dnaaf3[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
nsv3886554	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr19: 55,159,042-55,166,668 , GRCh37 chr19: 55,670,410-55,678,036	DNAAF3, DNAAF3-AS1
nsv7095224	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 55,644,283-55,678,016 , GRCh38.p12 chr19: 55,132,915-55,166,648	DNAAF3, TNNT1, 2 more genes
nsv6310553	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr19: 55,667,549-55,668,957 , GRCh38.p12 chr19: 55,156,181-55,157,589	DNAAF3, TNNI3, 1 more genes
nsv3909319	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 55,665,527-55,692,769 , GRCh38.p12 chr19: 55,154,159-55,181,401	DNAAF3, TNNI3, 3 more genes
nsv7095670	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 55,644,283-55,668,957 , GRCh38.p12 chr19: 55,132,915-55,157,589	DNAAF3, TNNI3, 2 more genes
nsv6310707	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 55,663,202-55,678,016 , GRCh38.p12 chr19: 55,151,834-55,166,648	DNAAF3, TNNI3, 1 more genes
nsv4681942	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 55,663,192-55,669,009 , GRCh38.p12 chr19: 55,151,824-55,157,641	DNAAF3, TNNI3, 1 more genes
nsv3882967	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr19: 55,151,814-55,157,609 , GRCh37.p13 chr19: 55,663,182-55,668,977	DNAAF3, DNAAF3-AS1, 1 more genes
nsv7095225	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 55,663,202-55,668,957 , GRCh38.p12 chr19: 55,151,834-55,157,589	DNAAF3, TNNI3, 1 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	DNAAF3, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	DNAAF3, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	DNAAF3, LENG8, 2408 more genes
nsv3919076	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 48,432,832-59,083,573 , NCBI36 chr19: 53,124,644-63,775,385 , GRCh38 chr19: 47,929,575-58,572,206	DNAAF3, KCNA7, 697 more genes
nsv3911950	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 48,411,797-59,051,332 , NCBI36 chr19: 53,103,609-63,743,144 , GRCh38 chr19: 47,908,540-58,539,965	DNAAF3, LOC107987270, 694 more genes
nsv3924732	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 49,907,832-58,557,889 , GRCh37 chr19: 50,411,089-59,069,256 , NCBI36 chr19: 55,102,901-63,761,068	DNAAF3, RPL39P37, 556 more genes
nsv4729755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886	DNAAF3, SIGLEC5, 574 more genes
nsv3890862	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 50,489,390-59,095,359 , GRCh38.p12 chr19: 49,986,133-58,583,992	DNAAF3, SIGLECL1, 552 more genes
nsv3923909	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 55,347,589-63,784,382 , GRCh37 chr19: 50,655,777-59,092,570 , GRCh38 chr19: 50,152,520-58,581,203	DNAAF3, OSCAR, 535 more genes
nsv3891963	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 50,740,074-59,097,160 , GRCh38.p12 chr19: 50,236,817-58,585,793	DNAAF3, RPS9, 535 more genes
nsv3916611	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 50,694,476-59,047,185 , NCBI36 chr19: 55,386,288-63,738,997 , GRCh38 chr19: 50,191,219-58,535,818	DNAAF3, RNU6-980P, 526 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 36

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Number of Variants: 20

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Supplemental Content

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