M2221 AND nstd157 - dbVar - NCBI

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3317248	copy number variation	18	nstd157	human		GRCh37 chr5: 97,048,466-97,096,042 , GRCh38.p12 chr5: 97,712,762-97,760,338	LOC391813
nsv3317959	copy number variation	4	nstd157	human		GRCh37 chr12: 99,994,315-100,008,773 , GRCh38.p12 chr12: 99,600,537-99,614,995	ANKS1B
nsv3317836	copy number variation	19	nstd157	human		GRCh37 chr18: 67,208,806-67,217,271 , GRCh38.p12 chr18: 69,541,570-69,550,035	DOK6
nsv3317223	copy number variation	4	nstd157	human		GRCh38.p12 chr16: 75,530,389-75,544,521 , GRCh37 chr16: 75,564,287-75,578,419	CHST5, TMEM231
nsv3318209	copy number variation	2	nstd157	human		GRCh37 chr5: 816,753-824,025 , GRCh38.p12 chr5: 816,638-823,910	ZDHHC11, SPCS2P3
nsv3318809	copy number variation	11	nstd157	human		GRCh38.p12 chr10: 133,429,369-133,567,018 , GRCh37 chr10: 135,242,873-135,380,522	CYP2E1, OR7M1P, 7 more genes
nsv3318316	copy number variation	72	nstd157	human		GRCh37 chr14: 41,615,868-41,661,685 , GRCh38.p12 chr14: 41,146,665-41,192,482	0
nsv3318308	copy number variation	19	nstd157	human		GRCh37 chr16: 19,945,540-19,962,636 , GRCh38.p12 chr16: 19,934,218-19,951,314	0
nsv3317878	copy number variation	25	nstd157	human		GRCh37 chr3: 162,131,408-162,142,475 , GRCh38.p12 chr3: 162,413,620-162,424,687	0
nsv3318039	copy number variation	18	nstd157	human		GRCh37 chr13: 58,589,893-58,599,174 , GRCh38.p12 chr13: 58,015,759-58,025,040	0
nsv3318303	copy number variation	8	nstd157	human		GRCh37 chr8: 15,778,007-15,786,889 , GRCh38.p12 chr8: 15,920,498-15,929,380	0

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M2221 AND nstd157 (12)
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