sod2[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
nsv3897813	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 160,085,434-160,088,254 , GRCh38.p12 chr6: 159,664,402-159,667,222	SOD2
nsv3908019	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 160,085,841-160,088,254 , GRCh38.p12 chr6: 159,664,809-159,667,222	SOD2
nsv3892404	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 160,086,661-160,088,418 , GRCh38.p12 chr6: 159,665,629-159,667,386	SOD2
nsv3912998	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr6: 159,598,794-159,726,489 , NCBI36 chr6: 159,939,816-160,067,511 , GRCh37 chr6: 160,019,826-160,147,521	SOD2, LOC105378085, 3 more genes
nsv3911475	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 152,793,402-170,610,394 , GRCh37 chr6: 153,114,537-170,919,482 , NCBI36 chr6: 153,156,230-170,761,407	SOD2, SNORA116, 275 more genes
nsv3913213	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 154,118,058-170,602,152 , NCBI36 chr6: 154,480,885-170,753,165 , GRCh37 chr6: 154,439,193-170,911,240	SOD2, LDHAL6FP, 258 more genes
nsv3921695	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 154,539,655-170,714,507 , NCBI36 chr6: 154,902,481-170,865,520 , GRCh37 chr6: 154,860,789-171,023,595	SOD2, LOC105378128, 255 more genes
nsv6315428	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 159,121,459-170,919,482 , GRCh38.p12 chr6: 158,700,427-170,610,394	SOD2, TBP, 200 more genes
nsv3921491	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 159,795,661-170,763,014 , GRCh38 chr6: 159,454,639-170,612,001 , GRCh37 chr6: 159,875,671-170,921,089	SOD2, LOC102724357, 183 more genes
nsv1397956	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 159,830,469-170,673,013 , GRCh37.p13 chr6: 159,910,479-170,831,088 , GRCh38.p12 chr6: 159,489,447-170,522,000	SOD2, LOC107986675, 179 more genes
nsv6313530	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 153,207,930-164,322,346 , GRCh38.p12 chr6: 152,886,795-163,901,314	SOD2, RSPH3, 144 more genes
nsv6634356	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 157,318,401-165,233,548 , GRCh38.p12 chr6: 156,997,267-164,820,059	SOD2, LOC105378097, 103 more genes
nsv3916251	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 155,378,049-163,133,499 , NCBI36 chr6: 155,740,875-163,474,521 , GRCh37 chr6: 155,699,183-163,554,531	SOD2, MAP3K4, 99 more genes
nsv7097050	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 158,532,398-162,868,359 , GRCh38.p12 chr6: 158,111,366-162,447,327	SOD2, LOC107986665, 64 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	SOD2, LOC105378061, 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	SOD2, RNU6-411P, 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	SOD2, SOD1P1, 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	SOD2, ITPR3, 2905 more genes
nsv3911993	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033	SOD2, LOC105369171, 418 more genes
nsv3920975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591	SOD2, UST-AS2, 394 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 35

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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