alkbh1[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
nsv3898743	copy number variation	1	nstd102	human	Benign	GRCh37 chr14: 78,146,198-78,205,077 , GRCh38.p12 chr14: 77,679,855-77,738,734	ALKBH1, RPL21P10, 3 more genes
nsv4456664	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 77,274,990-89,803,137 , GRCh38.p12 chr14: 76,808,647-89,336,793	ALKBH1, DYNLL1P2, 126 more genes
nsv3923727	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 70,028,816-82,441,728 , GRCh38 chr14: 69,562,099-81,975,384 , NCBI36 chr14: 69,098,569-81,511,481	ALKBH1, CEP128, 240 more genes
nsv3923448	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 73,413,528-77,578,518 , GRCh38 chr14: 73,877,072-78,042,422 , GRCh37 chr14: 74,343,775-78,508,765	ALKBH1, ZC2HC1C, 113 more genes
nsv3922441	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 75,489,052-79,610,332 , GRCh37 chr14: 75,955,395-80,076,675 , NCBI36 chr14: 75,025,148-79,146,428	ALKBH1, IRF2BPL, 69 more genes
nsv3902883	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863	ALKBH1, LOC440181, 1998 more genes
nsv3907460	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456	ALKBH1, BANF1P1, 1996 more genes
nsv3899639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456	ALKBH1, LOC100289511, 1996 more genes
nsv3903256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050	ALKBH1, DHRS7, 1946 more genes
nsv3919106	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482	ALKBH1, SRMP2, 1929 more genes
nsv3904265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229	ALKBH1, CRIP1, 1929 more genes
nsv3917422	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478	ALKBH1, MIR656, 1918 more genes
nsv6315524	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013	ALKBH1, PAPOLA-DT, 1338 more genes
nsv3898512	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 73,750,741-107,285,437 , GRCh38.p12 chr14: 73,284,033-106,877,229	ALKBH1, MEG3, 860 more genes
nsv3922094	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 73,655,772-106,879,298 , GRCh37 chr14: 74,122,475-107,287,505 , NCBI36 chr14: 73,192,228-106,358,550	ALKBH1, LOC105370614, 849 more genes
nsv3915681	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 76,758,891-106,358,550 , GRCh37 chr14: 77,689,138-107,287,505 , GRCh38 chr14: 77,222,795-106,879,298	ALKBH1, IGHV3-32, 751 more genes
nsv3919051	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr14: 72,879,674-78,371,155 , GRCh37 chr14: 73,809,921-79,301,402 , GRCh38 chr14: 73,343,213-78,835,059	ALKBH1, ACYP1, 137 more genes
nsv3911386	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr14: 76,729,101-80,012,228 , GRCh37 chr14: 77,659,348-80,942,475 , GRCh38 chr14: 77,193,005-80,476,132	ALKBH1, DIO2, 38 more genes
nsv3905495	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 76,082,940-78,372,356 , GRCh38.p12 chr14: 75,616,597-77,906,013	ALKBH1, SLIRP, 53 more genes
nsv3904908	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 78,146,198-78,504,237 , GRCh38.p12 chr14: 77,679,855-78,037,894	ALKBH1, SNW1, 7 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 25

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

Recent activity