clock[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3871446	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 56,225,485-56,300,646 , GRCh38.p12 chr4: 55,359,318-55,434,479	CLOCK, TMEM165, 3 more genes
nsv4456591	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 56,366,390-56,436,379 , GRCh38.p12 chr4: 55,500,223-55,570,212	CLOCK, PDCL2, 1 more genes
nsv5674237	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872	CLOCK, FTLP10, 335 more genes
nsv3917232	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 54,759,525-62,818,428 , GRCh38 chr4: 54,198,601-62,270,115 , GRCh37 chr4: 55,064,768-63,135,833	CLOCK, TMEM165, 84 more genes
nsv3912235	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 52,639,018-59,984,479 , GRCh37 chr4: 53,505,185-60,850,197 , NCBI36 chr4: 53,199,942-60,532,792	CLOCK, LOC105377672, 97 more genes
nsv6291206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,685,685-58,104,722 , GRCh38.p12 chr4: 51,819,519-57,238,556	CLOCK, SRD5A3, 96 more genes
nsv6315421	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 53,688,710-56,491,447 , GRCh38.p12 chr4: 52,822,543-55,625,280	CLOCK, METTL5P3, 38 more genes
nsv7097256	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr4: 55,124,936-57,368,027 , GRCh38.p12 chr4: 54,258,769-56,501,861	CLOCK, AASDH, 40 more genes
nsv3873978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724	CLOCK, LOC100422029, 2358 more genes
nsv3876533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611	CLOCK, LOC100420289, 2347 more genes
nsv3884499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286	CLOCK, MTND4LP29, 2341 more genes
nsv3880085	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318	CLOCK, LOC112268460, 2345 more genes
nsv3883791	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495	CLOCK, LOC105377343, 2341 more genes
nsv6291432	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354	CLOCK, SNHG27, 1091 more genes
nsv3872797	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-66,440,622 , GRCh38.p12 chr4: 68,453-65,574,904	CLOCK, GNPDA2, 813 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	CLOCK, OR7E84P, 764 more genes
nsv3913811	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 51,831,622-97,505,618 , GRCh37 chr4: 52,697,788-98,426,769 , NCBI36 chr4: 52,392,545-98,645,792	CLOCK, LOC105377297, 582 more genes
nsv3914335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 44,358,218-63,111,600 , NCBI36 chr4: 44,052,975-62,794,195 , GRCh38 chr4: 44,356,201-62,245,882	CLOCK, RPL22P13, 178 more genes
nsv3910089	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 52,392,545-67,539,802 , GRCh37 chr4: 52,697,788-67,857,207 , GRCh38 chr4: 51,831,622-66,991,489	CLOCK, LINC02260, 154 more genes
nsv3919213	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,766,026-60,850,197 , NCBI36 chr4: 52,460,783-60,532,792 , GRCh38 chr4: 51,899,860-59,984,479	CLOCK, LNX1-AS1, 106 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:

Search results

Items: 1 to 20 of 22

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

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

Search results

Items: 1 to 20 of 22

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity