slfn13[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
nsv7137216	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 30,572,862-35,843,988 , GRCh38.p12 chr17: 32,245,843-36,446,544	SLFN13, PSMD11, 117 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	SLFN13, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	SLFN13, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	SLFN13, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	SLFN13, SMURF2, 2366 more genes
nsv3914783	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577	SLFN13, LOC105371922, 1855 more genes
nsv4457831	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395	SLFN13, LOC105371753, 474 more genes
nsv3908251	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 33,680,811-33,768,199 , GRCh38.p12 chr17: 35,353,792-35,441,180	SLFN13, SLFN12, 4 more genes
nsv3894181	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 33,684,035-33,768,334 , GRCh38.p12 chr17: 35,357,016-35,441,315	SLFN13, SLFN12, 4 more genes
nsv3895001	copy number variation	1	nstd102	human	Benign/Likely benign	GRCh37 chr17: 33,687,356-33,767,930 , GRCh38.p12 chr17: 35,360,337-35,440,911	SLFN13, SLFN12, 4 more genes
nsv3896708	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 33,690,466-33,768,354 , GRCh38.p12 chr17: 35,363,447-35,441,335	SLFN13, SLFN12, 4 more genes
nsv3897770	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr17: 33,498,726-33,863,479 , GRCh38.p12 chr17: 35,171,707-35,536,460	SLFN13, SLFN12L, 15 more genes
nsv3898034	copy number variation	2	nstd102	human	Benign	GRCh37 chr17: 33,684,035-33,768,199 , GRCh38.p12 chr17: 35,357,016-35,441,180	SLFN13, LOC105371933, 4 more genes
nsv3908528	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 33,691,903-33,768,199 , GRCh38.p12 chr17: 35,364,884-35,441,180	SLFN13, SLFN12, 4 more genes
nsv3876148	copy number variation	3	nstd102	human	not provided	GRCh37 chr17: 33,684,035-33,768,199 , GRCh38 chr17: 35,357,016-35,441,180	SLFN13, LOC729839, 4 more genes
nsv3907376	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 32,351,496-34,455,576 , GRCh38.p12 chr17: 34,024,477-35,919,248	SLFN13, CCL8, 67 more genes
nsv4675860	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 33,073,917-33,863,479 , GRCh38.p12 chr17: 34,746,898-35,536,460	SLFN13, RPL37P22, 26 more genes
nsv3914031	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr17: 30,480,991-31,118,181 , GRCh38 chr17: 35,129,859-35,767,049 , GRCh37 chr17: 33,456,878-34,094,068	SLFN13, UFM1P2, 30 more genes
nsv7095147	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 33,475,283-34,079,869 , GRCh38.p12 chr17: 35,148,264-35,752,850	SLFN13, SLC35G3, 26 more genes
nsv6634448	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 33,756,756-34,005,513 , GRCh38.p12 chr17: 35,429,737-35,678,494	SLFN13, LOC100420062, 13 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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