post[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
nsv5672847	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 68,820,946-68,842,761 , GRCh38.p12 chr16: 68,787,043-68,808,858	CDH1
nsv4681603	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 68,820,946-68,835,806 , GRCh38.p12 chr16: 68,787,043-68,801,903	CDH1
nsv4768312	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,605,269-130,618,535 , GRCh38.p12 chr9: 127,842,990-127,856,256	ENG
nsv3885668	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 52,306,239-52,314,697 , GRCh38.p12 chr12: 51,912,455-51,920,913	ACVRL1
nsv4450114	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 51,912,465-51,920,903 , GRCh37 chr12: 52,306,249-52,314,687	ACVRL1
nsv3889625	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 51,913,539-51,919,135 , GRCh37 chr12: 52,307,323-52,312,919	ACVRL1
nsv4451527	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 68,862,067-68,867,412 , GRCh38 chr16: 68,828,164-68,833,509	CDH1
nsv4681031	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 68,862,067-68,867,402 , GRCh38.p12 chr16: 68,828,164-68,833,499	CDH1
nsv3880641	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 52,307,738-52,312,919 , GRCh38 chr12: 51,913,954-51,919,135	ACVRL1
nsv4728574	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,605,269-130,609,751 , GRCh38 chr9: 127,842,990-127,847,472	ENG
nsv7094858	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 68,845,577-68,849,672 , GRCh38.p12 chr16: 68,811,674-68,815,769	CDH1
nsv5673003	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 68,863,547-68,867,402 , GRCh38.p12 chr16: 68,829,644-68,833,499	CDH1
nsv6309322	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 52,306,863-52,310,037 , GRCh38.p12 chr12: 51,913,079-51,916,253	ACVRL1
nsv4681732	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 52,306,873-52,310,027 , GRCh38.p12 chr12: 51,913,089-51,916,243	ACVRL1
nsv3887785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 52,314,543-52,317,145 , GRCh38 chr12: 51,920,759-51,923,361	ACVRL1
nsv4681766	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 68,862,067-68,863,710 , GRCh38.p12 chr16: 68,828,164-68,829,807	CDH1
nsv3873803	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 68,862,071-68,863,706 , GRCh38 chr16: 68,828,168-68,829,803	CDH1
nsv6309321	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 52,306,259-52,307,877 , GRCh38.p12 chr12: 51,912,475-51,914,093	ACVRL1
nsv7094688	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 68,861,950-68,863,561 , GRCh38.p12 chr16: 68,828,047-68,829,658	CDH1
nsv3880354	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr16: 68,737,292-68,738,411 , GRCh37.p13 chr16: 68,771,195-68,772,314	CDH1

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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 170

Page of 9

Number of Variants: 20

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Supplemental Content

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