commd3[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
nsv3905655	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 22,603,581-22,639,707 , GRCh38.p12 chr10: 22,314,652-22,350,778	COMMD3, BMI1, 2 more genes
nsv3907360	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 22,597,174-22,679,177 , GRCh38.p12 chr10: 22,308,245-22,390,248	COMMD3, COMMD3-BMI1, 2 more genes
nsv3890692	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 22,601,976-22,675,857 , GRCh38.p12 chr10: 22,313,047-22,386,928	COMMD3, COMMD3-BMI1, 2 more genes
nsv3908588	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 22,594,765-22,639,707 , GRCh38.p12 chr10: 22,305,836-22,350,778	COMMD3, SPAG6, 2 more genes
nsv3906141	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 22,594,765-22,637,381 , GRCh38.p12 chr10: 22,305,836-22,348,452	COMMD3, SPAG6, 2 more genes
nsv3907107	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 22,597,174-22,637,381 , GRCh38.p12 chr10: 22,308,245-22,348,452	COMMD3, COMMD3-BMI1, 2 more genes
nsv3908299	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 22,601,976-22,639,707 , GRCh38.p12 chr10: 22,313,047-22,350,778	COMMD3, COMMD3-BMI1, 2 more genes
nsv3895110	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 22,601,976-22,637,381 , GRCh38.p12 chr10: 22,313,047-22,348,452	COMMD3, COMMD3-BMI1, 2 more genes
nsv3904392	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 22,603,581-22,637,381 , GRCh38.p12 chr10: 22,314,652-22,348,452	COMMD3, COMMD3-BMI1, 2 more genes
nsv3899582	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 22,607,432-22,637,381 , GRCh38.p12 chr10: 22,318,503-22,348,452	COMMD3, COMMD3-BMI1, 2 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	COMMD3, RNU7-12P, 1876 more genes
nsv3906389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996	COMMD3, LOC100419870, 2105 more genes
nsv3891157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558	COMMD3, AGAP14P, 2097 more genes
nsv3902271	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639	COMMD3, ANXA11, 2085 more genes
nsv3891958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414	COMMD3, TUBB8, 2085 more genes
nsv7137211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639	COMMD3, EXOC6, 1906 more genes
nsv3904390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 100,026-50,961,640 , GRCh38.p12 chr10: 54,086-49,753,594	COMMD3, LINC00700, 806 more genes
nsv3920796	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 62,842-35,729,127 , GRCh37.p13 chr10: 72,842-35,689,121 , GRCh38.p12 chr10: 26,906-35,400,193	COMMD3, EPC1-AS1, 559 more genes
nsv6313952	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593	COMMD3, RPL36AP55, 418 more genes
nsv3917667	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 224,406-26,628,907 , GRCh38 chr10: 90,205-26,339,978 , NCBI36 chr10: 126,145-26,668,913	COMMD3, RN7SKP241, 389 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 29

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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