cox10[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
nsv3893225	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr17: 14,110,043-14,111,913 , GRCh38.p12 chr17: 14,206,726-14,208,596	COX10
nsv3891088	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 14,041,216-14,108,096 , GRCh38.p12 chr17: 14,137,899-14,204,779	COX10
nsv6310056	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr17: 14,110,107-14,110,530 , GRCh38.p12 chr17: 14,206,790-14,207,213	COX10
nsv3904161	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 14,098,277-14,190,782 , GRCh38.p12 chr17: 14,194,960-14,287,465	COX10, CDRT15
nsv4675628	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 13,933,395-14,055,324 , GRCh38.p12 chr17: 14,030,078-14,152,007	COX10, COX10-DT
nsv6310122	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 13,972,923-14,110,530 , GRCh38.p12 chr17: 14,069,606-14,207,213	COX10, COX10-DT
nsv4457482	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 13,879,079-14,013,128 , GRCh38.p12 chr17: 13,975,762-14,109,811	COX10, CDRT15P1, 1 more genes
nsv6291753	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 13,738,798-14,156,469 , GRCh38.p12 chr17: 13,835,481-14,253,152	COX10, COX10-DT, 3 more genes
nsv4348874	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 14,104,012-15,551,814 , GRCh38.p12 chr17: 14,200,695-15,648,500	COX10, MIR4731, 26 more genes
nsv6637466	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 14,077,819-15,491,532 , GRCh38.p12 chr17: 14,174,502-15,588,218	COX10, RPL23AP76, 25 more genes
nsv3922449	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr17: 14,014,328-15,423,498 , GRCh37.p13 chr17: 14,073,603-15,482,773 , GRCh38.p12 chr17: 14,170,286-15,579,459	COX10, PMP22, 25 more genes
nsv3918082	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 14,028,658-15,432,257 , GRCh37 chr17: 14,087,933-15,491,532 , GRCh38 chr17: 14,184,616-15,588,218	COX10, MIR4731, 25 more genes
nsv6637617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 14,087,934-15,491,532 , GRCh38.p12 chr17: 14,184,617-15,588,218	COX10, MGC12916, 25 more genes
nsv3915951	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 14,087,787-15,490,100 , NCBI36 chr17: 14,028,512-15,430,825 , GRCh38 chr17: 14,184,470-15,586,786	COX10, RNU6-799P, 25 more genes
nsv3905267	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 14,098,660-15,500,645 , GRCh38.p12 chr17: 14,195,343-15,597,331	COX10, TVP23C, 25 more genes
nsv6637838	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 14,082,945-15,484,858 , GRCh38.p12 chr17: 14,179,628-15,581,544	COX10, FBXW10B, 25 more genes
nsv6637965	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 14,083,055-15,484,859 , GRCh38.p12 chr17: 14,179,738-15,581,545	COX10, CDRT8, 25 more genes
nsv6637613	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 14,087,788-15,484,858 , GRCh38.p12 chr17: 14,184,471-15,581,544	COX10, TVP23C-CDRT4, 25 more genes
nsv3924098	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 14,087,933-15,484,858 , GRCh38 chr17: 14,184,616-15,581,544	COX10, CDRT4, 25 more genes
nsv3902390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 14,087,933-15,484,858 , GRCh38.p12 chr17: 14,184,616-15,581,544	COX10, MIR4731, 25 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

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Items: 1 to 20 of 100

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Number of Variants: 20

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