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

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Items: 17

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3877023	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 101,595,019-101,601,421 , GRCh38.p12 chr4: 100,673,862-100,680,264	LINC01216
nsv3889341	copy number variation	1	nstd102	human	not provided	GRCh37 chr4: 101,568,956-101,616,281 , GRCh38 chr4: 100,647,799-100,695,124	LINC01216
esv3648190	copy number variation	1	estd216	human	not provided	GRCh37 chr4: 101,568,956-101,616,281 , GRCh38.p12 chr4: 100,647,799-100,695,124	LINC01216
nsv3923759	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 58,862,002-102,129,682 , GRCh37.p13 chr4: 59,167,245-101,910,659 , GRCh38.p12 chr4: 58,301,079-100,989,502	EMCN, EREG, 530 more genes
nsv3923733	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 80,427,023-100,855,441 , GRCh37 chr4: 81,348,177-101,776,598 , NCBI36 chr4: 81,567,201-101,995,621	EMCN, PDLIM5, 215 more genes
nsv3885328	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 92,201,567-103,043,808 , GRCh38.p12 chr4: 91,280,416-102,122,651	EMCN, TRMT10A, 86 more genes
nsv3910689	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 92,610,413-101,521,991 , GRCh37 chr4: 93,531,564-102,443,148 , NCBI36 chr4: 93,750,587-102,662,171	EMCN, GRID2, 77 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	EMCN, 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	EMCN, 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	EMCN, 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	EMCN, 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	EMCN, 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	EMCN, 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	EMCN, SNHG27, 1091 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	EMCN, MIR576, 447 more genes
nsv6291428	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 95,490,755-109,977,216 , GRCh38.p12 chr4: 94,569,604-109,056,060	EMCN, ADH1A, 157 more genes
nsv3920440	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 101,719,190-102,662,230 , GRCh37 chr4: 101,500,167-102,443,207 , GRCh38 chr4: 100,579,010-101,522,050	FLJ20021, LINC01216, 4 more genes

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emcn[All Fields] AND 1[has_clinical] (19)
dbVar
Gene Links for Protein (Select 2217372567) (1)
Gene
PAG1 phosphoprotein membrane anchor with glycosphingolipid microdomains 1 [Homo ...
PAG1 phosphoprotein membrane anchor with glycosphingolipid microdomains 1 [Homo sapiens]
Gene ID:55824

Gene

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