pxmp2[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
nsv6309306	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 133,202,693-133,263,901 , GRCh38.p12 chr12: 132,626,107-132,687,315	PXMP2, POLE
nsv6309257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 133,214,430-133,264,149 , GRCh38.p12 chr12: 132,637,844-132,687,563	PXMP2, POLE
nsv5380897	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 133,225,505-133,263,901 , GRCh38.p12 chr12: 132,648,919-132,687,315	PXMP2, POLE
nsv4682985	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 133,240,580-133,263,911 , GRCh38.p12 chr12: 132,663,994-132,687,325	PXMP2, POLE
nsv6309473	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 133,252,670-133,263,901 , GRCh38.p12 chr12: 132,676,084-132,687,315	PXMP2, POLE
nsv4681657	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr12: 133,263,830-133,263,901 , GRCh38.p12 chr12: 132,687,244-132,687,315	PXMP2, POLE
nsv4682701	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr12: 133,201,283-133,263,901 , GRCh38.p12 chr12: 132,624,697-132,687,315	PXMP2, POLE
nsv4682674	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr12: 133,210,762-133,263,901 , GRCh38.p12 chr12: 132,634,176-132,687,315	PXMP2, POLE
nsv4683068	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr12: 133,233,712-133,263,901 , GRCh38.p12 chr12: 132,657,126-132,687,315	PXMP2, POLE
nsv4452893	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 133,233,712-133,263,911 , GRCh38 chr12: 132,657,126-132,687,325	PXMP2, POLE
nsv3878065	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 133,263,834-133,263,907 , GRCh38.p12 chr12: 132,687,248-132,687,321	PXMP2, POLE
nsv4683426	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 133,201,263-133,263,921 , GRCh38.p12 chr12: 132,624,677-132,687,335	PXMP2, POLE
nsv3885076	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 133,201,273-133,263,911 , GRCh38 chr12: 132,624,687-132,687,325	PXMP2, POLE
nsv3882953	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr12: 132,624,691-132,687,321 , GRCh37 chr12: 133,201,277-133,263,907	PXMP2, POLE
nsv4683045	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 133,208,881-133,263,921 , GRCh38.p12 chr12: 132,632,295-132,687,335	PXMP2, POLE
nsv4682082	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 133,208,891-133,263,901 , GRCh38.p12 chr12: 132,632,305-132,687,315	PXMP2, POLE
nsv4681049	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 133,212,468-133,263,901 , GRCh38.p12 chr12: 132,635,882-132,687,315	PXMP2, POLE
nsv4682876	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 133,214,590-133,263,901 , GRCh38.p12 chr12: 132,638,004-132,687,315	PXMP2, POLE
nsv3876942	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr12: 132,657,136-132,687,359 , GRCh37 chr12: 133,233,722-133,263,945	PXMP2, POLE
nsv4683358	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 133,233,712-133,263,911 , GRCh38.p12 chr12: 132,657,126-132,687,325	PXMP2, POLE

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Number of Variants: 20

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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 66

Page of 4

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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