agxt2[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
nsv3874409	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 34,945,903-35,060,803 , GRCh38.p12 chr5: 34,945,798-35,060,701	AGXT2, DNAJC21, 1 more genes
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	AGXT2, MEGF10, 2080 more genes
nsv3914649	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 22,149-35,831,538 , GRCh37 chr5: 22,149-35,831,640 , NCBI36 chr5: 75,149-35,867,397	AGXT2, LOC105374666, 399 more genes
nsv3914100	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 30,184,899-35,249,537 , GRCh38 chr5: 30,149,035-35,213,678 , GRCh37 chr5: 30,149,142-35,213,780	AGXT2, GUSBP18, 61 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	AGXT2, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	AGXT2, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	AGXT2, SPEF2, 2490 more genes
nsv3911585	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550	AGXT2, LINC02241, 878 more genes
nsv3923992	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 50,093-46,115,086 , NCBI36 chr5: 103,093-46,150,843 , GRCh38 chr5: 49,978-46,114,984	AGXT2, LOC100130748, 533 more genes
nsv3911295	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 54,954-45,649,963 , NCBI36 chr5: 107,954-45,685,720 , GRCh38 chr5: 54,839-45,649,861	AGXT2, PMCHL1, 532 more genes
nsv3922539	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 107,954-35,716,704 , GRCh37 chr5: 54,954-35,680,947 , GRCh38 chr5: 54,839-35,680,845	AGXT2, MTCYBP37, 398 more genes
nsv3889403	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-35,739,404 , GRCh38.p12 chr5: 113,461-35,739,302	AGXT2, LOC101929003, 397 more genes
nsv3882526	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,461,664-46,098,927 , GRCh38.p12 chr5: 13,461,554-46,098,825	AGXT2, TPT1P5, 351 more genes
nsv3918728	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 4,849,498-36,818,719 , NCBI36 chr5: 4,902,611-36,854,578 , GRCh37 chr5: 4,849,611-36,818,821	AGXT2, LINC02100, 334 more genes
nsv6313864	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 26,382,110-46,389,339 , GRCh38.p12 chr5: 26,382,001-46,389,237	AGXT2, LOC107986346, 227 more genes
nsv3875357	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 27,227,243-45,685,844 , GRCh38.p12 chr5: 27,227,136-45,685,742	AGXT2, MRPS30, 224 more genes
nsv6636973	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237	AGXT2, SUB1, 210 more genes
nsv5381781	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929	AGXT2, ST3GAL5P1, 213 more genes
nsv3873925	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 31,351,588-43,480,111 , GRCh38.p12 chr5: 31,351,481-43,480,009	AGXT2, CCDC152, 176 more genes
nsv4456866	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 34,453,883-46,389,339 , GRCh38.p12 chr5: 34,453,778-46,389,237	AGXT2, LOC100506639, 146 more genes

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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 28

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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