cox7a1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3893829	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 36,606,538-36,643,669 , GRCh38.p12 chr19: 36,115,636-36,152,767	COX7A1, LOC105372385, 2 more genes
nsv3919296	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723	COX7A1, UBA2, 241 more genes
nsv3916007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990	COX7A1, MAG, 238 more genes
nsv4349605	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 35,111,811-37,744,992 , GRCh38.p12 chr19: 34,620,906-37,254,090	COX7A1, ATP4A, 129 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	COX7A1, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	COX7A1, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	COX7A1, LENG8, 2408 more genes
nsv3913730	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354	COX7A1, BCKDHA, 1102 more genes
nsv6290300	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324	COX7A1, ZNF420, 574 more genes
nsv4457372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575	COX7A1, ZNF461, 735 more genes
nsv3895284	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 36,628,463-36,758,139 , GRCh38.p12 chr19: 36,137,561-36,267,237	COX7A1, ZNF146, 4 more genes
nsv6310629	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 35,521,725-36,643,309 , GRCh38.p12 chr19: 35,030,821-36,152,407	COX7A1, KRTDAP, 78 more genes
nsv3902356	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 36,147,111-37,249,653 , GRCh38.p12 chr19: 35,656,209-36,758,751	COX7A1, RNY5P10, 56 more genes
nsv4457836	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 36,570,287-36,655,341 , GRCh38.p12 chr19: 36,079,385-36,164,439	COX7A1, OVOL3, 5 more genes
nsv7095478	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407	COX7A1, NFKBID, 141 more genes
nsv3909857	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 36,475,577-38,399,402 , GRCh38.p12 chr19: 35,984,675-37,908,762	COX7A1, ZNF790, 72 more genes

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cox7a1[All Fields] AND 1[has_clinical] (17)
dbVar
Nezumia liolepis[orgn] (27)
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