3-Mercapto-n-nonylpropionamide - 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
nsv6311690	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 38,591,802-38,674,808 , GRCh38.p12 chr3: 38,550,311-38,633,317	SCN5A
nsv6311984	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 38,616,768-38,649,725 , GRCh38.p12 chr3: 38,575,277-38,608,234	SCN5A
nsv7097192	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 38,606,513-38,627,513 , GRCh38.p12 chr3: 38,565,022-38,586,022	SCN5A
nsv6314813	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 10,133,996-10,152,871 , GRCh37.p13 chr3: 10,175,680-10,194,555	VHL
nsv6289811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 10,170,715-10,188,894 , GRCh38.p12 chr3: 10,129,031-10,147,210	VHL
nsv4685893	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 37,038,201-37,053,310 , GRCh38.p12 chr3: 36,996,710-37,011,819	MLH1
nsv6289922	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 10,175,778-10,190,168 , GRCh38.p12 chr3: 10,134,094-10,148,484	VHL
nsv6289830	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 10,189,323-10,202,010 , GRCh38.p12 chr3: 10,147,639-10,160,326	VHL
nsv1398550	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 36,998,269-37,010,949 , GRCh37 chr3: 37,039,760-37,052,440	MLH1
nsv6289943	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 10,175,844-10,187,969 , GRCh38.p12 chr3: 10,134,160-10,146,285	VHL
nsv6289892	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 10,189,293-10,201,409 , GRCh38.p12 chr3: 10,147,609-10,159,725	VHL
nsv3880334	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 10,141,635-10,153,670 , GRCh37.p13 chr3: 10,183,319-10,195,354	VHL
nsv6289874	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 10,188,894-10,200,033 , GRCh38.p12 chr3: 10,147,210-10,158,349	VHL
nsv6289907	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 10,179,846-10,190,051 , GRCh38.p12 chr3: 10,138,162-10,148,367	VHL
nsv6289980	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 10,180,085-10,190,286 , GRCh38.p12 chr3: 10,138,401-10,148,602	VHL
nsv5200353	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 10,190,251-10,200,086 , GRCh38 chr3: 10,148,567-10,158,402	VHL
nsv5200351	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 10,190,210-10,200,045 , GRCh38 chr3: 10,148,526-10,158,361	VHL
nsv5200332	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 10,190,114-10,199,947 , GRCh38 chr3: 10,148,430-10,158,263	VHL
nsv5200342	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 10,180,892-10,190,625 , GRCh38 chr3: 10,139,208-10,148,941	VHL
nsv5673632	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 37,003,589-37,013,145 , GRCh37 chr3: 37,045,080-37,054,636	MLH1

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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

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Items: 1 to 20 of 17364

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Number of Variants: 20

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Supplemental Content

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