minar1[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
nsv3892725	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 79,731,046-79,740,689 , GRCh38.p12 chr15: 79,438,704-79,448,347	MINAR1
nsv3900102	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 79,731,069-79,740,689 , GRCh38.p12 chr15: 79,438,727-79,448,347	MINAR1
nsv3904292	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 79,731,120-79,740,689 , GRCh38.p12 chr15: 79,438,778-79,448,347	MINAR1
nsv3895718	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 79,729,877-79,736,482 , GRCh38.p12 chr15: 79,437,535-79,444,140	MINAR1
nsv3900802	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 79,731,046-79,736,482 , GRCh38.p12 chr15: 79,438,704-79,444,140	MINAR1
nsv3904676	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 79,731,120-79,736,482 , GRCh38.p12 chr15: 79,438,778-79,444,140	MINAR1
nsv3894990	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 79,729,877-79,732,217 , GRCh38.p12 chr15: 79,437,535-79,439,875	MINAR1
nsv3895489	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 79,729,997-79,732,217 , GRCh38.p12 chr15: 79,437,655-79,439,875	MINAR1
nsv3892640	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 79,731,069-79,732,217 , GRCh38.p12 chr15: 79,438,727-79,439,875	MINAR1
nsv3891552	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 79,730,110-79,731,428 , GRCh38.p12 chr15: 79,437,768-79,439,086	MINAR1
nsv4674907	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 79,635,680-79,742,970 , GRCh38.p12 chr15: 79,343,338-79,450,628	MINAR1, TMED3
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	MINAR1, H3P40, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	MINAR1, RNU6-18P, 1442 more genes
nsv3913830	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 76,006,154-79,982,417 , NCBI36 chr15: 74,085,550-78,061,814 , GRCh37 chr15: 76,298,495-80,274,759	MINAR1, TSPAN3, 86 more genes
nsv3900281	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337	MINAR1, MYZAP, 1750 more genes
nsv3913581	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189	MINAR1, MIR4513, 1754 more genes
nsv3904086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959	MINAR1, TMEM202, 1747 more genes
nsv3905138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413	MINAR1, FES, 1738 more genes
nsv3892955	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909	MINAR1, FAM81A, 1614 more genes
nsv3876912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654	MINAR1, RNU6-953P, 1385 more genes

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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 43

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Number of Variants: 20

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Supplemental Content

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