arsj[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
nsv4674758	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 114,868,539-115,175,427 , GRCh38.p12 chr4: 113,947,383-114,254,271	ARSJ, LOC105377376, 1 more genes
nsv4674426	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 114,868,539-114,954,676 , GRCh38.p12 chr4: 113,947,383-114,033,520	ARSJ, LOC107986305, 1 more genes
nsv6636899	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 114,661,111-115,170,981 , GRCh38.p12 chr4: 113,739,955-114,249,825	ARSJ, LOC105377376, 3 more genes
nsv6290265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 114,872,547-138,005,267 , GRCh38.p12 chr4: 113,951,391-137,084,113	ARSJ, LOC105379404, 218 more genes
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	ARSJ, LOC105377374, 51 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	ARSJ, 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	ARSJ, 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	ARSJ, 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	ARSJ, 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	ARSJ, 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	ARSJ, 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	ARSJ, 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	ARSJ, 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	ARSJ, 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	ARSJ, 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	ARSJ, 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	ARSJ, ANK2, 45 more genes
nsv6636328	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 114,535,234-115,262,363 , GRCh38.p12 chr4: 113,614,078-114,341,207	ARSJ, LOC105377376, 5 more genes
nsv3915435	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 114,831,780-115,517,385 , GRCh37.p13 chr4: 114,612,331-115,297,936 , GRCh38.p12 chr4: 113,691,175-114,376,780	ARSJ, LOC107986305, 5 more genes
nsv6636983	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 114,635,932-115,251,586 , GRCh38.p12 chr4: 113,714,776-114,330,430	ARSJ, LOC107986305, 4 more genes

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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 23

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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