cldn1[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
nsv4347470	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 190,039,387-190,040,504 , GRCh38.p12 chr3: 190,321,598-190,322,715	CLDN1, CLDN16
nsv6313726	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 189,910,071-190,132,466 , GRCh38.p12 chr3: 190,192,282-190,414,677	CLDN1, CLDN16
nsv3914069	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 191,434,475-191,699,411 , GRCh38 chr3: 190,233,992-190,498,928 , GRCh37 chr3: 189,951,781-190,216,717	CLDN1, TMEM207, 1 more genes
nsv3915488	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 185,203,637-197,837,049 , NCBI36 chr3: 186,686,331-199,321,446 , GRCh38 chr3: 185,485,849-198,110,178	CLDN1, SNAR-I, 260 more genes
nsv3914166	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 180,856,452-192,229,812 , GRCh38 chr3: 181,138,664-192,512,023 , NCBI36 chr3: 182,339,146-193,712,506	CLDN1, SNORA4, 199 more genes
nsv3920607	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 187,082,628-197,946,692 , GRCh37.p13 chr3: 185,599,934-196,462,295 , GRCh38.p12 chr3: 185,882,146-196,735,424	CLDN1, FGF12, 212 more genes
nsv3872972	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 189,101,446-197,838,262 , GRCh38.p12 chr3: 189,383,657-198,111,391	CLDN1, TMEM44, 187 more genes
nsv3882335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,650,681-191,275,809 , GRCh38.p12 chr3: 182,932,893-191,558,020	CLDN1, VPS8, 171 more genes
nsv6290259	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 189,608,636-197,532,175 , GRCh38.p12 chr3: 189,890,847-197,805,304	CLDN1, LINC01972, 174 more genes
nsv3918718	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 186,482,937-194,130,145 , NCBI36 chr3: 187,965,631-195,611,434 , GRCh38 chr3: 186,765,148-194,409,416	CLDN1, TPRG1-AS1, 114 more genes
nsv3920718	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 188,646,713-196,231,151 , GRCh37 chr3: 187,164,019-194,749,862 , GRCh38 chr3: 187,446,231-195,029,133	CLDN1, LOC105374283, 105 more genes
nsv3884529	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 186,291,045-191,037,240 , GRCh38.p12 chr3: 186,573,256-191,319,451	CLDN1, TPRG1-AS2, 75 more genes
nsv3923340	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 187,446,231-190,839,052 , GRCh37 chr3: 187,164,019-190,556,841 , NCBI36 chr3: 188,646,713-192,039,535	CLDN1, ENOPH1P1, 36 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	CLDN1, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	CLDN1, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	CLDN1, RPL23AP49, 2875 more genes
nsv3918981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446	CLDN1, LINC02614, 1469 more genes
nsv3918692	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833	CLDN1, LOC105374179, 785 more genes
nsv3874894	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 142,995,020-192,997,215 , GRCh38.p12 chr3: 143,276,178-193,279,426	CLDN1, RNU6-901P, 673 more genes
nsv3918066	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 152,100,512-198,118,383 , NCBI36 chr3: 153,300,991-199,329,651 , GRCh37 chr3: 151,818,301-197,845,254	CLDN1, LOC105374260, 696 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 45

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Number of Variants: 20

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