znf423[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
nsv3905247	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 49,889,523-49,898,706 , GRCh38.p12 chr16: 49,855,612-49,864,795	ZNF423
nsv3900655	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 49,889,115-49,898,755 , GRCh38.p12 chr16: 49,855,204-49,864,844	ZNF423
nsv5564383	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr16: 49,635,768-49,635,847 , GRCh37 chr16: 49,669,679-49,669,758	ZNF423
nsv7094845	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 49,823,378-49,856,596 , GRCh38.p12 chr16: 49,789,467-49,822,685	ZNF423
nsv3892732	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 49,796,534-49,837,475 , GRCh38.p12 chr16: 49,762,623-49,803,564	ZNF423, MRPS21P8
nsv3922538	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr16: 48,347,151-48,500,025 , GRCh37.p13 chr16: 49,789,650-49,942,524 , GRCh38.p12 chr16: 49,755,739-49,908,613	ZNF423, MRPS21P8
nsv3912665	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 45,842,056-52,712,889 , GRCh37 chr16: 47,284,555-54,155,388 , GRCh38 chr16: 47,250,644-54,121,476	ZNF423, RPL10P14, 110 more genes
nsv3910120	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 46,500,741-52,456,082 , NCBI36 chr16: 45,058,242-51,013,583 , GRCh38 chr16: 46,466,829-52,422,170	ZNF423, CYLD-AS1, 103 more genes
nsv3915496	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 46,505,432-52,439,868 , GRCh38 chr16: 46,471,520-52,405,956 , NCBI36 chr16: 45,062,933-50,997,369	ZNF423, SNORD148, 102 more genes
nsv3914752	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 46,500,741-51,973,216 , GRCh38 chr16: 46,466,829-51,939,304 , NCBI36 chr16: 45,058,242-50,530,717	ZNF423, CNEP1R1, 94 more genes
nsv3920484	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 46,466,829-51,673,196 , GRCh37 chr16: 46,500,741-51,707,107 , NCBI36 chr16: 45,058,242-50,264,608	ZNF423, NETO2, 92 more genes
nsv3903769	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 46,737,110-51,838,691 , GRCh38.p12 chr16: 46,703,198-51,804,780	ZNF423, N4BP1, 86 more genes
nsv3917177	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 49,570,553-53,467,065 , NCBI36 chr16: 48,161,965-52,058,478 , GRCh37 chr16: 49,604,464-53,500,977	ZNF423, LOC107984901, 66 more genes
nsv3917348	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 48,332,219-50,468,032 , GRCh37 chr16: 49,774,718-51,910,531 , GRCh38 chr16: 49,740,807-51,876,620	ZNF423, NOD2, 38 more genes
nsv3906108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224	ZNF423, CKLF, 1882 more genes
nsv3904593	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973	ZNF423, LOC100128079, 1879 more genes
nsv3901410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287	ZNF423, LINC02175, 1877 more genes
nsv3909417	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867	ZNF423, PRSS53, 1868 more genes
nsv3892266	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654	ZNF423, FTLP14, 1868 more genes
nsv3921269	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345	ZNF423, LOC105371237, 985 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 43

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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