , GRCh37.p13 chr4: 1,880,964-2,968,139	RNF4, SCARNA22, 28 more genes
nsv7040457	inversion	1	nstd229	human		GRCh38 chr4: 2,747,436-3,221,045 , GRCh37.p13 chr4: 2,749,163-3,222,772	HTT, NOP14-AS1, 10 more genes
nsv7039441	inversion	1	nstd229	human		GRCh38 chr4: 1,689,472-2,959,448 , GRCh37.p13 chr4: 1,691,199-2,961,175	NOP14-AS1, LOC112268460, 34 more genes
nsv6728046	copy number variation	1	nstd229	human		GRCh38 chr4: 2,734,575-2,749,686 , GRCh37.p13 chr4: 2,736,302-2,751,413	TNIP2
nsv6726977	copy number variation	1	nstd229	human		GRCh38 chr4: 2,748,610-2,748,746 , GRCh37.p13 chr4: 2,750,337-2,750,473	TNIP2
nsv6722104	copy number variation	1	nstd229	human		GRCh38 chr4: 2,747,477-2,785,731 , GRCh37.p13 chr4: 2,749,204-2,787,458	TNIP2, LOC102723763
nsv6718318	copy number variation	1	nstd229	human		GRCh38 chr4: 2,601,931-2,745,234 , GRCh37.p13 chr4: 2,603,658-2,746,961	FAM193A, TNIP2
nsv6637043	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 2,619,318-2,849,268 , GRCh38.p12 chr4: 2,617,591-2,847,541	FAM193A, TNIP2, 3 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
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
nsv6557395	inversion	1	nstd223	human		GRCh38 chr4: 2,505,523-2,780,999 , GRCh37.p13 chr4: 2,507,250-2,782,726	RNF4, FAM193A, 2 more genes
nsv6363673	copy number variation	1	nstd223	human		GRCh38 chr4: 2,748,610-2,748,746 , GRCh37.p13 chr4: 2,750,337-2,750,473	TNIP2
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
nsv6315365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-5,579,467 , GRCh38.p12 chr4: 68,453-5,577,740	LOC107986246, FAM53A, 149 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 329

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 329

Page of 17

Number of Variants: 20

Page of 17

Supplemental Content

Find related data

Recent activity