klf15[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
nsv3872106	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 126,068,557-126,076,461 , GRCh38.p12 chr3: 126,349,714-126,357,618	KLF15
nsv3873138	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 126,068,779-126,076,461 , GRCh38.p12 chr3: 126,349,936-126,357,618	KLF15
nsv3918094	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 113,822,514-129,935,667 , GRCh38 chr3: 112,620,977-128,734,134 , GRCh37 chr3: 112,339,824-128,452,977	KLF15, QTRT2, 284 more genes
nsv6311770	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 120,365,818-133,465,047 , GRCh38.p12 chr3: 120,646,971-133,746,203	KLF15, HNRNPA1P23, 278 more genes
nsv6112688	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144	KLF15, RNU4-62P, 169 more genes
nsv3924082	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 119,875,435-127,742,263 , GRCh38 chr3: 118,673,898-126,540,730 , GRCh37 chr3: 118,392,745-126,259,573	KLF15, MYLK-AS2, 165 more genes
nsv6112709	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 123,000,000-129,700,000 , GRCh38.p12 chr3: 123,281,153-129,981,157	KLF15, OR7E97P, 160 more genes
nsv3913250	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 123,126,684-127,983,782 , GRCh38 chr3: 121,925,147-126,782,249 , GRCh37 chr3: 121,643,994-126,501,092	KLF15, RPS24P9, 106 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	KLF15, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	KLF15, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	KLF15, RPL23AP49, 2875 more genes
nsv3918981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446	KLF15, LINC02614, 1469 more genes
nsv6637156	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502	KLF15, H1-10, 846 more genes
nsv3922717	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168	KLF15, OR7E53P, 794 more genes
nsv4347357	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 124,369,671-126,423,192 , GRCh38.p12 chr3: 124,650,824-126,704,349	KLF15, ITGB5, 63 more genes
nsv4673909	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 125,826,729-126,040,939 , GRCh38.p12 chr3: 126,107,886-126,322,096	KLF15, LOC105374083, 6 more genes
nsv3920834	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 127,308,312-142,119,621 , GRCh38 chr3: 126,106,779-140,918,089 , GRCh37 chr3: 125,825,622-140,636,931	KLF15, NCK1-DT, 271 more genes
nsv6313832	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 124,990,058-126,401,548 , GRCh38.p12 chr3: 125,271,214-126,682,705	KLF15, LOC100419966, 50 more genes
nsv6315343	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 124,981,934-126,093,700 , GRCh38.p12 chr3: 125,263,090-126,374,857	KLF15, LOC107986124, 38 more genes
nsv4454406	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 124,981,934-126,088,215 , GRCh38.p12 chr3: 125,263,090-126,369,372	KLF15, LOC105374080, 37 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

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Search details

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