dbVar for Gene (Select 644906) - 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
nsv5564204	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr6: 15,523,206-16,146,982 , GRCh38.p12 chr6: 15,522,975-16,146,751	MDH1P2, LINC02543, 8 more genes
nsv4457139	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 14,715,955-17,223,929 , GRCh38.p12 chr6: 14,715,724-17,223,698	MDH1P2, ATXN1, 28 more genes
nsv4456780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393	LOC105374960, LOC101928573, 342 more genes
nsv4456299	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 13,910,125-22,000,204 , GRCh38.p12 chr6: 13,909,894-21,999,975	LOC101928354, MBOAT1, 101 more genes
nsv4455888	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 13,248,587-18,083,552 , GRCh38.p12 chr6: 13,248,355-18,083,321	RNU6-522P, LOC105374942, 70 more genes
nsv3922594	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 13,311,751-16,295,791 , GRCh38 chr6: 13,311,519-16,295,560 , NCBI36 chr6: 13,419,730-16,403,770	LOC107986571, LOC105374947, 47 more genes
nsv3922052	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 155,807-17,058,645 , NCBI36 chr6: 100,807-17,166,624 , GRCh38 chr6: 155,807-17,058,414	ECI2-DT, RNU1-11P, 268 more genes
nsv3921817	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 2,862,874-16,698,019 , GRCh38 chr6: 2,862,640-16,697,788 , NCBI36 chr6: 2,807,873-16,805,998	RN7SKP293, LOC105374906, 230 more genes
nsv3920564	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946	PRELID1P2, RPL7AP7, 785 more genes
nsv3915452	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr6: 14,838,766-17,662,301 , GRCh37 chr6: 14,730,787-17,554,322 , GRCh38 chr6: 14,730,556-17,554,091	GMPR, JARID2, 32 more genes
nsv3913920	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028	TRR-ACG1-2, TMEM217, 1385 more genes
nsv3913657	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 51,431-18,468,805 , GRCh38 chr6: 106,431-18,360,595 , GRCh37 chr6: 106,431-18,360,826	LOC105374904, CAP2, 294 more genes
nsv3909865	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 14,958,991-18,581,139 , NCBI36 chr6: 15,066,970-18,689,118 , GRCh38 chr6: 14,958,760-18,580,908	NUP153, JARID2-AS1, 53 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
nsv3888615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 168,775-24,023,234 , GRCh38.p12 chr6: 168,775-24,023,006	LOC107986557, PXDC1, 349 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
nsv3886069	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 156,974-21,955,964 , GRCh38.p12 chr6: 156,974-21,955,733	FOXCUT, ACCSLP1, 331 more genes
nsv3883690	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 8,269,414-17,402,660 , GRCh38.p12 chr6: 8,269,181-17,402,429	EDN1, GCNT2, 129 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
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

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Number of Variants: 20

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dbVar

Result Filters

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Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 104

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Number of Variants: 20

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