vegfa[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
nsv3921640	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr6: 43,855,142-43,858,554 , GRCh38 chr6: 43,779,427-43,782,839 , GRCh37 chr6: 43,747,164-43,750,576	VEGFA
nsv3919521	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 37,853,123-45,729,558 , GRCh37 chr6: 37,745,145-45,621,580 , GRCh38 chr6: 37,777,369-45,653,843	VEGFA, RPL23P6, 184 more genes
nsv3884243	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 43,636,308-50,947,320 , GRCh38.p12 chr6: 43,668,571-50,979,607	VEGFA, GLYATL3, 105 more genes
nsv3912856	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 41,713,777-46,588,645 , GRCh38 chr6: 41,638,061-46,512,949 , GRCh37 chr6: 41,605,799-46,480,686	VEGFA, PTCRA, 121 more genes
nsv3919402	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 42,769,519-46,417,784 , GRCh37.p13 chr6: 42,661,541-46,309,825 , GRCh38.p12 chr6: 42,693,803-46,342,088	VEGFA, LOC101929770, 94 more genes
nsv7097826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 41,126,341-43,752,536 , GRCh38.p12 chr6: 41,158,603-43,784,799	VEGFA, USP49, 96 more genes
nsv3924318	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 42,336,296-44,558,281 , NCBI36 chr6: 42,444,274-44,666,259 , GRCh38 chr6: 42,368,558-44,590,544	VEGFA, MIR4642, 82 more genes
nsv5673766	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 42,928,506-43,737,486 , GRCh38.p12 chr6: 42,960,768-43,769,749	VEGFA, SRF, 39 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	VEGFA, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	VEGFA, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	VEGFA, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	VEGFA, ITPR3, 2905 more genes
nsv4350067	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650	VEGFA, HLA-DPB2, 1001 more genes
nsv3913920	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028	VEGFA, TRR-ACG1-2, 1385 more genes
nsv6314749	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313	VEGFA, ACTG1P9, 245 more genes
nsv3913481	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr6: 43,732,603-44,458,145 , GRCh38 chr6: 43,656,888-44,382,430 , GRCh37 chr6: 43,624,625-44,350,167	VEGFA, LOC105375072, 26 more genes
nsv7097331	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 42,162,409-44,154,249 , GRCh38.p12 chr6: 42,194,671-44,186,512	VEGFA, MRPS10, 70 more genes
nsv7097825	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 41,126,341-43,737,486 , GRCh38.p12 chr6: 41,158,603-43,769,749	VEGFA, DNPH1, 96 more genes
nsv6636332	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 43,571,555-44,154,599 , GRCh38.p12 chr6: 43,603,818-44,186,862	VEGFA, CAPN11, 18 more genes
nsv3922186	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 43,613,072-43,860,167 , GRCh38 chr6: 43,537,357-43,784,452 , GRCh37 chr6: 43,505,094-43,752,189	VEGFA, MRPS18A, 8 more genes

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Items: 20

Number of Variants: 20

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