mcmbp[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
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	MCMBP, RNU7-12P, 1876 more genes
nsv3920295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422	MCMBP, EIF2S2P3, 895 more genes
nsv6314129	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 117,019,650-125,217,066 , GRCh38.p12 chr10: 115,260,173-123,457,550	MCMBP, PDZD8, 122 more genes
nsv4349508	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 117,024,753-124,942,806 , GRCh38.p12 chr10: 115,265,276-123,183,290	MCMBP, PRLHR, 121 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	MCMBP, 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	MCMBP, 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	MCMBP, 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	MCMBP, 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	MCMBP, EXOC6, 1906 more genes
nsv3905489	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,283,493-135,427,143 , GRCh38.p12 chr10: 91,523,736-133,613,639	MCMBP, LOC105378476, 688 more genes
nsv3890046	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 94,346,520-135,427,143 , GRCh38.p12 chr10: 92,586,763-133,613,639	MCMBP, UROS, 667 more genes
nsv3921919	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 100,600,492-133,622,588 , GRCh37 chr10: 102,360,249-135,436,092 , NCBI36 chr10: 102,350,239-135,286,082	MCMBP, MIR4295, 508 more genes
nsv3898332	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 103,288,313-135,512,075 , GRCh38.p12 chr10: 101,528,556-133,774,750	MCMBP, NPS, 503 more genes
nsv3923769	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291	MCMBP, LOC105378493, 477 more genes
nsv3903027	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 105,613,040-135,427,143 , GRCh38.p12 chr10: 103,853,282-133,613,639	MCMBP, YWHAZP5, 415 more genes
nsv3908254	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 106,003,533-135,427,143 , GRCh38.p12 chr10: 104,243,775-133,613,639	MCMBP, MIR4680, 404 more genes
nsv6314085	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639	MCMBP, LOC107984268, 379 more genes
nsv3912079	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 109,852,335-135,284,168 , GRCh38 chr10: 108,102,587-133,620,674 , GRCh37 chr10: 109,862,345-135,434,178	MCMBP, TUBGCP2, 372 more genes
nsv4348764	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 110,022,170-135,439,095 , GRCh38.p12 chr10: 108,262,412-133,625,591	MCMBP, LOC105378492, 373 more genes
nsv3923859	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 113,062,847-135,284,168 , GRCh37 chr10: 113,072,857-135,434,178 , GRCh38 chr10: 111,313,099-133,620,674	MCMBP, AS-PTPRE, 330 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 38

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Number of Variants: 20

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Supplemental Content

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Search details

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