fbxo39[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
nsv6291524	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 6,630,436-6,811,274 , GRCh38.p12 chr17: 6,727,117-6,907,955	FBXO39, ALOX12P2, 3 more genes
nsv4675132	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 6,630,435-6,800,894 , GRCh38.p12 chr17: 6,727,116-6,897,575	FBXO39, TEKT1, 3 more genes
nsv6314075	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 6,630,435-6,778,040 , GRCh38.p12 chr17: 6,727,116-6,874,721	FBXO39, ALOX12P2, 3 more genes
nsv3913013	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055	FBXO39, RPS4XP17, 289 more genes
nsv3915884	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 45,835-6,862,369 , GRCh38 chr17: 162,088-6,959,050 , NCBI36 chr17: 11,879-6,803,093	FBXO39, LOC105371592, 222 more genes
nsv3923152	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 3,451,558-7,022,067 , GRCh38 chr17: 3,601,515-7,178,024 , GRCh37 chr17: 3,504,809-7,081,343	FBXO39, PSMB6, 133 more genes
nsv3910343	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 5,636,297-7,942,140 , NCBI36 chr17: 5,577,021-7,882,865 , GRCh38 chr17: 5,732,977-8,038,822	FBXO39, RPL23AP73, 106 more genes
nsv5673052	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 6,589,506-7,128,436 , GRCh38.p12 chr17: 6,686,187-7,225,117	FBXO39, RPL23AP73, 25 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	FBXO39, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	FBXO39, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	FBXO39, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	FBXO39, SMURF2, 2366 more genes
nsv3897625	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-15,027,737 , GRCh38.p12 chr17: 150,732-15,124,420	FBXO39, GP1BA, 439 more genes
nsv3915354	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519	FBXO39, KIF1C-AS1, 433 more genes
nsv3917059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901	FBXO39, PSMB6, 409 more genes
nsv7148254	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413	FBXO39, RFLNB, 401 more genes
nsv3904771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-11,186,432 , GRCh38.p12 chr17: 150,732-11,283,115	FBXO39, SLC2A4, 401 more genes
nsv3917777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 50,690-7,394,448 , GRCh38 chr17: 198,748-7,491,129 , NCBI36 chr17: 48,539-7,335,172	FBXO39, PAFAH1B1, 267 more genes
nsv3911050	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 5,732,953-12,095,349 , GRCh37 chr17: 5,636,273-11,998,666 , NCBI36 chr17: 5,576,997-11,939,391	FBXO39, C17orf49, 209 more genes
nsv3904710	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 1,113,102-6,742,486 , GRCh38.p12 chr17: 1,209,808-6,839,167	FBXO39, OR1A2, 197 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 26

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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