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

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3891016	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 49,447,713-49,470,073 , GRCh38.p12 chr19: 48,944,456-48,966,816	DHDH, BAX, 2 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	DHDH, 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	DHDH, 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	DHDH, LENG8, 2408 more genes
nsv3919076	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 48,432,832-59,083,573 , NCBI36 chr19: 53,124,644-63,775,385 , GRCh38 chr19: 47,929,575-58,572,206	DHDH, KCNA7, 697 more genes
nsv3911950	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 48,411,797-59,051,332 , NCBI36 chr19: 53,103,609-63,743,144 , GRCh38 chr19: 47,908,540-58,539,965	DHDH, LOC107987270, 694 more genes
nsv4676357	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308	DHDH, MIR4324, 485 more genes
nsv4729755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886	DHDH, SIGLEC5, 574 more genes
nsv3918983	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 46,658,791-49,050,450 , GRCh37 chr19: 47,162,048-49,553,707 , NCBI36 chr19: 51,853,888-54,245,519	DHDH, LOC105372432, 121 more genes
nsv3899618	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 49,389,934-49,477,474 , GRCh38.p12 chr19: 48,886,677-48,974,217	DHDH, BAX, 5 more genes
nsv4685764	copy number variation	1	nstd102	human	not provided	GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460	DHDH, SNAR-G1, 453 more genes
nsv4457853	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 48,119,589-49,595,956 , GRCh38.p12 chr19: 47,616,332-49,092,699	DHDH, GRIN2D, 94 more genes

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