c22orf23[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
nsv3892611	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 38,337,934-38,343,443 , GRCh38.p12 chr22: 37,941,927-37,947,436	C22ORF23, MICALL1
nsv3922128	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 35,729,986-39,296,182 , NCBI36 chr22: 34,059,986-37,626,128 , GRCh38 chr22: 35,333,993-38,900,177	C22ORF23, LOC102724378, 120 more genes
nsv7095836	copy number variation	3	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr22: 37,154,355-39,148,633 , GRCh38.p12 chr22: 36,758,311-38,752,628	C22ORF23, CSF2RBP1, 80 more genes
nsv3904443	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 36,877,226-38,548,989 , GRCh38.p12 chr22: 36,481,179-38,152,982	C22ORF23, LOC107985576, 63 more genes
nsv3915039	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 37,447,222-39,103,680 , GRCh37 chr22: 37,843,259-39,499,685 , NCBI36 chr22: 36,173,205-37,829,631	C22ORF23, MIR4534, 68 more genes
nsv7096310	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 38,097,373-39,306,081 , GRCh38.p12 chr22: 37,701,366-38,910,076	C22ORF23, TMEM184B, 46 more genes
nsv3892449	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 37,866,631-39,054,815 , GRCh38.p12 chr22: 37,470,593-38,658,810	C22ORF23, MIR658, 48 more genes
nsv3913000	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 38,117,784-39,282,669 , GRCh38 chr22: 37,721,777-38,886,664 , NCBI36 chr22: 36,447,730-37,612,615	C22ORF23, DDX17, 46 more genes
nsv4676116	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 38,002,218-38,973,070 , GRCh38.p12 chr22: 37,606,211-38,577,065	C22ORF23, CSNK1E, 43 more genes
nsv5200376	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 38,155,164-38,541,997 , GRCh38.p12 chr22: 37,759,157-38,145,990	C22ORF23, H1-0, 18 more genes
nsv3918848	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 37,805,546-37,983,784 , GRCh37 chr22: 38,201,553-38,379,791	C22ORF23, MIR6820, 11 more genes
nsv3902776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,667-51,243,435 , GRCh38.p12 chr22: 16,367,190-50,805,007	C22ORF23, LOC100419811, 1084 more genes
nsv3894026	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,237,518 , GRCh38.p12 chr22: 16,367,190-50,799,090	C22ORF23, IGKV3OR22-2, 1084 more genes
nsv3890411	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,237,463 , GRCh38.p12 chr22: 16,367,190-50,799,035	C22ORF23, RNU6-495P, 1084 more genes
nsv4729926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824	C22ORF23, FBXO7, 1084 more genes
nsv3902598	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,220,902 , GRCh38.p12 chr22: 16,367,190-50,782,474	C22ORF23, FABP5P11, 1084 more genes
nsv3907231	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,114,244-51,211,392 , GRCh38.p12 chr22: 16,367,190-50,772,964	C22ORF23, DDTL, 1084 more genes
nsv3890401	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,114,244-51,195,728 , GRCh38.p12 chr22: 16,367,190-50,757,300	C22ORF23, YPEL1, 1083 more genes
nsv4457771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410	C22ORF23, IGLV3-27, 1082 more genes
nsv3891895	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,900-51,197,838 , GRCh38.p12 chr22: 16,408,174-50,759,410	C22ORF23, POM121L7P, 1082 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 31

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Number of Variants: 20

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Supplemental Content

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