dbVar for Nucleotide (Select 224183269) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location
nsv5671860	copy number variation	1	nstd207	human	GRCh38 chrUn\|GL000220.1: 119,368-119,471
nsv5671295	copy number variation	1	nstd207	human	GRCh38 chrUn\|GL000220.1: 135,646-135,698
nsv5670770	copy number variation	1	nstd207	human	GRCh38 chrUn\|GL000220.1: 45,590-45,650
nsv5670481	copy number variation	1	nstd207	human	GRCh38 chrUn\|GL000220.1: 97,699-97,908
nsv5670094	copy number variation	1	nstd207	human	GRCh38 chrUn\|GL000220.1: 119,164-119,879
nsv5668458	copy number variation	1	nstd207	human	GRCh38 chrUn\|GL000220.1: 133,443-133,518
nsv5667180	copy number variation	1	nstd207	human	GRCh38 chrUn\|GL000220.1: 148,083-148,261
nsv5665188	copy number variation	1	nstd207	human	GRCh38 chrUn\|GL000220.1: 102,603-102,682
nsv5620577	insertion	2	nstd207	human	GRCh38 chrUn\|GL000220.1: 119,111-119,111
nsv5615436	insertion	1	nstd207	human	GRCh38 chrUn\|GL000220.1: 146,088-146,088
nsv5615213	insertion	1	nstd207	human	GRCh38 chrUn\|GL000220.1: 132,963-132,963
nsv5610437	insertion	1	nstd207	human	GRCh38 chrUn\|GL000220.1: 134,023-134,023
nsv5608565	insertion	1	nstd207	human	GRCh38 chrUn\|GL000220.1: 119,606-119,606
nsv5607298	insertion	1	nstd207	human	GRCh38 chrUn\|GL000220.1: 102,547-102,547
nsv5600783	insertion	1	nstd207	human	GRCh38 chrUn\|GL000220.1: 15,220-15,220
nsv3951298	copy number variation	1	nstd167	human	GRCh37 chrUn\|GL000220.1: 45,590-45,651
nsv3950964	copy number variation	1	nstd167	human	GRCh37 chrUn\|GL000220.1: 102,077-102,124
nsv3939808	insertion	1	nstd167	human	GRCh37 chrUn\|GL000220.1: 119,111-119,111
nsv3927016	insertion	1	nstd167	human	GRCh37 chrUn\|GL000220.1: 125,575-125,575
nsv3925142	insertion	1	nstd167	human	GRCh37 chrUn\|GL000220.1: 13,059-13,059

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Items: 20

Number of Variants: 20

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