znf280d[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	ZNF280D, 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	ZNF280D, RNU6-18P, 1442 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	ZNF280D, LOC112268148, 131 more genes
nsv3899878	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 54,713,558-62,769,295 , GRCh38.p12 chr15: 54,421,360-62,477,096	ZNF280D, RAB27A, 120 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	ZNF280D, MAPK6-DT, 76 more genes
nsv6291481	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 55,772,371-57,880,518 , GRCh38.p12 chr15: 55,480,173-57,588,320	ZNF280D, PRTG, 27 more genes
nsv7094391	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 56,961,021-57,839,688 , GRCh38.p12 chr15: 56,668,823-57,547,490	ZNF280D, LOC107984759, 11 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	ZNF280D, 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	ZNF280D, 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	ZNF280D, 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	ZNF280D, 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	ZNF280D, 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	ZNF280D, RNU6-953P, 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	ZNF280D, CILP, 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	ZNF280D, LINC03065, 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	ZNF280D, MIR1266, 199 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	ZNF280D, DMXL2, 91 more genes
nsv3918770	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189	ZNF280D, SNRPCP18, 1622 more genes
nsv3918644	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189	ZNF280D, SNORD116-23, 1622 more genes
nsv3911945	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 20,203,424-100,338,915 , GRCh37.p13 chr15: 22,652,060-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189	ZNF280D, HDDC3, 1622 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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