foxred1[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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	FOXRED1, 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	FOXRED1, 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	FOXRED1, 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	FOXRED1, 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	FOXRED1, 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	FOXRED1, 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	FOXRED1, 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	FOXRED1, 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	FOXRED1, 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	FOXRED1, 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	FOXRED1, 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	FOXRED1, 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	FOXRED1, 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	FOXRED1, 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	FOXRED1, 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	FOXRED1, 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	FOXRED1, 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	FOXRED1, 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	FOXRED1, RN7SKP121, 261 more genes
nsv6637558	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 122,975,824-134,938,470 , GRCh38.p12 chr11: 123,105,116-135,068,576	FOXRED1, OR8B8, 234 more genes

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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 70

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Number of Variants: 20

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