pc[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
nsv3882018	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 179,158,880-179,343,766 , GRCh37 chr5: 178,585,881-178,770,767	ADAMTS2
nsv3879923	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 88,928,866-88,996,866 , GRCh38 chr4: 88,007,714-88,075,714	PKD2
nsv3888170	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 88,007,714-88,058,123 , GRCh37 chr4: 88,928,866-88,979,275	PKD2
nsv4683511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 88,959,383-88,996,866 , GRCh38.p12 chr4: 88,038,231-88,075,714	PKD2
nsv3887218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,163,763-2,179,490 , GRCh38 chr16: 2,113,762-2,129,489	PKD1
nsv5381618	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 131,885,763-131,891,377 , GRCh37 chr6: 132,206,903-132,212,517	ENPP1
nsv5673736	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 88,984,922-88,989,952 , GRCh38 chr4: 88,063,770-88,068,800	PKD2
nsv5564221	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 2,099,641-2,103,226 , GRCh37 chr16: 2,149,642-2,153,227	PKD1
nsv3887367	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,152,062-2,152,634 , GRCh38.p12 chr16: 2,102,061-2,102,633	PKD1
nsv7097136	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 178,634,504-178,634,726 , GRCh38.p12 chr5: 179,207,503-179,207,725	ADAMTS2
nsv4682872	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 178,699,902-178,700,075 , GRCh38.p12 chr5: 179,272,901-179,273,074 , GRCh38.p12 chr5\|NW_016107298.1: 37,608-37,781	ADAMTS2
nsv997226	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr4: 88,007,647-88,077,779 , GRCh37 chr4: 88,928,799-88,998,931	PKD2
nsv3879659	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 88,957,372-88,957,372 , GRCh38.p12 chr4: 88,036,220-88,036,220	PKD2
nsv7093067	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 88,940,724-88,959,402 , GRCh38.p12 chr4: 88,019,572-88,038,250	PKD2
nsv6112762	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 88,973,122-88,979,275 , GRCh38.p12 chr4: 88,051,970-88,058,123	PKD2
nsv7096326	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 128,176,278-128,177,573 , GRCh38.p12 chr2: 127,418,702-127,419,997	PROC
nsv6312289	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr5: 178,548,652-178,700,075 , GRCh38.p12 chr5: 179,121,651-179,273,074	ADAMTS2
nsv5673760	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr5: 178,554,950-178,564,955 , GRCh38.p12 chr5: 179,127,949-179,137,954	ADAMTS2
nsv3888663	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr16: 2,154,499-2,154,643 , GRCh38.p12 chr16: 2,104,498-2,104,642	PKD1
nsv3886302	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 88,928,738-88,933,584 , GRCh38.p12 chr4: 88,007,586-88,012,432	PKD2

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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 544

Page of 28

Number of Variants: 20

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