acbd5[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
nsv4685701	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 27,504,464-27,504,571 , GRCh38.p12 chr10: 27,215,535-27,215,642	ACBD5
nsv4685785	delins	1	nstd102	human	Likely pathogenic	GRCh38 chr10: 27,216,906-27,217,979 , GRCh37 chr10: 27,505,835-27,506,908	ACBD5
nsv5564285	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 27,494,107-27,494,197 , GRCh38.p12 chr10: 27,205,178-27,205,268	ACBD5
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	ACBD5, RNU7-12P, 1876 more genes
nsv3911283	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 27,111,945-30,537,855 , NCBI36 chr10: 27,151,951-30,577,861 , GRCh38 chr10: 26,823,016-30,248,926	ACBD5, YME1L1, 72 more genes
nsv3915584	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 27,046,685-30,228,891 , GRCh37 chr10: 27,335,614-30,517,820 , NCBI36 chr10: 27,375,620-30,557,826	ACBD5, TRIAP1P1, 70 more genes
nsv6291211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 27,204,530-29,105,882 , GRCh38.p12 chr10: 26,915,601-28,816,953	ACBD5, LINC02673, 44 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	ACBD5, 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	ACBD5, 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	ACBD5, 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	ACBD5, 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	ACBD5, 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	ACBD5, 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	ACBD5, 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	ACBD5, RPL36AP55, 418 more genes
nsv3911634	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr10: 19,417,096-33,061,227 , GRCh37 chr10: 19,377,090-33,021,221 , GRCh38 chr10: 19,088,161-32,732,293	ACBD5, BMI1, 221 more genes
nsv3905128	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 27,266,501-27,723,033 , GRCh38.p12 chr10: 26,977,572-27,434,104	ACBD5, RNU6-666P, 14 more genes
nsv3920598	copy number variation	1	nstd102	human	Benign	NCBI36 chr10: 4,636,926-47,125,152 , GRCh38 chr10: 4,604,734-48,074,662 , GRCh37 chr10: 4,646,926-47,531,169	ACBD5, LOC100420467, 709 more genes
nsv3891361	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr10: 26,318,337-27,889,818 , GRCh38.p12 chr10: 26,029,408-27,600,889	ACBD5, ABI1, 31 more genes
nsv3898766	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr10: 26,344,939-27,889,818 , GRCh38.p12 chr10: 26,056,010-27,600,889	ACBD5, RNU6-490P, 31 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 26

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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