dbVar for Gene (Select 101927913) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4456780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393	LOC105374960, LOC101928573, 342 more genes
nsv3923249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 110,675-8,981,266 , GRCh38 chr6: 165,675-9,036,034 , GRCh37 chr6: 165,675-9,036,267	LOC100506207, LOC105374889, 148 more genes
nsv3922576	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 164,633-6,284,470 , GRCh38 chr6: 164,633-6,284,237 , NCBI36 chr6: 109,633-6,229,469	GLRX3P2, CDYL, 106 more genes
nsv3922052	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 155,807-17,058,645 , NCBI36 chr6: 100,807-17,166,624 , GRCh38 chr6: 155,807-17,058,414	ECI2-DT, RNU1-11P, 268 more genes
nsv3921817	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 2,862,874-16,698,019 , GRCh38 chr6: 2,862,640-16,697,788 , NCBI36 chr6: 2,807,873-16,805,998	RN7SKP293, LOC105374906, 230 more genes
nsv3921201	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 101,974-4,892,090 , GRCh37 chr6: 156,974-4,947,091 , GRCh38 chr6: 156,974-4,946,857	LOC100422781, RN7SL352P, 86 more genes
nsv3921027	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 389,423-13,474,956 , GRCh37 chr6: 389,423-13,475,188 , NCBI36 chr6: 334,423-13,583,167	LOC105374898, HIVEP1, 215 more genes
nsv3920564	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946	PRELID1P2, RPL7AP7, 785 more genes
nsv3920236	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 164,633-5,823,834 , GRCh38 chr6: 164,633-5,823,601 , NCBI36 chr6: 109,633-5,768,833	TUBB2A, SERPINB9-AS1, 98 more genes
nsv3919014	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 4,427,090-8,391,140 , NCBI36 chr6: 4,372,323-8,336,372 , GRCh37 chr6: 4,427,324-8,391,373	RREB1, FARS2, 65 more genes
nsv3918645	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr6: 101,974-11,659,036 , GRCh37 chr6: 156,974-11,551,050 , GRCh38 chr6: 156,974-11,550,817	BMP6, BPHL, 194 more genes
nsv3917576	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 144,957-5,239,181 , NCBI36 chr6: 89,957-5,184,413 , GRCh37 chr6: 144,957-5,239,414	MIR3691, PRPF4B, 94 more genes
nsv3916436	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 156,974-7,122,992 , NCBI36 chr6: 101,974-7,067,991 , GRCh38 chr6: 156,974-7,122,759	LINC01011, FOXF2, 119 more genes
nsv3916403	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-4,907,692 , GRCh37 chr6: 156,974-4,907,926 , NCBI36 chr6: 101,974-4,852,925	MIR6720, LOC643327, 86 more genes
nsv3915132	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 152,634-5,315,912 , GRCh38 chr6: 152,634-5,315,679 , NCBI36 chr6: 97,634-5,260,911	LOC101927888, PSMC1P11, 94 more genes
nsv3914814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 163,083-6,063,033 , GRCh38 chr6: 163,083-6,062,800 , NCBI36 chr6: 108,083-6,008,032	LINC02521, PKMP5, 103 more genes
nsv3914672	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr6: 101,974-13,189,419 , GRCh37 chr6: 156,974-13,081,433 , GRCh38 chr6: 156,974-13,081,201	BMP6, BPHL, 212 more genes
nsv3914400	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 97,634-6,235,036 , GRCh38 chr6: 152,634-6,289,804 , GRCh37 chr6: 152,634-6,290,037	LOC105374898, SERPINB9-AS1, 106 more genes
nsv3914068	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 4,014,025-13,376,010 , GRCh38 chr6: 4,068,792-13,267,799 , GRCh37 chr6: 4,069,026-13,268,031	SSR1, LOC107986560, 145 more genes
nsv3913920	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028	TRR-ACG1-2, TMEM217, 1385 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 134

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 134

Page of 7

Number of Variants: 20

Page of 7

Supplemental Content

Find related data

Recent activity