cdh16[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
nsv6289846	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 95,186,036-95,301,703 , GRCh38.p12 chr8: 94,173,808-94,289,475	RPL6P23, LOC105375648, 2 more genes
nsv3911034	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 79,584,698-96,379,096 , NCBI36 chr8: 79,747,253-96,448,272 , GRCh38 chr8: 78,672,463-95,366,868	LOC105375933, LOC105375930, 233 more genes
nsv7137123	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 89,179,899-97,978,274 , GRCh38.p12 chr8: 88,167,670-96,966,046	SLC26A7, LOC105375639, 112 more genes
nsv3916762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 62,213,235-67,804,317 , GRCh38 chr16: 62,179,331-67,770,414 , NCBI36 chr16: 60,770,736-66,361,818	CDH16, RANBP10, 87 more genes
nsv3921868	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 93,836,936-98,873,536 , GRCh38 chr8: 92,755,532-97,792,132 , GRCh37 chr8: 93,767,760-98,804,360	MIR8084, GEM, 75 more genes
nsv4675201	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 65,669,673-70,180,183 , GRCh38.p12 chr16: 65,635,770-70,146,280	CDH16, LOC100420066, 143 more genes
nsv3910745	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 62,902,680-66,653,415 , GRCh38 chr16: 64,311,275-68,062,011 , GRCh37 chr16: 64,345,179-68,095,914	CDH16, PSMB10, 95 more genes
nsv3912913	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 92,022,400-95,619,747 , GRCh37 chr8: 91,953,224-95,550,571 , GRCh38 chr8: 90,940,996-94,538,343	LOC101926956, RPL6P23, 51 more genes
nsv3912063	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 93,364,583-96,867,847 , GRCh37 chr8: 93,295,407-96,798,671 , GRCh38 chr8: 92,283,179-95,786,443	LOC102724710, LOC105375647, 56 more genes
nsv3915225	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 92,287,062-95,786,443 , GRCh37 chr8: 93,299,290-96,798,671 , NCBI36 chr8: 93,368,466-96,867,847	LINC02906, LOC105375638, 56 more genes
nsv3920272	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 94,119,579-96,749,186 , GRCh37 chr8: 94,050,403-96,680,010 , GRCh38 chr8: 93,038,175-95,667,782	PLEKHF2, INTS8, 48 more genes
nsv7094682	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 65,821,800-67,208,957 , GRCh38.p12 chr16: 65,787,897-67,175,054	CDH16, RNA5SP428, 38 more genes
nsv3918405	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 66,245,888-67,473,023 , NCBI36 chr16: 64,837,292-66,064,427 , GRCh37 chr16: 66,279,791-67,506,926	CDH16, PLEKHG4, 53 more genes
nsv3923505	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 65,285,584-66,456,849 , GRCh37 chr16: 66,728,083-67,899,348 , GRCh38 chr16: 66,694,180-67,865,445	CDH16, DYNC1LI2, 56 more genes
nsv3915173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636	RN7SL474P, UNC5D, 2109 more genes
nsv3901821	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028	TBC1D31, LOC105375740, 2109 more genes
nsv4349554	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385	LOC101929488, TEX15, 2105 more genes
nsv3916777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575	RPL5P22, ARHGEF10, 2105 more genes
nsv3898123	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385	SPAG1, LOC101927657, 2105 more genes
nsv3908608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028	LINC01617, PENK-AS1, 2105 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 84

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Number of Variants: 20

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