cldn23[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
nsv4729244	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 8,547,930-8,681,444 , GRCh38.p12 chr8: 8,690,420-8,823,934 , GRCh38.p12 chr8\|NW_018654717.1: 4,528,062-4,661,689	CLDN23, MFHAS1
nsv3890708	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr8: 8,396,736-8,629,734 , GRCh38.p12 chr8: 8,539,226-8,772,224 , GRCh38.p12 chr8\|NW_018654717.1: 4,579,941-4,812,872	CLDN23, LOC105379225, 2 more genes
nsv3897142	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 8,407,886-8,629,936 , GRCh38.p12 chr8: 8,550,376-8,772,426 , GRCh38.p12 chr8\|NW_018654717.1: 4,579,739-4,801,747	CLDN23, LOC105379225, 2 more genes
nsv6636765	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 8,409,391-8,729,438 , GRCh38.p12 chr8: 8,551,881-8,871,928 , GRCh38.p12 chr8\|NW_018654717.1: 4,480,057-4,800,242	CLDN23, MFHAS1, 3 more genes
nsv6315449	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940	CLDN23, LOC101928016, 568 more genes
nsv3917350	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 2,292,235-27,361,796 , GRCh38 chr8: 2,475,295-27,504,279 , NCBI36 chr8: 2,121,457-27,417,713	CLDN23, LINC03022, 472 more genes
nsv7148253	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417	CLDN23, ENTPD4, 447 more genes
nsv6636968	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-18,936,715 , GRCh38.p12 chr8: 208,049-19,079,205	CLDN23, ZNF705B, 357 more genes
nsv4455719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-14,214,722 , GRCh38.p12 chr8: 208,048-14,357,213	CLDN23, MIR598, 312 more genes
nsv4685988	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 161,516-11,516,619 , GRCh38.p12 chr8: 211,516-11,659,110	CLDN23, ZNF705B, 232 more genes
nsv7148131	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 10,501-11,142,629 , GRCh38.p12 chr8: 60,501-11,285,120	CLDN23, XKR6, 224 more genes
nsv6634376	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-11,281,408 , GRCh38.p12 chr8: 208,048-11,423,899	CLDN23, DLGAP2-AS1, 228 more genes
nsv6636940	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-10,965,627 , GRCh38.p12 chr8\|NW_018654717.1: 1-5,513,617 , GRCh38.p12 chr8: 208,049-11,108,117	CLDN23, HSPD1P3, 270 more genes
nsv3902717	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-10,939,681 , GRCh38.p12 chr8: 208,048-11,082,171 , GRCh38.p12 chr8\|NW_018654717.1: 1-5,513,617	CLDN23, LOC101929128, 270 more genes
nsv3921576	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,530-10,724,642 , GRCh38 chr8: 241,530-10,867,132 , NCBI36 chr8: 181,530-10,762,052	CLDN23, SPAG11B, 213 more genes
nsv3900231	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 10,213-10,197,718 , GRCh38.p12 chr8\|NW_018654717.1: 1-5,513,617 , GRCh38.p12 chr8: 60,213-10,340,208	CLDN23, LOC105377793, 273 more genes
nsv3911012	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,530-10,315,994 , GRCh38 chr8: 241,530-10,458,484 , NCBI36 chr8: 181,530-10,353,404	CLDN23, DEFB4A, 197 more genes
nsv3912676	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 241,530-10,191,595 , NCBI36 chr8: 181,530-10,086,515 , GRCh37 chr8: 191,530-10,049,105	CLDN23, FAM90A23, 196 more genes
nsv3900485	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 164,984-10,007,227 , GRCh38.p12 chr8: 214,984-10,149,717	CLDN23, RNA5SP251, 197 more genes
nsv3903778	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-9,749,574 , GRCh38.p12 chr8: 208,048-9,892,064	CLDN23, LOC105379230, 193 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 128

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Number of Variants: 20

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