mccc1[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
nsv7096453	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,769,927-182,817,228 , GRCh38.p12 chr3: 183,052,139-183,099,440	MCCC1
nsv6311865	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,790,144-182,817,385 , GRCh38.p12 chr3: 183,072,356-183,099,597	MCCC1
nsv7096950	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,754,986-182,775,230 , GRCh38.p12 chr3: 183,037,198-183,057,442	MCCC1
nsv7096554	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,754,986-182,770,048 , GRCh38.p12 chr3: 183,037,198-183,052,260	MCCC1
nsv7096452	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,756,794-182,763,348 , GRCh38.p12 chr3: 183,039,006-183,045,560	MCCC1
nsv4681460	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,788,777-182,790,285 , GRCh38.p12 chr3: 183,070,989-183,072,497	MCCC1
nsv7098855	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,759,355-182,759,538 , GRCh38.p12 chr3: 183,041,567-183,041,750	MCCC1
nsv4682300	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,810,177-182,810,353 , GRCh38.p12 chr3: 183,092,389-183,092,565	MCCC1
nsv5673720	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,733,206-182,733,374 , GRCh38.p12 chr3: 183,015,418-183,015,586	MCCC1
nsv4450808	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,769,927-182,770,048 , GRCh38 chr3: 183,052,139-183,052,260	MCCC1
nsv5673476	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,817,140-182,817,228 , GRCh38.p12 chr3: 183,099,352-183,099,440	MCCC1
nsv4683140	copy number variation	2	nstd102	human	Pathogenic, Likely pathogenic	GRCh37 chr3: 182,810,187-182,812,403 , GRCh38.p12 chr3: 183,092,399-183,094,615	MCCC1
nsv3887837	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 182,737,878-182,814,840 , GRCh38.p12 chr3: 183,020,090-183,097,052	MCCC1
nsv3881342	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 182,746,355-182,804,565 , GRCh38.p12 chr3: 183,028,567-183,086,777	MCCC1
nsv6311785	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 182,733,226-182,817,228 , GRCh38.p12 chr3: 183,015,438-183,099,440	MCCC1
nsv7093524	insertion	1	nstd102	human	Uncertain significance	GRCh37 chr3: 182,788,979-182,788,979 , GRCh38 chr3: 183,071,191-183,071,191	MCCC1
nsv4452071	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 182,787,792-182,922,112 , GRCh38.p12 chr3: 183,070,004-183,204,324	MCCC1, MCF2L2, 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	MCCC1, 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	MCCC1, 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	MCCC1, ALG3, 133 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

Search results

Items: 1 to 20 of 50

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Number of Variants: 20

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Supplemental Content

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