fbxw7[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
nsv3888965	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 153,242,605-153,315,320 , GRCh38.p12 chr4: 152,321,453-152,394,168	FBXW7, FBXW7-AS1
nsv4578400	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 153,244,033-153,332,955 , GRCh38.p12 chr4: 152,322,881-152,411,803	FBXW7, FBXW7-AS1
nsv3883790	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 153,248,578-153,425,502 , GRCh38.p12 chr4: 152,327,426-152,504,350	FBXW7, MIR3140, 1 more genes
nsv3871140	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 153,195,089-153,451,356 , GRCh38.p12 chr4: 152,273,937-152,530,204	FBXW7, LOC105377492, 2 more genes
nsv3871338	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 153,242,605-153,452,160 , GRCh38.p12 chr4: 152,321,453-152,531,008	FBXW7, FBXW7-AS1, 1 more genes
nsv3878475	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 153,242,605-153,451,356 , GRCh38.p12 chr4: 152,321,453-152,530,204	FBXW7, FBXW7-AS1, 1 more genes
nsv3885864	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 153,184,316-153,334,717 , GRCh38.p12 chr4: 152,263,164-152,413,565	FBXW7, RN7SL446P, 2 more genes
nsv3871565	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 153,390,057-153,519,781 , GRCh38.p12 chr4: 152,468,905-152,598,629	FBXW7, MIR4453HG, 3 more genes
nsv3874224	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 153,203,431-162,912,359 , GRCh38.p12 chr4: 152,282,279-161,991,207	FBXW7, PLRG1, 120 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	FBXW7, 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	FBXW7, 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	FBXW7, 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	FBXW7, 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	FBXW7, LOC105377343, 2341 more genes
nsv3875534	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 93,071,152-190,957,473 , GRCh38.p12 chr4: 92,150,001-190,036,318	FBXW7, KLKB1, 1118 more genes
nsv3874596	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 109,199,664-189,752,726 , GRCh38.p12 chr4: 108,278,508-188,831,572	FBXW7, RPL6P12, 938 more genes
nsv3924008	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 118,065,569-190,042,639 , GRCh37 chr4: 118,986,724-190,828,225 , NCBI36 chr4: 119,206,172-191,200,788	FBXW7, PPID, 828 more genes
nsv3874610	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 119,437,495-190,904,301 , GRCh38.p12 chr4: 118,516,340-189,983,146	FBXW7, OTUD4, 813 more genes
nsv3918110	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 122,658,828-191,220,419 , GRCh38 chr4: 121,518,223-190,062,270 , GRCh37 chr4: 122,439,378-190,828,225	FBXW7, SCRG1, 770 more genes
nsv4455301	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 124,873,497-185,278,662 , GRCh38.p12 chr4: 123,952,342-184,357,509	FBXW7, SMARCA5, 633 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 38

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Number of Variants: 20

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Supplemental Content

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