elovl6[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
nsv3887481	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 111,004,011-111,004,898 , GRCh38.p12 chr4: 110,082,855-110,083,742	ELOVL6
nsv3885603	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 111,079,337-111,173,378 , GRCh38.p12 chr4: 110,158,181-110,252,222	ELOVL6, HSBP1P2
nsv3880806	copy number variation	1	nstd102	human	not provided	GRCh38 chr4: 110,158,181-110,266,527 , GRCh37 chr4: 111,079,337-111,187,683	ELOVL6, HSBP1P2
nsv3910912	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 111,164,908-111,454,520 , GRCh37 chr4: 110,945,459-111,235,071 , GRCh38 chr4: 110,024,303-110,313,915	ELOVL6, RNU6-205P, 3 more genes
esv3648194	copy number variation	1	estd216	human	not provided	GRCh38.p12 chr4: 110,158,181-110,266,527 , GRCh37 chr4: 111,079,337-111,187,683	ELOVL6, HSBP1P2, 1 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	ELOVL6, 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	ELOVL6, 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	ELOVL6, 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	ELOVL6, 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	ELOVL6, 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	ELOVL6, 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	ELOVL6, 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	ELOVL6, 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	ELOVL6, 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	ELOVL6, 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	ELOVL6, AIMP1, 58 more genes
nsv3916316	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 111,318,515-191,263,063 , GRCh37.p13 chr4: 111,099,066-191,029,082 , GRCh38.p12 chr4: 110,177,910-190,107,927	ELOVL6, RNU7-194P, 939 more genes

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