cdk13[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
nsv3873279	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr7: 39,960,093-40,104,664 , GRCh37 chr7: 39,999,692-40,144,263	CDK13
nsv3920693	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr7: 39,974,976-40,061,635 , GRCh37 chr7: 40,008,451-40,095,110 , GRCh38 chr7: 39,968,852-40,055,511	CDK13
nsv6290899	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 40,025,231-40,097,935 , GRCh38.p12 chr7: 39,985,632-40,058,336	CDK13
nsv7097625	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 40,027,178-40,134,579 , GRCh38.p12 chr7: 39,987,579-40,094,980	CDK13
nsv7098120	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 39,990,241-40,041,650 , GRCh38.p12 chr7: 39,950,642-40,002,051	CDK13
nsv7097741	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 40,102,405-40,134,579 , GRCh38.p12 chr7: 40,062,806-40,094,980	CDK13
nsv7097370	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 39,990,241-39,991,471 , GRCh38.p12 chr7: 39,950,642-39,951,872	CDK13
nsv6313651	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 40,116,335-40,240,160 , GRCh38.p12 chr7: 40,076,736-40,200,561	CDK13, HIGD1AP7, 3 more genes
nsv3894552	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr7: 40,095,110-40,256,612 , GRCh38.p12 chr7: 40,055,511-40,217,013	CDK13, MPLKIP, 3 more genes
nsv6291051	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 40,102,960-40,207,962 , GRCh38.p12 chr7: 40,063,361-40,168,363	CDK13, SUGCT, 3 more genes
nsv6291235	copy number variation	1	nstd102	human	not provided	GRCh37 chr7: 40,026,937-40,170,245 , GRCh38.p12 chr7: 39,987,338-40,130,646	CDK13, MPLKIP, 1 more genes
nsv7097371	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 40,085,415-40,174,739 , GRCh38.p12 chr7: 40,045,816-40,135,140	CDK13, SUGCT, 2 more genes
nsv6312543	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 40,127,705-40,174,739 , GRCh38.p12 chr7: 40,088,106-40,135,140	CDK13, SUGCT, 2 more genes
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	CDK13, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	CDK13, LOC107986817, 2014 more genes
nsv3897424	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 32,911,003-44,576,005 , GRCh38.p12 chr7: 32,871,391-44,536,406	CDK13, LOC107986734, 192 more genes
nsv3916442	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 37,309,607-48,670,880 , GRCh37 chr7: 37,343,082-48,700,334 , GRCh38 chr7: 37,303,478-48,660,738	CDK13, LOC102724903, 204 more genes
nsv3911166	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 40,060,197-50,611,198 , NCBI36 chr7: 40,026,722-50,578,692 , GRCh38 chr7: 40,020,598-50,543,500	CDK13, SUGCT, 155 more genes
nsv3912277	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 32,684,528-41,051,106 , GRCh37 chr7: 32,718,003-41,084,581 , GRCh38 chr7: 32,678,391-41,044,983	CDK13, MATCAP2, 134 more genes
nsv3924742	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 38,217,601-45,343,699 , GRCh38 chr7: 38,177,999-45,304,100 , NCBI36 chr7: 38,184,126-45,310,224	CDK13, NUDCD3, 152 more genes

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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 45

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Number of Variants: 20

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