dcdc1[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
nsv3899136	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 31,311,902-31,349,768 , GRCh38.p12 chr11: 31,290,355-31,328,221	DCDC1
nsv3896238	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 31,312,348-31,345,582 , GRCh38.p12 chr11: 31,290,801-31,324,035	DCDC1
nsv4456701	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 30,956,147-31,048,683 , GRCh38.p12 chr11: 30,934,600-31,027,136	DCDC1
nsv3899578	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr11: 31,292,909-31,357,084 , GRCh38.p12 chr11: 31,271,362-31,335,537	DCDC1, CYCSP25
nsv3904057	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 31,390,733-31,414,949 , GRCh38.p12 chr11: 31,369,186-31,393,402	DCDC1, DNAJC24
nsv3905337	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 31,385,819-31,397,428 , GRCh38.p12 chr11: 31,364,272-31,375,881	DCDC1, DNAJC24
nsv3907243	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 31,389,267-31,397,428 , GRCh38.p12 chr11: 31,367,720-31,375,881	DCDC1, DNAJC24
nsv3904510	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 31,210,842-31,312,348 , GRCh38.p12 chr11: 31,189,295-31,290,801	DCDC1, CYCSP25
nsv4457300	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 31,326,349-31,415,981 , GRCh38.p12 chr11: 31,304,802-31,394,434	DCDC1, DNAJC24
nsv3876220	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 30,967,000-31,704,000 , GRCh37 chr11: 31,010,424-31,747,424 , GRCh38 chr11: 30,988,877-31,725,876	DCDC1, CYCSP25, 3 more genes
nsv3907686	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 31,083,877-31,704,548 , GRCh38.p12 chr11: 31,062,330-31,683,000	DCDC1, ELP4, 3 more genes
nsv3892283	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 31,147,306-31,714,853 , GRCh38.p12 chr11: 31,125,759-31,693,305	DCDC1, CYCSP25, 3 more genes
nsv3886288	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 31,108,579-31,649,842 , GRCh37 chr11: 31,152,003-31,693,266 , GRCh38 chr11: 31,130,456-31,671,718	DCDC1, CYCSP25, 3 more genes
nsv3880865	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 31,234,395-31,751,815 , GRCh37 chr11: 31,277,819-31,795,239 , GRCh38 chr11: 31,256,273-31,773,692	DCDC1, ELP4, 3 more genes
nsv3916469	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 31,167,418-31,679,257 , GRCh37 chr11: 31,210,842-31,722,681 , GRCh38 chr11: 31,189,295-31,701,133	DCDC1, CYCSP25, 3 more genes
nsv3895517	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 31,186,493-31,698,208 , GRCh38.p12 chr11: 31,164,946-31,676,660	DCDC1, DNAJC24, 3 more genes
nsv3912592	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 31,277,446-31,768,195 , GRCh37 chr11: 31,320,870-31,811,619 , GRCh38 chr11: 31,299,323-31,790,071	DCDC1, PAX6, 3 more genes
nsv3922319	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 31,092,182-31,556,821 , NCBI36 chr11: 31,048,758-31,513,397 , GRCh38 chr11: 31,070,635-31,535,274	DCDC1, IMMP1L, 3 more genes
nsv3919093	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr11: 31,277,446-31,704,207 , GRCh38 chr11: 31,299,323-31,726,083 , GRCh37 chr11: 31,320,870-31,747,631	DCDC1, DNAJC24, 2 more genes
nsv7093683	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 31,284,610-31,671,789 , GRCh38.p12 chr11: 31,263,063-31,650,241	DCDC1, DNAJC24, 3 more genes

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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

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Items: 1 to 20 of 63

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Number of Variants: 20

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