cc2d1a[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6634314	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 14,030,327-14,033,916 , GRCh38 chr19: 13,919,514-13,923,103	CC2D1A
nsv5673147	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr19: 14,023,543-14,032,892 , GRCh38 chr19: 13,912,730-13,922,079	CC2D1A
nsv3901120	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 14,040,911-14,044,158 , GRCh38.p12 chr19: 13,930,098-13,933,345	CC2D1A, PODNL1
nsv3924466	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,496,978-14,126,833 , GRCh38 chr19: 11,525,163-14,155,021 , GRCh37 chr19: 11,635,978-14,265,833	CC2D1A, JUNB, 135 more genes
nsv3912480	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 12,580,427-14,742,673 , GRCh37 chr19: 12,691,241-14,853,485 , NCBI36 chr19: 12,552,241-14,714,485	CC2D1A, GET3, 100 more genes
nsv3907864	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 12,574,343-14,726,197 , GRCh38.p12 chr19: 12,463,529-14,615,385	CC2D1A, WDR83, 105 more genes
nsv3910509	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 13,505,739-15,342,900 , GRCh37 chr19: 13,644,739-15,481,900 , GRCh38 chr19: 13,533,925-15,371,089	CC2D1A, DDX39A, 76 more genes
nsv6291633	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 12,697,728-14,111,313 , GRCh38.p12 chr19: 12,586,914-14,000,501	CC2D1A, RN7SL619P, 67 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	CC2D1A, 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	CC2D1A, 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	CC2D1A, 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	CC2D1A, BCKDHA, 1102 more genes
nsv3898900	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 9,678,768-14,853,426 , GRCh38.p12 chr19: 9,568,092-14,742,614	CC2D1A, FBXL12, 253 more genes
nsv3923415	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 10,286,934-14,020,806 , GRCh37 chr19: 10,425,934-14,159,806 , GRCh38 chr19: 10,315,258-14,048,994	CC2D1A, MAN2B1, 182 more genes
nsv3915094	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 12,132,052-14,751,798 , NCBI36 chr19: 12,103,867-14,723,610 , GRCh37 chr19: 12,242,867-14,862,610	CC2D1A, RN7SL619P, 123 more genes
nsv3891875	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr19: 13,592,592-14,717,528 , GRCh38.p12 chr19: 13,481,778-14,606,716	CC2D1A, CACNA1A, 48 more genes
nsv3913955	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 13,644,739-14,369,645 , GRCh38 chr19: 13,533,925-14,258,833 , NCBI36 chr19: 13,505,739-14,230,645	CC2D1A, YJU2B, 30 more genes
nsv3899944	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 11,608,072-14,543,046 , GRCh38.p12 chr19: 11,497,257-14,432,234	CC2D1A, RNA5SP465, 145 more genes

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