tspan5[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
nsv3873468	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 99,527,572-99,687,168 , GRCh38.p12 chr4: 98,606,421-98,766,017	TSPAN5, BTF3P13, 3 more genes
nsv3910713	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 99,305,549-99,652,783 , GRCh37.p13 chr4: 99,086,526-99,433,760 , GRCh38.p12 chr4: 98,165,375-98,512,609	TSPAN5, RAP1GDS1, 2 more genes
nsv4456683	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 99,513,451-99,603,864 , GRCh38.p12 chr4: 98,592,300-98,682,713	TSPAN5, TSPAN5-DT, 1 more genes
nsv4455945	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 99,521,332-99,600,079 , GRCh38.p12 chr4: 98,600,181-98,678,928	TSPAN5, LOC112267901, 1 more genes
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	TSPAN5, 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	TSPAN5, PDLIM5, 215 more genes
nsv7148241	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930	TSPAN5, LOC105377327, 214 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	TSPAN5, 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	TSPAN5, 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	TSPAN5, 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	TSPAN5, 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	TSPAN5, 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	TSPAN5, 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	TSPAN5, 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	TSPAN5, 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	TSPAN5, 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	TSPAN5, MIR576, 447 more genes
nsv4729197	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 94,692,345-101,308,220 , GRCh38.p12 chr4: 93,771,194-100,387,063	TSPAN5, ADH1A, 66 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	TSPAN5, ADH1A, 157 more genes
nsv3886649	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr4: 99,288,284-99,846,320 , GRCh38.p12 chr4: 98,367,133-98,925,169	TSPAN5, TBCAP3, 8 more genes

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Number of Variants: 20

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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 24

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Number of Variants: 20

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Supplemental Content

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Search details

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