aldh3a2[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
nsv4449732	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 19,552,275-19,578,895 , GRCh38 chr17: 19,648,962-19,675,582	ALDH3A2
nsv7095134	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 19,552,285-19,561,195 , GRCh38.p12 chr17: 19,648,972-19,657,882	ALDH3A2
nsv5672871	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 19,552,275-19,561,185 , GRCh38.p12 chr17: 19,648,962-19,657,872	ALDH3A2
nsv4684260	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 19,552,285-19,561,175 , GRCh38.p12 chr17: 19,648,972-19,657,862	ALDH3A2
nsv7094863	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 19,559,659-19,568,380 , GRCh38.p12 chr17: 19,656,346-19,665,067	ALDH3A2
nsv5672959	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 19,552,275-19,555,955 , GRCh38.p12 chr17: 19,648,962-19,652,642	ALDH3A2
nsv6310058	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 19,564,430-19,566,822 , GRCh38.p12 chr17: 19,661,117-19,663,509	ALDH3A2
nsv7095081	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 19,554,850-19,555,955 , GRCh38.p12 chr17: 19,651,537-19,652,642	ALDH3A2
nsv7095135	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 19,575,024-19,575,279 , GRCh38.p12 chr17: 19,671,711-19,671,966	ALDH3A2
nsv4682696	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 19,566,636-19,566,822 , GRCh38.p12 chr17: 19,663,323-19,663,509	ALDH3A2
nsv7094960	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 19,564,420-19,564,601 , GRCh38.p12 chr17: 19,661,107-19,661,288	ALDH3A2
nsv3916690	delins	1	nstd102	human	Pathogenic	GRCh38 chr17: 19,649,129-19,652,139 , GRCh37.p13 chr17: 19,552,442-19,555,452	ALDH3A2
nsv6310129	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 19,575,024-19,578,895 , GRCh38.p12 chr17: 19,671,711-19,675,582	ALDH3A2
nsv6310046	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr17: 19,656,258-19,656,259 , GRCh37 chr17: 19,559,571-19,559,572	ALDH3A2
nsv4675203	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 19,574,666-19,624,308 , GRCh38.p12 chr17: 19,671,353-19,720,995	ALDH3A2, SLC47A2
nsv6291691	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 19,559,095-19,708,057 , GRCh38.p12 chr17: 19,655,782-19,804,744	ALDH3A2, ALDH3A1, 3 more genes
nsv3891583	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 19,494,823-19,563,018 , GRCh38.p12 chr17: 19,591,510-19,659,705	ALDH3A2, NMTRQ-TTG12-1, 4 more genes
nsv3890462	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 17,200,426-21,900,910 , GRCh38.p12 chr17: 17,297,112-22,374,304	ALDH3A2, LOC100132977, 179 more genes
nsv3919368	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 15,704,477-20,556,000 , GRCh37.p13 chr17: 15,763,752-20,615,408 , GRCh38.p12 chr17: 15,860,438-20,712,095	ALDH3A2, CCDC144A, 196 more genes
nsv3910522	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 15,754,173-20,552,548 , GRCh38 chr17: 15,850,859-20,649,235 , NCBI36 chr17: 15,694,898-20,493,140	ALDH3A2, EEF1A1P43, 196 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

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Items: 1 to 20 of 134

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Number of Variants: 20

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