dnaaf4[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
nsv7094299	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 55,783,301-55,790,527 , GRCh38.p12 chr15: 55,491,103-55,498,329	DNAAF4, DNAAF4-CCPG1
nsv4768348	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 55,429,622-55,432,751 , GRCh37 chr15: 55,721,820-55,724,949	DNAAF4, DNAAF4-CCPG1
nsv3871988	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 55,430,650-55,432,622 , GRCh37 chr15: 55,722,848-55,724,820	DNAAF4, DNAAF4-CCPG1
nsv7094389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 55,722,868-55,724,820 , GRCh38.p12 chr15: 55,430,670-55,432,622	DNAAF4, DNAAF4-CCPG1
nsv4453901	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr15: 55,430,664-55,432,608 , GRCh37 chr15: 55,722,862-55,724,806	DNAAF4, DNAAF4-CCPG1
nsv7094390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 55,789,890-55,790,527 , GRCh38.p12 chr15: 55,497,692-55,498,329	DNAAF4, DNAAF4-CCPG1
nsv5672586	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 55,731,650-55,731,799 , GRCh38.p12 chr15: 55,439,452-55,439,601	DNAAF4, DNAAF4-CCPG1
nsv3880335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 55,742,420-55,742,565 , GRCh38 chr15: 55,450,222-55,450,367	DNAAF4, DNAAF4-CCPG1
nsv7099025	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 55,731,670-55,731,779 , GRCh38 chr15: 55,439,472-55,439,581	DNAAF4, DNAAF4-CCPG1
nsv3887587	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 55,731,670-55,731,779 , GRCh38 chr15: 55,439,472-55,439,581	DNAAF4, DNAAF4-CCPG1
nsv5674305	insertion	1	nstd102	human	Pathogenic	GRCh38 chr15: 55,434,909-55,434,909 , GRCh37 chr15: 55,727,107-55,727,107	DNAAF4, DNAAF4-CCPG1
nsv4681965	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 55,710,213-55,801,094 , GRCh38.p12 chr15: 55,418,015-55,508,896	DNAAF4, DNAAF4-CCPG1, 2 more genes
nsv4716478	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr15: 55,729,268-55,732,816 , GRCh38 chr15: 55,437,070-55,440,618	DNAAF4, DNAAF4-CCPG1, 1 more genes
nsv3899193	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 55,655,659-55,664,220 , GRCh38.p12 chr15: 55,363,461-55,372,022	DNAAF4-CCPG1, CCPG1, 1 more genes
nsv4729716	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 55,797,842-55,943,656 , GRCh38.p12 chr15: 55,505,644-55,651,458	DNAAF4, PRTG, 1 more genes
nsv3914320	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 53,481,478-53,599,505 , GRCh37.p13 chr15: 55,694,186-55,812,213 , GRCh38.p12 chr15: 55,401,988-55,520,015	DNAAF4, CCPG1, 3 more genes
nsv3909042	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 55,702,481-55,797,835 , GRCh38.p12 chr15: 55,410,283-55,505,637	DNAAF4, LOC100420711, 2 more genes
nsv6637239	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 55,588,733-55,647,861 , GRCh38.p12 chr15: 55,296,535-55,355,663	DNAAF4-CCPG1, CCPG1, 2 more genes
nsv7094725	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 55,611,449-55,647,630 , GRCh38.p12 chr15: 55,319,251-55,355,432	PIGBOS1, DNAAF4-CCPG1, 2 more genes
nsv5380921	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 55,710,213-55,742,585 , GRCh38.p12 chr15: 55,418,015-55,450,387	DNAAF4, PIERCE2, 2 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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