nat14[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
nsv3908902	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 55,993,436-56,001,665 , GRCh38.p12 chr19: 55,482,069-55,490,298	NAT14, ZNF628, 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	NAT14, 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	NAT14, 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	NAT14, 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	NAT14, 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	NAT14, 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	NAT14, 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	NAT14, 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	NAT14, 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	NAT14, 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	NAT14, 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	NAT14, RNU6-980P, 526 more genes
nsv3922599	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 51,141,518-58,539,965 , NCBI36 chr19: 56,336,587-63,743,144 , GRCh37 chr19: 51,644,775-59,051,332	NAT14, LOC100421130, 475 more genes
nsv3913991	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 57,338,938-63,648,700 , GRCh37 chr19: 52,647,126-58,956,888 , GRCh38 chr19: 52,143,873-58,445,521	NAT14, PEG3, 398 more genes
nsv3923613	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 52,612,432-58,581,203 , GRCh37 chr19: 53,115,685-59,092,570 , NCBI36 chr19: 57,807,497-63,784,382	NAT14, ZNF71-SMIM17, 393 more genes
nsv3919766	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 58,150,121-63,784,382 , GRCh37 chr19: 53,458,309-59,092,570 , GRCh38 chr19: 52,955,056-58,581,203	NAT14, MIR520F, 382 more genes
nsv3890688	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 54,196,216-58,759,679 , GRCh38.p12 chr19: 53,692,962-58,248,313	NAT14, MIR517C, 283 more genes
nsv6291483	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr19: 55,247,893-56,503,347 , GRCh38.p12 chr19: 54,911,986-55,991,981	NAT14, IL11, 62 more genes
nsv3914098	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr19: 60,251,694-62,175,638 , GRCh37 chr19: 55,595,687-57,483,826 , GRCh38 chr19: 55,048,514-56,972,458	NAT14, IL11, 99 more genes
nsv3900902	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 55,779,884-56,896,574 , GRCh38.p12 chr19: 55,268,516-56,385,205	NAT14, SLC25A36P1, 61 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 26

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Number of Variants: 20

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Supplemental Content

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Search details

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