dbVar for Gene (Select 4573) - 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
nsv7098831	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrMT: 10,947-15,537 , GRCh38 chrMT: 10,947-15,537	TRNS2, TRNP, 10 more genes
nsv5674222	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrMT: 7,126-13,988 , GRCh37 chrMT: 7,126-13,988	TRNH, ND6, 20 more genes
nsv5674221	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrMT: 6,468-15,586 , GRCh37 chrMT: 6,468-15,586	ND5, TRNG, 20 more genes
nsv5674171	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrMT: 10,105-15,066 , GRCh38 chrMT: 10,105-15,066	COX3, ND3, 13 more genes
nsv5674154	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrMT: 8,585-12,965 , GRCh38 chrMT: 8,585-12,965	ATP6, TRNL2, 15 more genes
nsv5674153	copy number variation	2	nstd102	human	not provided, Pathogenic	GRCh37 chrMT: 8,470-13,446 , GRCh38 chrMT: 8,470-13,446	ND4, ND6, 15 more genes
nsv4685968	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrMT: 8,839-14,895 , GRCh38 chrMT: 8,839-14,895	TRNG, TRNK, 16 more genes
nsv4685966	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrMT: 5,794-14,876 , GRCh38 chrMT: 5,794-14,876	ATP6, ATP8, 26 more genes
nsv4685959	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrMT: 8,290-13,040 , GRCh37 chrMT: 8,290-13,040	CYTB, ND4L, 15 more genes
nsv4685954	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrMT: 8,480-13,440 , GRCh37 chrMT: 8,480-13,440	COX2, TRNE, 15 more genes
nsv4685933	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrMT: 8,815-13,722 , GRCh38 chrMT: 8,815-13,722	CYTB, ND6, 14 more genes
nsv4685928	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrMT: 6,003-11,220 , GRCh37 chrMT: 6,003-11,220	COX2, ND4L, 21 more genes
nsv4685910	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrMT: 8,350-13,450 , GRCh38 chrMT: 8,350-13,450	TRNK, TRNG, 15 more genes
nsv4685892	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrMT: 7,730-11,255 , GRCh38 chrMT: 7,730-11,255	TRNG, TRNK, 15 more genes
nsv4685879	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrMT: 5,782-13,922 , GRCh38 chrMT: 5,782-13,922	ATP6, ATP8, 25 more genes
esv2577495	copy number variation	1	estd197	human		GRCh37.p13 chrMT: 10,819-10,819 , GRCh38.p12 chrMT: 10,819-10,819 , NCBI36 chrMT: 10,820-10,820	ND3, ND4, 6 more genes
esv2558572	insertion	1	estd197	human		GRCh37.p13 chrMT: 8,661-8,661 , GRCh38.p12 chrMT: 8,661-8,661 , NCBI36 chrMT: 8,662-8,662	ATP6, ATP8, 7 more genes
esv2458774	insertion	1	estd197	human		GRCh37.p13 chrMT: 9,353-9,353 , GRCh38.p12 chrMT: 9,353-9,353 , NCBI36 chrMT: 9,354-9,354	ATP6, COX3, 5 more genes
esv2486261	insertion	1	estd197	human		GRCh37.p13 chrMT: 9,581-9,581 , GRCh38.p12 chrMT: 9,581-9,581 , NCBI36 chrMT: 9,582-9,582	ATP6, COX3, 5 more genes
esv2534046	insertion	1	estd197	human		GRCh37.p13 chrMT: 9,457-9,457 , GRCh38.p12 chrMT: 9,457-9,457 , NCBI36 chrMT: 9,458-9,458	ATP6, COX3, 5 more genes

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Number of Variants: 20

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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 33

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Number of Variants: 20

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