cpne9[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
nsv3905232	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 32,241-12,681,483 , GRCh37 chr3: 73,914-12,722,982 , NCBI36 chr3: 48,914-12,697,982	CPNE9, OR7E122P, 163 more genes
nsv3885461	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-12,575,409 , GRCh38.p12 chr3: 20,213-12,533,910	CPNE9, MARK2P14, 160 more genes
nsv6636276	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-11,679,509 , GRCh38.p12 chr3: 20,214-11,638,035	CPNE9, RPL23AP39, 144 more genes
nsv3906827	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 32,241-11,379,835 , GRCh37 chr3: 73,914-11,421,309 , NCBI36 chr3: 48,914-11,396,309	CPNE9, LOC107986040, 142 more genes
nsv3895550	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 20,213-11,221,602 , NCBI36 chr3: 36,891-11,238,288 , GRCh37 chr3: 61,891-11,263,288	CPNE9, SRGAP3, 141 more genes
nsv3900952	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 52,266-11,089,569 , NCBI36 chr3: 68,949-11,106,255 , GRCh37 chr3: 93,949-11,131,255	CPNE9, RPUSD3, 137 more genes
nsv3900980	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 73,914-10,672,995 , GRCh38 chr3: 32,241-10,631,310 , NCBI36 chr3: 48,914-10,647,995	CPNE9, MIR885, 131 more genes
nsv3892568	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 705,581-11,067,828 , GRCh37 chr3: 730,581-11,092,828 , GRCh38 chr3: 688,897-11,051,142	CPNE9, DUSP5P2, 126 more genes
nsv3894686	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 48,914-10,339,808 , GRCh38 chr3: 32,241-10,323,124 , GRCh37 chr3: 73,914-10,364,808	CPNE9, RPL21P17, 128 more genes
nsv4674715	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-10,287,825 , GRCh38.p12 chr3: 20,213-10,246,141	CPNE9, LOC105376944, 122 more genes
nsv3889023	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-10,104,842 , GRCh38.p12 chr3: 20,213-10,063,158	CPNE9, TTLL3, 118 more genes
nsv6636296	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-9,899,605 , GRCh38.p12 chr3: 20,214-9,857,921	CPNE9, GRM7-AS1, 101 more genes
nsv6313525	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-9,797,094 , GRCh38.p12 chr3: 20,213-9,755,410	CPNE9, EGOT, 95 more genes
nsv6636323	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-9,769,457 , GRCh38.p12 chr3: 20,214-9,727,773	CPNE9, LOC107984112, 92 more genes
nsv7148084	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 3,669,542-9,937,745 , GRCh38.p12 chr3: 3,627,858-9,896,061	CPNE9, LOC105376943, 71 more genes
nsv3880780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 8,922,160-12,338,637 , GRCh38.p12 chr3: 8,880,476-12,297,138	CPNE9, IL17RC, 77 more genes
nsv3882563	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 6,842,555-10,153,209 , GRCh38.p12 chr3: 6,800,868-10,111,525	CPNE9, LOC107984112, 57 more genes
nsv3911723	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 9,436,558-11,732,086 , GRCh38 chr3: 9,394,874-11,690,612 , NCBI36 chr3: 9,411,558-11,707,086	CPNE9, FANCD2, 57 more genes
nsv3924927	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 9,695,981-10,270,371 , NCBI36 chr3: 9,670,981-10,245,371 , GRCh38 chr3: 9,654,297-10,228,687	CPNE9, CIDECP1, 30 more genes
nsv3910678	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 9,410,033-9,972,855 , GRCh37 chr3: 9,435,033-9,997,855 , GRCh38 chr3: 9,393,349-9,956,171	CPNE9, LHFPL4, 22 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 57

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Number of Variants: 20

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