OSC7395 AND nstd224 - dbVar - NCBI

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Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6625091	copy number variation	291	nstd224	human		GRCh37 chr1: 110,228,505-110,241,385 , GRCh38.p12 chr1: 109,685,883-109,698,763	GSTM1
nsv6628033	copy number variation	112	nstd224	human		GRCh37 chr2: 242,867,913-243,007,368 , GRCh38.p12 chr2: 241,925,762-242,065,217 , GRCh38.p12 chr2\|NT_187523.1: 1-109,287 , GRCh38.p12 chr2\|NT_187647.1: 1-108,927	LINC01238, LINC01880, 3 more genes
nsv6627234	copy number variation	26	nstd224	human		GRCh37 chr2: 110,852,875-110,983,320 , GRCh38.p12 chr2: 110,095,298-110,225,743	NPHP1, MALL, 2 more genes
nsv6621319	copy number variation	16	nstd224	human		GRCh37 chr12: 19,484,434-19,573,650 , GRCh38.p12 chr12: 19,331,500-19,420,716	PDCD5P1, PLEKHA5, 1 more genes
nsv6628246	copy number variation	29	nstd224	human		GRCh37 chr3: 100,355,338-100,441,859 , GRCh38.p12 chr3: 100,636,494-100,723,015	TFG, ADGRG7, 1 more genes
nsv6623458	copy number variation	2	nstd224	human		GRCh37 chr16: 32,523,490-32,592,826 , GRCh38.p12 chr16: 32,512,169-32,581,505	0
nsv6631082	copy number variation	194	nstd224	human		GRCh37 chr6: 67,017,494-67,044,618 , GRCh38.p12 chr6: 66,307,601-66,334,725	0
nsv6627377	copy number variation	4	nstd224	human		GRCh37 chr22: 24,324,016-24,386,612 , GRCh38.p12 chr22\|NT_187633.1: 218,191-280,787	GSTT1, GSTT2, 7 more genes
nsv6625225	copy number variation	2	nstd224	human		GRCh37 chr19: 52,272,131-52,617,369 , GRCh38.p12 chr19: 51,768,878-52,114,116	FPR3, ZNF615, 17 more genes
nsv6623664	copy number variation	56	nstd224	human		GRCh37 chr16: 34,489,371-34,732,946 , GRCh38.p12 chr16: 35,255,000-35,498,575	LINC01566, AGGF1P9, 21 more genes

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