fbxw4[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
nsv3891205	copy number variation	1	nstd102	human	not provided	GRCh37 chr10: 103,421,890-103,458,708 , GRCh38.p12 chr10: 101,662,133-101,698,951	FBXW4
nsv3913916	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 103,358,841-103,436,241 , GRCh38 chr10: 101,599,084-101,676,484 , NCBI36 chr10: 103,348,831-103,426,231	FBXW4, MIR3158-2, 3 more genes
nsv4455818	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 103,362,038-103,392,888 , GRCh38.p12 chr10: 101,602,281-101,633,131	FBXW4, RNU6-1165P, 1 more genes
nsv3919300	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 103,166,019-103,439,322 , GRCh37 chr10: 103,176,029-103,449,332 , GRCh38 chr10: 101,416,272-101,689,575	FBXW4, BTRC, 5 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	FBXW4, RNU7-12P, 1876 more genes
nsv3920295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422	FBXW4, EIF2S2P3, 895 more genes
nsv3914943	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 101,297,763-101,618,190 , NCBI36 chr10: 103,047,510-103,367,937 , GRCh37 chr10: 103,057,520-103,377,947	FBXW4, BTRC, 6 more genes
nsv3891720	copy number variation	1	nstd102	human	Pathogenic	GRCh38.p12 chr10: 101,449,047-101,689,516 , GRCh37 chr10: 103,208,804-103,449,273	FBXW4, BTRC, 5 more genes
nsv3906389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996	FBXW4, LOC100419870, 2105 more genes
nsv3891157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558	FBXW4, AGAP14P, 2097 more genes
nsv3902271	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639	FBXW4, ANXA11, 2085 more genes
nsv3891958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414	FBXW4, TUBB8, 2085 more genes
nsv7137211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639	FBXW4, EXOC6, 1906 more genes
nsv3905489	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,283,493-135,427,143 , GRCh38.p12 chr10: 91,523,736-133,613,639	FBXW4, LOC105378476, 688 more genes
nsv3890046	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 94,346,520-135,427,143 , GRCh38.p12 chr10: 92,586,763-133,613,639	FBXW4, UROS, 667 more genes
nsv3921919	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 100,600,492-133,622,588 , GRCh37 chr10: 102,360,249-135,436,092 , NCBI36 chr10: 102,350,239-135,286,082	FBXW4, MIR4295, 508 more genes
nsv3898332	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 103,288,313-135,512,075 , GRCh38.p12 chr10: 101,528,556-133,774,750	FBXW4, NPS, 503 more genes
nsv3923769	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291	FBXW4, LOC105378493, 477 more genes
nsv3909942	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 96,872,364-118,383,651 , GRCh38 chr10: 95,112,607-116,776,637 , NCBI36 chr10: 96,862,354-118,526,138	FBXW4, LOC102723665, 360 more genes
nsv4349819	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 102,822,575-103,558,868 , GRCh38.p12 chr10: 101,062,818-101,799,111	FBXW4, LBX1, 22 more genes

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Number of Variants: 20

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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 49

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Number of Variants: 20

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Supplemental Content

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Search details

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