mkks[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
nsv3883445	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 10,405,227-10,413,534 , GRCh37 chr20: 10,385,875-10,394,182	MKKS
nsv5059991	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 10,412,470-10,413,555 , GRCh37 chr20: 10,393,118-10,394,203	MKKS
nsv3905532	copy number variation	1	nstd102	human	Benign	GRCh37 chr20: 10,384,819-10,650,354 , GRCh38.p12 chr20: 10,404,171-10,669,706	MKKS, MIR6870, 3 more genes
nsv4449772	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 10,234,257-10,654,198 , GRCh38 chr20: 10,253,609-10,673,550	MKKS, JAG1, 7 more genes
nsv3890981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 3,092,739-17,091,453 , GRCh38.p12 chr20: 3,112,093-17,110,808	MKKS, LOC107985398, 178 more genes
nsv4676419	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 8,571,696-22,088,650 , GRCh38.p12 chr20: 8,591,049-22,108,012	MKKS, PGAM3P, 182 more genes
nsv6315526	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 3,178,539-11,848,383 , GRCh38.p12 chr20: 3,197,893-11,867,735	MKKS, LRRN4, 129 more genes
nsv3897192	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 4,392,930-12,667,768 , GRCh38.p12 chr20: 4,412,283-12,687,121	MKKS, PGAM3P, 102 more genes
nsv3920089	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 6,617,695-13,392,559 , NCBI36 chr20: 6,546,342-13,321,206 , GRCh37 chr20: 6,598,342-13,373,206	MKKS, RN7SKP111, 68 more genes
nsv3911315	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 7,547,291-11,009,342 , NCBI36 chr20: 7,495,291-10,957,342 , GRCh38 chr20: 7,566,644-11,028,694	MKKS, RNU105B, 34 more genes
nsv3922170	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 9,479,622-12,012,082 , GRCh38 chr20: 9,550,975-12,083,434 , GRCh37 chr20: 9,531,622-12,064,082	MKKS, LOC107985384, 32 more genes
nsv4349454	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 10,124,855-11,479,105 , GRCh38.p12 chr20: 10,144,207-11,498,457	MKKS, SNAP25, 19 more genes
nsv3892750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941	MKKS, TGIF2-RAB5IF, 1314 more genes
nsv3905072	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435	MKKS, LRRN4, 1313 more genes
nsv3895314	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202	MKKS, PKIG, 1311 more genes
nsv3896520	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110	MKKS, COMMD7, 1311 more genes
nsv3920218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118	MKKS, MIR3646, 1310 more genes
nsv3908959	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 67,837-29,638,363 , GRCh38.p12 chr20: 87,196-30,403,687	MKKS, ISM1-AS1, 504 more genes
nsv3913796	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-28,133,653 , GRCh37.p13 chr20: 70,580-29,519,992 , GRCh38.p12 chr20: 89,939-30,285,316	MKKS, RNY4P11, 500 more genes
nsv3922272	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 80,106-30,227,427 , NCBI36 chr20: 8,747-28,075,764 , GRCh37 chr20: 60,747-29,462,103	MKKS, ISM1-AS1, 498 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 36

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Number of Variants: 20

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Supplemental Content

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