M2225 AND nstd157 - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3317883	copy number variation	1	nstd157	human		GRCh37 chr6: 162,912,514-162,962,828 , GRCh38.p12 chr6: 162,491,482-162,541,796	PRKN
nsv3318353	copy number variation	3	nstd157	human		GRCh37 chr16: 79,260,765-79,273,682 , GRCh38.p12 chr16: 79,226,868-79,239,785	MAF
nsv3318458	copy number variation	16	nstd157	human		GRCh37 chr8: 16,262,222-16,272,444 , GRCh38.p12 chr8: 16,404,713-16,414,935	LOC101929028
nsv3318957	copy number variation	1	nstd157	human		GRCh37 chr15: 24,203,933-24,213,615 , GRCh38.p12 chr15: 23,958,786-23,968,468	LOC107984787
nsv3317763	copy number variation	17	nstd157	human		GRCh37 chr18: 66,746,208-66,755,736 , GRCh38.p12 chr18: 69,078,971-69,088,499	CCDC102B
nsv3317807	copy number variation	1	nstd157	human		GRCh37 chr9: 72,036,369-72,048,983 , GRCh38.p12 chr9: 69,421,453-69,434,067	APBA1
nsv3318191	copy number variation	3	nstd157	human		GRCh38.p12 chr10: 44,713,993-44,864,035 , GRCh37 chr10: 45,209,441-45,359,483	TMEM72-AS1, EIF2AP4
nsv3317846	copy number variation	16	nstd157	human		GRCh38.p12 chr9: 133,071,778-133,082,065 , GRCh37 chr9: 135,947,165-135,957,452	CEL, CELP
nsv3318927	copy number variation	12	nstd157	human		GRCh37 chr3: 151,514,590-151,549,959 , GRCh38.p12 chr3: 151,796,802-151,832,171	AADAC, AADACL2-AS1, 1 more genes
nsv3317916	copy number variation	17	nstd157	human		GRCh38.p12 chr15: 25,179,434-25,185,507 , GRCh37 chr15: 25,424,581-25,430,654	SNORD115-6, SNORD115-7, 3 more genes
nsv3317851	copy number variation	1	nstd157	human		GRCh38.p12 chr12: 7,845,083-7,970,710 , GRCh37 chr12: 7,997,679-8,123,306	SLC2A3, SLC2A14, 3 more genes
nsv3318099	copy number variation	13	nstd157	human		GRCh37 chr2: 89,616,271-90,248,037 , GRCh38.p12 chr2: 89,316,513-90,209,171	ABCD1P1, IGKV6D-41, 40 more genes
nsv3318549	copy number variation	16	nstd157	human		GRCh38.p12 chr: NaN-NaN , GRCh37 chr20: 29,652,403-29,842,291	0
nsv3318838	copy number variation	1	nstd157	human		GRCh37 chr20: 55,406,875-55,428,048 , GRCh38.p12 chr20: 56,831,819-56,852,992	0
nsv3317289	copy number variation	24	nstd157	human		GRCh37 chr9: 24,502,737-24,518,795 , GRCh38.p12 chr9: 24,502,739-24,518,797	0
nsv3318427	copy number variation	34	nstd157	human		GRCh37 chr11: 81,501,218-81,517,261 , GRCh38.p12 chr11: 81,790,176-81,806,219	0
nsv3318499	copy number variation	1	nstd157	human		GRCh37 chr21: 42,291,798-42,299,657 , GRCh38.p12 chr21: 40,919,872-40,927,731	0
nsv3318502	copy number variation	31	nstd157	human		GRCh37 chr9: 78,004,378-78,011,616 , GRCh38.p12 chr9: 75,389,462-75,396,700	0
nsv3317267	copy number variation	2	nstd157	human		GRCh37 chr13: 62,621,651-62,626,953 , GRCh38.p12 chr13: 62,047,518-62,052,820	0

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