pcna[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
nsv7095797	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 5,081,437-5,093,674 , GRCh38.p12 chr20: 5,100,791-5,113,028	PCNA, TMEM230
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	PCNA, LOC107985398, 178 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	PCNA, 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	PCNA, PGAM3P, 102 more genes
nsv3906854	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 2,463,101-8,185,680 , GRCh38.p12 chr20: 2,482,455-8,205,033	PCNA, LOC101929098, 121 more genes
nsv3913207	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 4,343,033-6,911,730 , GRCh37 chr20: 4,323,680-6,892,377 , NCBI36 chr20: 4,271,680-6,840,377	PCNA, RNA5-8SP7, 45 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	PCNA, 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	PCNA, 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	PCNA, 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	PCNA, 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	PCNA, 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	PCNA, 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	PCNA, 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	PCNA, ISM1-AS1, 498 more genes
nsv4349190	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843	PCNA, LOC105372582, 473 more genes
nsv3919898	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,568-26,305,479 , GRCh38 chr20: 80,927-26,324,843 , NCBI36 chr20: 9,568-26,253,479	PCNA, MIR3192, 473 more genes
nsv3907558	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 80,198-26,075,841 , GRCh38.p12 chr20: 99,557-26,095,205	PCNA, LINC03086, 469 more genes
nsv3913704	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 89,939-25,697,564 , NCBI36 chr20: 18,580-25,626,200 , GRCh37 chr20: 70,580-25,678,200	PCNA, NRSN2, 459 more genes
nsv7148267	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102	PCNA, KRT18P3, 413 more genes
nsv3921972	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-19,074,923 , GRCh38 chr20: 89,939-19,146,279 , GRCh37 chr20: 70,580-19,126,923	PCNA, PTMAP3, 331 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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