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

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6291587	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 3,501,624-5,357,124 , GRCh38.p12 chr19: 3,501,626-5,357,113	MYDGF, RN7SL202P, 67 more genes
nsv4350537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 3,076,808-4,796,782 , GRCh38.p12 chr19: 3,076,810-4,796,770	MYDGF, FEM1A, 70 more genes
nsv3915152	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 3,289,022-4,784,151 , GRCh38 chr19: 3,338,024-4,833,139 , GRCh37 chr19: 3,338,022-4,833,151	MYDGF, APBA3, 63 more genes
nsv3910627	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 3,554,633-4,690,977 , NCBI36 chr19: 3,505,633-4,641,977 , GRCh38 chr19: 3,554,635-4,690,965	MYDGF, PIAS4, 49 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	MYDGF, 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	MYDGF, 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	MYDGF, LENG8, 2408 more genes
nsv3914351	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555	MYDGF, SEMA6B, 299 more genes
nsv3924102	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622	MYDGF, POLR2E, 283 more genes
nsv3890584	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 3,120,160-9,732,820 , GRCh38.p12 chr19: 3,120,162-9,622,144	MYDGF, PCP2, 250 more genes
nsv4457776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345	MYDGF, BSG, 217 more genes
nsv3923561	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 184,565-4,650,484 , GRCh37 chr19: 233,565-4,699,484 , GRCh38 chr19: 233,565-4,699,472	MYDGF, DAPK3, 214 more genes
nsv3923885	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 4,008,560-4,763,159 , GRCh37 chr19: 4,008,558-4,763,171 , NCBI36 chr19: 3,959,558-4,714,171	MYDGF, MIR4746, 30 more genes
nsv3918318	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr19: 3,739,725-5,098,365 , GRCh37 chr19: 3,788,725-5,147,365 , GRCh38 chr19: 3,788,727-5,147,354	MYDGF, DAPK3, 49 more genes
nsv3910993	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr19: 3,031,619-4,863,634 , GRCh37 chr19: 3,080,619-4,912,634 , GRCh38 chr19: 3,080,621-4,912,622	MYDGF, DAPK3, 74 more genes
nsv3921377	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr19: 4,368,983-4,672,878 , GRCh38 chr19: 4,417,986-4,721,866 , GRCh37 chr19: 4,417,983-4,721,878	MYDGF, MIR4746, 13 more genes
nsv7095297	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777	MYDGF, NCLN, 223 more genes
nsv7095226	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377	MYDGF, ATP5F1D, 204 more genes
nsv3921092	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr19: 3,947,934-5,196,676 , GRCh37 chr19: 3,947,932-5,196,687 , NCBI36 chr19: 3,898,932-5,147,687	MYDGF, FEM1A, 43 more genes

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