m6pr[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
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	SNORA116, PRR18, 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	LDHAL6FP, QKI, 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	LOC105378128, LOC105378102, 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	TBP, LOC105378130, 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	LOC102724357, LOC101929142, 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	LOC107986675, MPC1, 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	RSPH3, FBXO5, 144 more genes
nsv3918679	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 160,336,422-171,023,595 , NCBI36 chr6: 160,256,412-170,865,520 , GRCh38 chr6: 159,915,390-170,714,507	FAM120B, LOC107986672, 172 more genes
nsv3923088	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 160,246,945-170,921,089 , NCBI36 chr6: 160,166,935-170,763,014 , GRCh38 chr6: 159,825,913-170,612,001	DKFZp451B082, LOC107986548, 169 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	LOC105378097, LOC105378094, 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	MAP3K4, LOC112267977, 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	LOC107986665, HNRNPH1P1, 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	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
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	M6PR, RNA5SP369, 2454 more genes
nsv3905447	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316	M6PR, LOH12CR2, 2452 more genes
nsv3897722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059	M6PR, RNU4ATAC16P, 2452 more genes
nsv3914194	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807	M6PR, BTG1P1, 2451 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 68

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Number of Variants: 20

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