apmap[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
nsv4730008	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 24,685,850-24,948,039 , GRCh38.p12 chr20: 24,705,214-24,967,403	APMAP, LINC02967, 2 more genes
nsv3891787	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 18,500,917-25,847,320 , GRCh38.p12 chr20: 18,520,273-25,866,684	APMAP, CST3, 146 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	APMAP, 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	APMAP, 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	APMAP, 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	APMAP, 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	APMAP, 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	APMAP, 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	APMAP, 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	APMAP, ISM1-AS1, 498 more genes
nsv3910142	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 9,792,081-37,945,599 , GRCh38 chr20: 9,811,433-39,316,956 , NCBI36 chr20: 9,740,081-37,379,013	APMAP, DYNLRB1, 555 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	APMAP, 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	APMAP, 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	APMAP, 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	APMAP, NRSN2, 459 more genes
nsv3904899	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 17,705,775-31,600,738 , GRCh38.p12 chr20: 17,725,130-33,012,932	APMAP, TTLL9, 297 more genes
nsv3878906	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 17,705,775-31,600,738 , GRCh38.p12 chr20: 17,725,130-33,012,932	APMAP, KIF3B, 297 more genes
nsv3913354	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 22,061,586-30,285,812 , GRCh37 chr20: 22,042,224-29,520,488 , NCBI36 chr20: 21,990,224-28,134,149	APMAP, LOC391239, 127 more genes
nsv6291578	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413	APMAP, AHCY, 330 more genes
nsv4729757	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 19,750,804-30,479,077 , GRCh38.p12 chr20: 19,770,160-31,891,274	APMAP, BCL2L1, 222 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 25

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Number of Variants: 20

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Supplemental Content

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