ap1ar[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
nsv3877909	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 110,853,395-114,363,395 , NCBI36 chr4: 111,994,000-115,504,000 , GRCh37 chr4: 111,774,551-115,284,551	AP1AR, LOC105377374, 51 more genes
nsv4729714	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 111,334,313-113,223,858 , GRCh38.p12 chr4: 110,413,157-112,302,702	AP1AR, PANCR, 20 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	AP1AR, 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	AP1AR, 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	AP1AR, 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	AP1AR, 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	AP1AR, 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	AP1AR, 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	AP1AR, 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	AP1AR, 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	AP1AR, 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	AP1AR, MIR576, 447 more genes
nsv3911834	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr4: 112,210,390-117,832,483 , GRCh37 chr4: 111,990,941-117,613,035 , GRCh38 chr4: 111,069,785-116,691,879	AP1AR, ANK2, 71 more genes
nsv6313895	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 112,849,108-115,434,557 , GRCh38.p12 chr4: 111,927,952-114,513,401	AP1AR, ANK2, 45 more genes
nsv7098984	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr4: 110,650,730-112,833,790 , GRCh37.p13 chr4: 111,571,886-113,754,946	AP1AR, ANK2, 36 more genes
nsv3870900	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 113,175,966-113,835,185 , GRCh38.p12 chr4: 112,254,810-112,914,029	AP1AR, ANK2, 23 more genes
nsv3872829	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 112,901,280-113,403,129 , GRCh38.p12 chr4: 111,980,124-112,481,973	AP1AR, RTEL1P1, 9 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	AP1AR, RNU7-194P, 939 more genes
nsv6315356	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 112,481,911-113,756,889 , GRCh38.p12 chr4: 111,560,755-112,835,733	AP1AR, RPL36AP19, 31 more genes
nsv4455835	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 113,116,277-113,602,286 , GRCh38.p12 chr4: 112,195,121-112,681,130	AP1AR, MIR367, 16 more genes

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Items: 20

Number of Variants: 20

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