dlg5[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
nsv3900400	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 79,685,769-79,686,700 , GRCh38.p12 chr10\|NT_187580.1: 164,703-165,634 , GRCh38.p12 chr10: 77,926,011-77,926,942	DLG5, DLG5-AS1
nsv3901114	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 79,685,795-79,686,700 , GRCh38.p12 chr10\|NT_187580.1: 164,729-165,634 , GRCh38.p12 chr10: 77,926,037-77,926,942	DLG5, DLG5-AS1
nsv3896932	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 79,685,769-79,686,387 , GRCh38.p12 chr10: 77,926,011-77,926,629 , GRCh38.p12 chr10\|NT_187580.1: 164,703-165,321	DLG5, DLG5-AS1
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	DLG5, 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	DLG5, 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	DLG5, 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	DLG5, 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	DLG5, 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	DLG5, 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	DLG5, BMS1P4-AGAP5, 471 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	DLG5, NRG3-AS1, 441 more genes
nsv3917966	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 68,626,331-80,851,819 , GRCh37 chr10: 68,956,325-81,181,813 , GRCh38 chr10: 67,196,567-79,422,057	DLG5, LINC02640, 231 more genes
nsv4729169	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr10: 79,356,214-79,614,826 , GRCh38.p12 chr10: 77,596,456-77,855,068	DLG5, KCNMA1, 5 more genes
nsv3921041	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr10: 79,044,314-79,281,573 , GRCh37 chr10: 79,374,308-79,611,567 , GRCh38 chr10: 77,614,550-77,851,809	DLG5, IMPDH1P5, 5 more genes
nsv3908876	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr10: 79,361,273-79,576,985 , GRCh38.p12 chr10: 77,601,515-77,817,227	DLG5, LOC105378372, 5 more genes
nsv3907664	copy number variation	1	nstd102	human	drug response	GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422	DLG5, SHOC2, 1487 more genes
nsv3913031	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 79,551,056-79,837,705 , NCBI36 chr10: 79,221,062-79,507,711 , GRCh38 chr10: 77,791,298-78,077,947	DLG5, POLR3A, 6 more genes
nsv3873639	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr10: 79,036,437-79,286,611 , GRCh37.p13 chr10: 79,366,431-79,616,605 , GRCh38.p12 chr10: 77,606,673-77,856,847	DLG5, LOC399783, 5 more genes
nsv7093652	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 79,397,003-79,603,484 , GRCh38.p12 chr10: 77,637,245-77,843,726	DLG5, LOC105378372, 5 more genes
nsv7093801	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 75,671,314-79,799,964 , GRCh38.p12 chr10: 73,911,556-78,040,206	DLG5, COMTD1, 53 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 22

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Number of Variants: 20

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Supplemental Content

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Search details

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