dcun1d1[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
nsv3880195	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 182,530,969-182,703,096 , GRCh38.p12 chr3: 182,813,181-182,985,308	DCUN1D1, LOC105374246, 3 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	DCUN1D1, SNORA4, 199 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	DCUN1D1, VPS8, 171 more genes
nsv6313539	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,189,525-187,212,935 , GRCh38.p12 chr3: 182,471,737-187,495,147	DCUN1D1, ALG3, 133 more genes
nsv6634384	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 181,062,175-185,474,509 , GRCh38.p12 chr3: 181,344,387-185,756,721	DCUN1D1, PRICKLE1P1, 99 more genes
nsv4769252	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 181,171,210-184,706,091 , GRCh38.p12 chr3: 181,453,422-184,988,303	DCUN1D1, LOC107986054, 83 more genes
nsv4769308	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 180,834,336-183,551,661 , GRCh38.p12 chr3: 181,116,548-183,833,873	DCUN1D1, SNORD3P4, 43 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	DCUN1D1, 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	DCUN1D1, 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	DCUN1D1, 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	DCUN1D1, 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	DCUN1D1, 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	DCUN1D1, 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	DCUN1D1, LOC105374260, 696 more genes
nsv3918149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 155,836,230-197,851,986 , GRCh38 chr3: 156,118,441-198,125,115 , NCBI36 chr3: 157,318,924-199,336,383	DCUN1D1, LINC02031, 647 more genes
nsv3913128	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 156,321,878-198,113,452 , NCBI36 chr3: 157,522,361-199,324,720 , GRCh37 chr3: 156,039,667-197,840,323	DCUN1D1, SNORA4, 644 more genes
nsv3914686	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 158,493,861-199,345,995 , GRCh37 chr3: 157,011,167-197,861,598 , GRCh38 chr3: 157,293,378-198,134,727	DCUN1D1, RPL34P10, 625 more genes
nsv3871065	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 158,980,631-197,766,890 , GRCh38.p12 chr3: 159,262,842-198,040,019	DCUN1D1, LINC02048, 599 more genes
nsv3912173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 167,337,691-199,336,383 , GRCh37 chr3: 165,854,997-197,851,986 , GRCh38 chr3: 166,137,209-198,125,115	DCUN1D1, LOC105374277, 540 more genes
nsv3918982	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 167,885,356-197,837,049 , NCBI36 chr3: 169,368,050-199,321,446 , GRCh38 chr3: 168,167,568-198,110,178	DCUN1D1, EIF4G1, 515 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 33

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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