c11orf65[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
nsv3905052	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 108,256,541-108,267,527 , GRCh38.p12 chr11: 108,385,814-108,396,800	C11ORF65
nsv3907288	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 108,256,859-108,267,527 , GRCh38.p12 chr11: 108,386,132-108,396,800	C11ORF65
nsv5980373	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 108,098,332-108,236,255 , GRCh38.p12 chr11: 108,227,605-108,365,528	C11ORF65, ATM
nsv5672618	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 108,098,346-108,236,241 , GRCh38.p12 chr11: 108,227,619-108,365,514	C11ORF65, ATM
nsv7093908	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 108,099,885-108,225,621 , GRCh38.p12 chr11: 108,229,158-108,354,894	C11ORF65, ATM
nsv3880611	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 108,243,953-108,369,099 , GRCh37 chr11: 108,114,680-108,239,826	C11ORF65, ATM
nsv5672542	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 108,114,660-108,236,235 , GRCh38.p12 chr11: 108,243,933-108,365,508	C11ORF65, ATM
nsv3889791	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 108,243,943-108,365,518 , GRCh37 chr11: 108,114,670-108,236,245	C11ORF65, ATM
nsv7093829	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 108,224,473-108,332,286 , GRCh38.p12 chr11: 108,353,746-108,461,559	C11ORF65, ATM
nsv5672544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 108,124,486-108,225,611 , GRCh38.p12 chr11: 108,253,759-108,354,884	C11ORF65, ATM
nsv4452762	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr11: 108,137,888-108,236,245 , GRCh38 chr11: 108,267,161-108,365,518	C11ORF65, ATM
nsv3880553	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 108,137,892-108,236,241 , GRCh38 chr11: 108,267,165-108,365,514	C11ORF65, ATM
nsv7098740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 108,108,886-108,205,398 , GRCh38.p12 chr11: 108,238,159-108,334,671	C11ORF65, ATM
nsv4452846	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 108,151,712-108,236,245 , GRCh38 chr11: 108,280,985-108,365,518	C11ORF65, ATM
nsv1398511	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 108,280,995-108,365,509 , GRCh37 chr11: 108,151,722-108,236,236	C11ORF65, ATM
nsv7093826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 108,153,427-108,236,235 , GRCh38.p12 chr11: 108,282,700-108,365,508	C11ORF65, ATM
nsv6308955	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 108,164,020-108,236,235 , GRCh38.p12 chr11: 108,293,293-108,365,508	C11ORF65, ATM
nsv3874428	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 108,150,212-108,216,641 , GRCh38.p12 chr11: 108,279,485-108,345,914	C11ORF65, ATM
nsv7093909	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 108,114,660-108,181,062 , GRCh38.p12 chr11: 108,243,933-108,310,335	C11ORF65, ATM
nsv3880037	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 108,178,618-108,236,241 , GRCh38.p12 chr11: 108,307,891-108,365,514	C11ORF65, ATM

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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 144

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Number of Variants: 20

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