cdh2[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
nsv7094929	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 25,532,117-25,756,986 , GRCh38.p12 chr18: 27,952,153-28,177,022	CDH2
nsv7095435	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 25,727,617-25,756,986 , GRCh38.p12 chr18: 28,147,653-28,177,022	CDH2
nsv6634532	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 25,530,926-25,543,320 , GRCh38.p12 chr18: 27,950,962-27,963,356	CDH2
nsv7095434	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 25,532,117-25,543,505 , GRCh38.p12 chr18: 27,952,153-27,963,541	CDH2
nsv7095375	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 25,532,117-25,532,343 , GRCh38.p12 chr18: 27,952,153-27,952,379	CDH2
nsv3895445	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr18: 25,329,706-25,994,263 , GRCh38.p12 chr18: 27,749,742-28,414,299	CDH2, LOC105372042
nsv6314722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520	CDH2, LOC107985176, 632 more genes
nsv3900710	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 20,069,932-36,887,326 , GRCh38.p12 chr18: 22,489,969-39,307,362	CDH2, CABLES1, 174 more genes
nsv4676233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 22,868,759-34,335,753 , GRCh38.p12 chr18: 25,288,795-36,755,790	CDH2, DHFRP1, 116 more genes
nsv4729854	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 23,971,647-33,737,300 , GRCh38.p12 chr18: 26,391,683-36,157,337	CDH2, CLUHP6, 100 more genes
nsv6315530	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271	CDH2, LOC105372145, 947 more genes
nsv3907444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 12,842-78,015,180 , GRCh38.p12 chr18: 12,842-80,257,297	CDH2, GALNT1, 947 more genes
nsv3890669	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 13,034-78,015,180 , GRCh38.p12 chr18: 13,034-80,257,297	CDH2, MYL12B, 947 more genes
nsv3918488	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 43,345-76,068,860 , GRCh38 chr18: 53,345-80,209,986 , GRCh37 chr18: 53,345-77,967,869	CDH2, LOC105372027, 945 more genes
nsv3924351	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 108,760-76,113,817 , GRCh38 chr18: 118,760-80,254,946 , GRCh37 chr18: 118,760-78,012,829	CDH2, MIX23P1, 942 more genes
nsv3919004	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 136,226-80,256,240 , GRCh37 chr18: 136,226-78,014,123 , NCBI36 chr18: 126,226-76,115,097	CDH2, LIVAR, 941 more genes
nsv3899451	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,226-78,014,123 , GRCh38.p12 chr18: 136,226-80,256,240	CDH2, BOLA2P1, 941 more genes
nsv3924706	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097	CDH2, LOC100420948, 941 more genes
nsv3907722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,227-78,014,123 , GRCh38.p12 chr18: 136,227-80,256,240	CDH2, ROCK1, 941 more genes
nsv3910887	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 139,089-76,113,807 , GRCh37 chr18: 149,089-78,012,819 , GRCh38 chr18: 149,089-80,254,936	CDH2, LPIN2, 941 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 43

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Number of Variants: 20

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