cpxm1[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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	CPXM1, LOC101929098, 121 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	CPXM1, 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	CPXM1, 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	CPXM1, 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	CPXM1, 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	CPXM1, 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	CPXM1, 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	CPXM1, 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	CPXM1, 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	CPXM1, 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	CPXM1, 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	CPXM1, 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	CPXM1, 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	CPXM1, 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	CPXM1, PTMAP3, 331 more genes
nsv3914413	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-19,000,139 , GRCh38 chr20: 89,939-19,071,495 , GRCh37 chr20: 70,580-19,052,139	CPXM1, ZNF343, 331 more genes
nsv3914070	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 80,928-18,688,031 , NCBI36 chr20: 9,569-18,616,675 , GRCh37 chr20: 61,569-18,668,675	CPXM1, CDC25B, 324 more genes
nsv3923490	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 80,106-13,029,401 , NCBI36 chr20: 8,747-12,958,049 , GRCh37 chr20: 60,747-13,010,049	CPXM1, LINC01751, 238 more genes
nsv3913573	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 1,269,303-8,626,911 , NCBI36 chr20: 1,197,947-8,555,558 , GRCh37 chr20: 1,249,947-8,607,558	CPXM1, LINC01433, 158 more genes
nsv3912889	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 8,734-6,314,659 , GRCh37 chr20: 60,734-6,366,659 , GRCh38 chr20: 80,093-6,386,012	CPXM1, IDH3B, 172 more genes

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

Send to:

Search results

Items: 1 to 20 of 31

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

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 31

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity