ascc1[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
nsv6290217	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,887,840-73,921,432 , GRCh38 chr10: 72,128,082-72,161,674	ASCC1
nsv7098848	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 72,138,925-72,163,147 , GRCh37.p13 chr10: 73,898,683-73,922,905	ASCC1
nsv6137656	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,970,434-73,973,122 , GRCh38.p12 chr10: 72,210,676-72,213,364	ASCC1
nsv6309163	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,970,470-73,973,056 , GRCh38.p12 chr10: 72,210,712-72,213,298	ASCC1
nsv7093893	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,970,470-73,970,609 , GRCh38.p12 chr10: 72,210,712-72,210,851	ASCC1
nsv7093190	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr10: 72,210,847-72,210,848 , GRCh37 chr10: 73,970,605-73,970,606	ASCC1
nsv6309008	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 73,862,127-73,862,745 , GRCh38.p12 chr10: 72,102,369-72,102,987	ASCC1
nsv3890371	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 73,908,208-73,949,708 , GRCh38.p12 chr10: 72,148,450-72,189,950	ASCC1, RPL15P14
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	ASCC1, RNU7-12P, 1876 more genes
nsv3922335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 60,196,226-76,174,974 , GRCh38 chr10: 58,436,466-74,415,216 , NCBI36 chr10: 59,866,232-75,844,980	ASCC1, UNC5B-AS1, 250 more genes
nsv3917822	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 63,402,579-75,296,099 , GRCh37 chr10: 65,162,339-77,055,857 , NCBI36 chr10: 64,832,345-76,725,863	ASCC1, MYL6P3, 220 more genes
nsv6314185	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956	ASCC1, SLC25A16, 204 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	ASCC1, 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	ASCC1, 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	ASCC1, 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	ASCC1, 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	ASCC1, EXOC6, 1906 more genes
nsv3924859	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961	ASCC1, BMS1P4-AGAP5, 471 more genes
nsv3917047	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 42,500,760-75,145,672 , GRCh37 chr10: 43,180,754-75,475,666 , GRCh38 chr10: 42,685,306-73,715,908	ASCC1, SLC9A3P3, 476 more genes
nsv3891070	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 69,040,366-93,194,993 , GRCh38.p12 chr10: 67,280,608-91,435,236	ASCC1, NRG3-AS1, 441 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 23

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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