cdhr1[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
nsv5672532	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 85,954,517-85,960,443 , GRCh38.p12 chr10: 84,194,761-84,200,687	CDHR1
nsv7093806	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 85,954,517-85,957,612 , GRCh38.p12 chr10: 84,194,761-84,197,856	CDHR1
nsv7093736	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 85,954,517-85,955,365 , GRCh38.p12 chr10: 84,194,761-84,195,609	CDHR1
nsv7093808	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 85,960,337-85,974,377 , GRCh38.p12 chr10: 84,200,581-84,214,621	CDHR1
nsv4682684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 85,955,250-85,982,436 , GRCh38.p12 chr10: 84,195,494-84,222,680	CDHR1, LRIT2
nsv4456535	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 85,956,858-85,982,798 , GRCh38.p12 chr10: 84,197,102-84,223,042	CDHR1, LRIT2
nsv7093807	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 85,954,517-86,018,395 , GRCh38.p12 chr10: 84,194,761-84,258,639	CDHR1, LRIT1, 2 more genes
nsv4683022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 85,901,257-86,018,395 , GRCh38.p12 chr10: 84,141,501-84,258,639	CDHR1, RGR, 5 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	CDHR1, RNU7-12P, 1876 more genes
nsv3920295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422	CDHR1, EIF2S2P3, 895 more genes
nsv6637542	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 82,595,472-93,542,416 , GRCh38.p12 chr10: 80,835,716-91,782,659	CDHR1, IFIT6P, 166 more genes
nsv3891568	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 83,379,241-93,219,169 , GRCh38.p12 chr10: 81,619,485-91,459,412	CDHR1, NAPGP1, 157 more genes
nsv6634458	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 83,533,660-91,913,077 , GRCh38.p12 chr10: 81,773,904-90,153,320	CDHR1, IFIT5, 140 more genes
nsv4729484	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 81,457,752-89,253,430 , GRCh38.p12 chr10: 79,697,996-87,493,673	CDHR1, DPY19L2P5, 115 more genes
nsv3923084	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,149,191-89,108,131 , GRCh38 chr10: 79,719,429-87,358,394 , GRCh37 chr10: 81,479,185-89,118,151	CDHR1, LINC02650, 110 more genes
nsv3910996	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,541,288-89,108,131 , GRCh38 chr10: 79,802,022-87,358,394 , GRCh37 chr10: 81,561,459-89,118,151	CDHR1, HMGN2P8, 110 more genes
nsv3910032	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 81,449,116-88,983,530 , NCBI36 chr10: 81,119,122-88,973,510 , GRCh38 chr10: 79,689,360-87,223,773	CDHR1, LINC02655, 109 more genes
nsv4729317	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 81,617,260-89,146,780 , GRCh38.p12 chr10: 79,857,504-87,387,023	CDHR1, LOC105378390, 109 more genes
nsv4728260	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 81,585,301-89,101,700 , GRCh38.p12 chr10: 79,825,545-87,341,943	CDHR1, C1DP3, 109 more genes
nsv3910650	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,648,252-89,108,131 , GRCh38 chr10: 79,898,516-87,358,394 , GRCh37 chr10: 81,658,272-89,118,151	CDHR1, ZNRF2P3, 103 more genes

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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 54

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Number of Variants: 20

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