dbVar for Gene (Select 100312854) - dbVar - NCBI

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Items: 7

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Number of Variants: 7

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3417556	copy number variation	13	nstd162	human		GRCh37.p13 chrUn\|NT_167214.1: 51,901-70,800 , GRCh38 chrUn\|NT_167214.1: 51,901-70,800	VN1R112P
nsv481220	novel sequence insertion	1	nstd35	human		GRCh37.p13 chrUn\|NT_167214.1: 58,313-59,156 , GRCh38.p12 chr21\|NT_187305.1: 35,337-36,180 , GRCh38.p12 chr21\|NT_187314.1: 11,982-12,825 , GRCh38.p12 chr21\|NT_187317.1: 58,993-59,836 , GRCh38.p12 chr21\|NT_187318.1: 30,906-31,749 , GRCh38.p12 chr22\|NT_187388.1: 75,251-76,094 , GRCh38.p12 chrUn\|NT_167214.1: 58,313-59,156 , chr: 459-1,302 , GRCh38.p12 chr21\|NT_187304.1: 83,166-84,009	VN1R112P
nsv481108	novel sequence insertion	1	nstd35	human		GRCh37.p13 chrUn\|NT_167214.1: 55,634-58,330 , GRCh38.p12 chr21\|NT_187304.1: 80,477-83,183 , GRCh38.p12 chr21\|NT_187305.1: 32,648-35,354 , GRCh38.p12 chr21\|NT_187314.1: 12,808-15,514 , GRCh38.p12 chr21\|NT_187317.1: 56,304-59,010 , GRCh38.p12 chr21\|NT_187318.1: 28,217-30,923 , GRCh38.p12 chr22\|NT_187388.1: 72,562-75,268 , GRCh38.p12 chrUn\|NT_167214.1: 55,634-58,330	VN1R112P
nsv480709	novel sequence insertion	1	nstd35	human		GRCh37.p13 chrUn\|NT_167214.1: 57,328-58,197 , GRCh38.p12 chr21\|NT_187304.1: 82,171-83,050 , GRCh38.p12 chr21\|NT_187305.1: 34,342-35,221 , GRCh38.p12 chr21\|NT_187314.1: 12,941-13,820 , GRCh38.p12 chr21\|NT_187317.1: 57,998-58,877 , GRCh38.p12 chr21\|NT_187318.1: 29,911-30,790 , GRCh38.p12 chr22\|NT_187388.1: 74,256-75,135 , GRCh38.p12 chrUn\|NT_167214.1: 57,328-58,197	VN1R112P
nsv480080	novel sequence insertion	1	nstd35	human		GRCh37.p13 chrUn\|NT_167214.1: 57,306-58,187 , GRCh38.p12 chr21\|NT_187304.1: 82,149-83,040 , GRCh38.p12 chr21\|NT_187305.1: 34,320-35,211 , GRCh38.p12 chr21\|NT_187314.1: 12,951-13,842 , GRCh38.p12 chr21\|NT_187317.1: 57,976-58,867 , GRCh38.p12 chr21\|NT_187318.1: 29,889-30,780 , GRCh38.p12 chr22\|NT_187388.1: 74,234-75,125 , GRCh38.p12 chrUn\|NT_167214.1: 57,306-58,187	VN1R112P
nsv479916	novel sequence insertion	1	nstd35	human		GRCh37.p13 chrUn\|NT_167214.1: 59,195-60,576 , chr: 1,341-2,722 , GRCh38.p12 chr21\|NT_187304.1: 84,048-85,429 , GRCh38.p12 chr21\|NT_187305.1: 36,219-37,600 , GRCh38.p12 chr21\|NT_187317.1: 59,875-61,256 , GRCh38.p12 chr21\|NT_187318.1: 31,788-33,169 , GRCh38.p12 chr22\|NT_187388.1: 76,133-77,514 , GRCh38.p12 chrUn\|NT_167214.1: 59,195-60,576	VN1R112P
nsv479364	novel sequence insertion	1	nstd35	human		GRCh38.p12 chr21\|NT_187305.1: 32,425-34,287 , GRCh38.p12 chr21\|NT_187314.1: 13,875-15,737 , GRCh38.p12 chr21\|NT_187317.1: 56,081-57,943 , GRCh38.p12 chr21\|NT_187318.1: 27,994-29,856 , GRCh38.p12 chr22\|NT_187388.1: 72,339-74,201 , GRCh38.p12 chrUn\|NT_167214.1: 55,411-57,273 , GRCh37.p13 chrUn\|NT_167214.1: 55,411-57,273 , chr: 845-2,707 , GRCh38.p12 chr21\|NT_187304.1: 80,254-82,116	VN1R112P

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