ccs[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
nsv7097086	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 74,189,435-74,363,609 , GRCh38.p12 chr6: 73,479,712-73,653,886	MTO1, RPS27P15, 3 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	CCS, FAUP4, 2031 more genes
nsv3924180	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 65,316,269-84,193,229 , GRCh38 chr6: 64,549,655-83,426,791 , GRCh37 chr6: 65,259,548-84,136,510	LOC105377875, KCNQ5-IT1, 188 more genes
nsv6315402	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 64,954,687-79,581,678 , GRCh38.p12 chr6: 64,244,794-78,871,961	LOC105377841, RPS6P8, 139 more genes
nsv3889959	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 73,674,612-84,829,774 , GRCh38.p12 chr6: 72,964,889-84,120,055	MRAP2, LCA5, 125 more genes
nsv6291322	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 72,799,054-83,275,894 , GRCh38.p12 chr6: 72,089,351-82,566,177	RPS27P15, COX7A2, 118 more genes
nsv6291339	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 70,165,296-79,920,769 , GRCh38.p12 chr6: 69,455,404-79,211,052	RNU6-84P, PGAM1P10, 113 more genes
nsv4729340	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 74,226,559-80,208,037 , GRCh38.p12 chr6: 73,516,836-79,498,320	LOC107986613, LOC101928516, 58 more genes
nsv6634377	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 71,105,038-75,200,617 , GRCh38.p12 chr6: 70,395,335-74,490,901	TXNP7, MTO1, 63 more genes
nsv3921639	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 65,265,478-67,229,716 , GRCh37 chr11: 65,508,902-67,473,140 , GRCh38 chr11: 65,741,431-67,705,669	CCS, MIR6860, 106 more genes
nsv5673923	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 72,596,727-74,363,609 , GRCh38.p12 chr6: 71,887,024-73,653,886	LOC100422453, RPS27P15, 32 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	LOC105378061, MIR4640, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	RNU6-411P, LOC107986611, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	SOD1P1, HLA-DPB1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	ITPR3, HSD17B8, 2905 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	CCS, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	CCS, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	CCS, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	CCS, PYGM, 2125 more genes
nsv4350067	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650	HLA-DPB2, CIMIP3, 1001 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 31

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Number of Variants: 20

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Supplemental Content

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Search details

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