mia[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
nsv6289994	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 44,559,541-44,571,008 , GRCh38.p12 chr2: 44,332,402-44,343,869	PREPL
nsv1397893	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr15: 56,918,090-57,291,261 , GRCh37 chr15: 57,210,288-57,583,459	TCF12, LOC145783, 2 more genes
nsv3895898	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 41,282,275-41,284,240 , GRCh38.p12 chr19: 40,776,370-40,778,335	MIA, RAB4B, 2 more genes
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	H3P40, EEF1B2P1, 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	RNU6-18P, GOLGA8K, 1442 more genes
nsv3903255	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 41,689,327-52,446,981 , GRCh38.p12 chr15: 41,397,129-52,154,784	RN7SKP101, SQOR, 234 more genes
nsv3903669	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 43,759,773-53,252,240 , GRCh38.p12 chr15: 43,467,575-52,960,043	MIR4712, HYPK, 188 more genes
nsv3902367	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 42,850,434-49,592,633 , GRCh38.p12 chr15: 42,558,236-49,300,436	SERF2-C15ORF63, TGM7, 142 more genes
nsv6290201	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 43,851,199-44,038,820 , GRCh38.p12 chr15: 43,559,001-43,746,622	CATSPER2P1, CKMT1A, 13 more genes
nsv6290131	copy number variation	2	nstd102	human	Pathogenic, Likely pathogenic	GRCh37 chr15: 43,851,199-44,038,794 , GRCh38.p12 chr15: 43,559,001-43,746,596	STRCP1, CKMT1B, 13 more genes
nsv3906590	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 43,868,571-44,014,518 , GRCh38.p12 chr15: 43,576,373-43,722,320	CKMT1B, PPIP5K1P1-CATSPER2, 10 more genes
nsv3872983	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 43,594,659-43,700,429 , GRCh37 chr15: 43,886,857-43,992,627	CKMT1A, CATSPER2, 9 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	MYZAP, JMJD7, 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	MIR4513, LOC727751, 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	TMEM202, SNORD115-28, 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	FES, OR4H6BP, 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	FAM81A, LOC105370884, 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	RNU6-953P, LOC105370805, 1385 more genes
nsv3899559	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 41,745,084-102,354,798 , GRCh38.p12 chr15: 41,452,886-101,814,595	CILP, HDDC3, 1176 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	MIA, ZNF321P, 2443 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 55

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Number of Variants: 20

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