rtel1[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
nsv5673182	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 62,290,746-62,312,082 , GRCh38.p12 chr20: 63,659,393-63,680,729	RTEL1, RTEL1-TNFRSF6B
nsv6311096	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 62,298,812-62,303,984 , GRCh38.p12 chr20: 63,667,459-63,672,631	RTEL1, RTEL1-TNFRSF6B
nsv5673330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 62,290,746-62,290,867 , GRCh38.p12 chr20: 63,659,393-63,659,514	RTEL1, RTEL1-TNFRSF6B
nsv5673331	copy number variation	2	nstd102	human	Pathogenic, Likely pathogenic	GRCh37 chr20: 62,298,812-62,298,916 , GRCh38.p12 chr20: 63,667,459-63,667,563	RTEL1, RTEL1-TNFRSF6B
nsv6137848	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 62,323,095-62,324,636 , GRCh38.p12 chr20: 63,691,742-63,693,283	RTEL1, RTEL1-TNFRSF6B
nsv7093127	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 62,325,127-62,325,799 , GRCh38 chr20: 63,693,774-63,694,446	RTEL1, RTEL1-TNFRSF6B
nsv6311075	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 62,316,900-62,316,977 , GRCh38 chr20: 63,685,547-63,685,624	RTEL1, RTEL1-TNFRSF6B
nsv5673258	copy number variation	2	nstd102	human	Likely pathogenic	GRCh37 chr20: 62,316,913-62,316,990 , GRCh38 chr20: 63,685,560-63,685,637	RTEL1, RTEL1-TNFRSF6B
nsv6311059	copy number variation	2	nstd102	human	Pathogenic, Likely pathogenic	GRCh37 chr20: 62,309,488-62,312,082 , GRCh38.p12 chr20: 63,678,135-63,680,729	RTEL1, RTEL1-TNFRSF6B
nsv5673415	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr20: 63,685,601-63,685,678 , GRCh37 chr20: 62,316,954-62,317,031	RTEL1, RTEL1-TNFRSF6B
nsv4681602	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 62,290,756-62,324,646 , GRCh38.p12 chr20: 63,659,403-63,693,293	RTEL1, RTEL1-TNFRSF6B
nsv6290223	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 62,316,953-62,316,954 , GRCh38 chr20: 63,685,600-63,685,601	RTEL1, RTEL1-TNFRSF6B
nsv7096085	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 62,309,478-62,329,916 , GRCh38.p12 chr20: 63,678,125-63,698,563	RTEL1, TNFRSF6B, 2 more genes
nsv7096272	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 62,316,856-62,327,211 , GRCh38.p12 chr20: 63,685,503-63,695,858	RTEL1, TNFRSF6B, 1 more genes
nsv5673183	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 62,292,641-62,327,221 , GRCh38.p12 chr20: 63,661,288-63,695,868	RTEL1, TNFRSF6B, 1 more genes
nsv3901897	copy number variation	1	nstd102	human	Benign	GRCh37 chr20: 62,326,104-62,336,258 , GRCh38.p12 chr20: 63,694,751-63,704,906	RTEL1, ARFRP1, 2 more genes
nsv3905040	copy number variation	1	nstd102	human	Benign	GRCh37 chr20: 62,326,104-62,332,436 , GRCh38.p12 chr20: 63,694,751-63,701,084	RTEL1, ARFRP1, 2 more genes
nsv3905736	copy number variation	1	nstd102	human	Benign	GRCh37 chr20: 62,326,104-62,330,484 , GRCh38.p12 chr20: 63,694,751-63,699,131	RTEL1, TNFRSF6B, 2 more genes
nsv7096086	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 62,325,715-62,326,337 , GRCh38.p12 chr20: 63,694,362-63,694,984	RTEL1, TNFRSF6B, 1 more genes
nsv6310916	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 62,290,756-62,328,484 , GRCh38.p12 chr20: 63,659,403-63,697,131	RTEL1, ARFRP1, 2 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 92

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Number of Variants: 20

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