egf[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4682288	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 65,639,431-65,640,415 , GRCh38.p12 chr11: 65,871,960-65,872,944	EFEMP2
nsv3879412	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 110,840,748-110,862,637 , GRCh38.p12 chr4: 109,919,592-109,941,481	EGF
nsv3885071	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 110,834,150-110,845,707 , GRCh38.p12 chr4: 109,912,994-109,924,551	EGF
nsv6311996	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 110,862,082-110,901,315 , GRCh38.p12 chr4: 109,940,926-109,980,159	EGF
nsv7096828	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 110,834,110-110,932,611 , GRCh38.p12 chr4: 109,912,954-110,011,455	EGF, RNU6-35P
nsv6309442	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 65,634,389-65,639,825 , GRCh38.p12 chr11: 65,866,918-65,872,354	EFEMP2, MUS81
nsv3873978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724	EGF, 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	EGF, 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	EGF, 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	EGF, 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	EGF, 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	EGF, KLKB1, 1118 more genes
nsv6291432	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354	EGF, SNHG27, 1091 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	EGF, RPL6P12, 938 more genes
nsv6313878	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443	EGF, LINC00613, 448 more genes
nsv3920388	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 97,014,044-137,331,362 , NCBI36 chr4: 97,233,067-137,550,812 , GRCh38 chr4: 96,092,893-136,410,207	EGF, MIR576, 447 more genes
nsv3920136	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 106,699,504-111,128,029 , GRCh38 chr4: 105,778,347-110,206,873 , NCBI36 chr4: 106,918,953-111,347,478	EGF, AIMP1, 58 more genes
nsv3913029	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 110,721,397-110,911,297 , GRCh38 chr4: 109,800,241-109,990,141 , NCBI36 chr4: 110,940,846-111,130,746	EGF, KRT19P3, 4 more genes
nsv4453555	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr11: 65,866,431-66,347,555 , GRCh37 chr11: 65,633,902-66,115,026	CNIH2, YIF1A, 33 more genes

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egf[All Fields] AND 1[has_clinical] (20)
dbVar
Clec4a1 C-type lectin domain family 4, member a1 [Mus musculus]
Clec4a1 C-type lectin domain family 4, member a1 [Mus musculus]
Gene ID:269799

Gene
Gene Links for GEO Profiles (Select 18799873) (1)
Gene
D930019O06Rik RIKEN cDNA D930019O06 [Mus musculus]
D930019O06Rik RIKEN cDNA D930019O06 [Mus musculus]
Gene ID:425051

Gene
Gene Links for GEO Profiles (Select 18799279) (1)
Gene

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