dcps[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
nsv4675974	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 126,201,307-126,466,438 , GRCh38.p12 chr11: 126,331,412-126,596,543	DCPS, ST3GAL4, 2 more genes
nsv3911009	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 119,424,297-135,075,271 , NCBI36 chr11: 118,800,217-134,450,377 , GRCh37 chr11: 119,295,007-134,945,165	DCPS, PHB1P17, 304 more genes
nsv3922773	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 119,304,619-134,868,407 , GRCh38 chr11: 119,433,909-134,998,513 , NCBI36 chr11: 118,809,829-134,373,617	DCPS, ETS1-AS1, 301 more genes
nsv3906843	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 119,538,664-134,938,470 , GRCh38.p12 chr11: 119,667,954-135,068,576	DCPS, TMEM225, 296 more genes
nsv3902675	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 119,807,473-134,868,407 , GRCh38.p12 chr11: 119,936,764-134,998,513	DCPS, FEZ1, 291 more genes
nsv3923251	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 119,891,678-134,450,377 , GRCh38 chr11: 120,515,759-135,075,271 , GRCh37 chr11: 120,386,468-134,945,165	DCPS, KIRREL3-AS3, 279 more genes
nsv3901752	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,527,021-134,938,470 , GRCh38.p12 chr11: 120,656,312-135,068,576	DCPS, LOC105369534, 276 more genes
nsv4436748	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,576,984-134,934,063 , GRCh38.p12 chr11: 120,706,275-135,064,169	DCPS, LINC02098, 276 more genes
nsv3904760	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,615,374-134,868,407 , GRCh38.p12 chr11: 120,744,665-134,998,513	DCPS, OR8D2, 275 more genes
nsv4675832	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,742,540-134,938,470 , GRCh38.p12 chr11: 120,871,831-135,068,576	DCPS, MIR8052, 275 more genes
nsv3924566	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 120,507,265-134,576,266 , NCBI36 chr11: 119,883,184-133,951,370 , GRCh37 chr11: 120,377,974-134,446,160	DCPS, CCDC15-DT, 271 more genes
nsv3891701	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 121,136,603-134,938,470 , GRCh38.p12 chr11: 121,265,894-135,068,576	DCPS, OR10G9, 266 more genes
nsv7137129	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659	DCPS, VSIG10L2, 268 more genes
nsv3895234	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 121,416,261-134,938,470 , GRCh38.p12 chr11: 121,545,552-135,068,576	DCPS, SF3A3P2, 262 more genes
nsv3918400	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 121,482,185-134,938,470 , GRCh38 chr11: 121,611,476-135,068,576 , NCBI36 chr11: 120,987,395-134,443,680	DCPS, RN7SL167P, 262 more genes
nsv3915295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 121,064,970-134,450,377 , GRCh38 chr11: 121,689,052-135,075,271 , GRCh37 chr11: 121,559,760-134,945,165	DCPS, LOC105369591, 262 more genes
nsv3892434	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 121,501,072-134,868,348 , GRCh38.p12 chr11: 121,630,363-134,998,454	DCPS, ZNF123P, 261 more genes
nsv3919969	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 121,780,459-135,075,271 , GRCh37 chr11: 121,651,167-134,945,165 , NCBI36 chr11: 121,156,377-134,450,377	DCPS, STT3A-AS1, 262 more genes
nsv3915055	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 121,184,838-134,452,384 , GRCh37.p13 chr11: 121,679,628-134,946,516 , GRCh38.p12 chr11: 121,808,920-135,076,622	DCPS, KIRREL3, 262 more genes
nsv3912600	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 121,806,547-135,068,576 , GRCh37 chr11: 121,677,255-134,938,470 , NCBI36 chr11: 121,182,465-134,443,680	DCPS, RN7SKP121, 261 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 69

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 69

Page of 4

Number of Variants: 20

Page of 4

Supplemental Content

Find related data

Search details

Recent activity