sec23b[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
nsv4684075	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr20: 18,492,869-18,496,380 , GRCh38.p12 chr20: 18,512,225-18,515,736	SEC23B
nsv4450466	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 18,512,225-18,515,736 , GRCh37 chr20: 18,492,869-18,496,380	SEC23B
nsv7095547	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 18,516,277-18,516,406 , GRCh38.p12 chr20: 18,535,633-18,535,762	SEC23B
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	SEC23B, PGAM3P, 182 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	SEC23B, CST3, 146 more genes
nsv3914224	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 17,753,416-21,407,427 , NCBI36 chr20: 17,701,416-21,355,427 , GRCh38 chr20: 17,772,771-21,426,789	SEC23B, LOC107985440, 73 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	SEC23B, 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	SEC23B, 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	SEC23B, 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	SEC23B, 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	SEC23B, 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	SEC23B, 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	SEC23B, 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	SEC23B, 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	SEC23B, 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	SEC23B, 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	SEC23B, 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	SEC23B, 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	SEC23B, 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	SEC23B, KRT18P3, 413 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 32

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Number of Variants: 20

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