hnf6[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
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
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
nsv6313917	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 47,635,238-56,509,908 , GRCh38.p12 chr15: 47,343,041-56,217,710	PYGO1, RNU6-449P, 125 more genes
nsv3913164	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 50,864,913-59,646,577 , GRCh37 chr15: 51,157,110-59,938,776 , NCBI36 chr15: 48,944,402-57,726,068	LOC112268148, MTND4LP23, 131 more genes
nsv3910893	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 49,356,179-55,167,876 , GRCh37 chr15: 51,568,887-57,380,584 , GRCh38 chr15: 51,276,690-57,088,386	MAPK6-DT, MAPK6, 76 more genes
nsv4769387	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 48,744,917-53,851,050 , GRCh38.p12 chr15: 48,452,720-53,558,853	BCL2L10, RNA5SP394, 86 more genes
nsv7094385	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr15: 50,999,997-54,025,330 , GRCh38.p12 chr15: 50,707,800-53,733,133	LOC105370826, MIR7973-2, 48 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
nsv6637384	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239	LINC03065, FAM227B, 228 more genes
nsv4456196	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 48,000,433-60,747,551 , GRCh38.p12 chr15: 47,708,236-60,455,352	MIR1266, AQP9, 199 more genes
nsv4455359	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 49,031,132-56,740,397 , GRCh38.p12 chr15: 48,738,935-56,448,199	MIR4716, RPS13P8, 112 more genes
nsv3893150	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 50,727,285-57,603,305 , GRCh38.p12 chr15: 50,435,088-57,311,107	DMXL2, MYO5C, 91 more genes
nsv4729282	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr15: 51,792,729-55,134,365 , GRCh38.p12 chr15: 51,500,532-54,842,167	EEF1B2P1, ONECUT1, 41 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 30

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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