cacnb2[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
nsv3906419	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 18,550,958-18,592,873 , GRCh38.p12 chr10: 18,262,029-18,303,944	CACNB2
nsv3903876	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 18,550,958-18,583,866 , GRCh38.p12 chr10: 18,262,029-18,294,937	CACNB2
nsv7093870	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 18,629,856-18,629,926 , GRCh38.p12 chr10: 18,340,927-18,340,997	CACNB2
nsv3892787	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 18,825,694-18,868,070 , GRCh38.p12 chr10: 18,536,765-18,579,141	CACNB2, NSUN6
nsv4456407	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 18,765,120-18,890,374 , GRCh38.p12 chr10: 18,476,191-18,601,445	CACNB2, NSUN6
nsv3894213	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 18,794,238-18,834,881 , GRCh38.p12 chr10: 18,505,309-18,545,952	CACNB2, NSUN6
nsv5380865	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 18,795,390-18,828,653 , GRCh38.p12 chr10: 18,506,461-18,539,724	CACNB2, NSUN6
nsv7093787	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 18,807,245-18,828,653 , GRCh38.p12 chr10: 18,518,316-18,539,724	CACNB2, NSUN6
nsv4682854	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 18,807,255-18,828,663 , GRCh38.p12 chr10: 18,518,326-18,539,734	CACNB2, NSUN6
nsv6314268	insertion	1	nstd102	human	Uncertain significance	GRCh38 chr10: 18,539,723-18,539,723 , GRCh37 chr10: 18,828,652-18,828,652	CACNB2, NSUN6
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	CACNB2, RNU7-12P, 1876 more genes
nsv3914771	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 54,086-19,336,980 , NCBI36 chr10: 90,026-19,665,915 , GRCh37 chr10: 100,026-19,625,909	CACNB2, COX6CP17, 302 more genes
nsv3884983	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 4,689,760-19,120,882 , GRCh38.p12 chr10: 4,647,568-18,831,953	CACNB2, HSPA14, 228 more genes
nsv3911783	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 7,510,738-21,916,687 , GRCh37 chr10: 7,470,732-21,876,681 , GRCh38 chr10: 7,428,770-21,587,752	CACNB2, LOC101928834, 192 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	CACNB2, 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	CACNB2, 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	CACNB2, 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	CACNB2, 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	CACNB2, 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	CACNB2, LINC00700, 806 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 35

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Number of Variants: 20

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Supplemental Content

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