OSC7620 AND nstd224 - dbVar - NCBI

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Items: 11

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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
nsv6630814	copy number variation	62	nstd224	human		GRCh37 chr5: 97,051,856-97,096,042 , GRCh38.p12 chr5: 97,716,152-97,760,338	LOC391813
nsv6629898	copy number variation	832	nstd224	human		GRCh37 chr4: 69,401,172-69,435,811 , GRCh38.p12 chr4: 68,535,454-68,570,093	UGT2B17
nsv6633178	copy number variation	15	nstd224	human		GRCh37 chr9: 17,585,896-17,633,023 , GRCh38.p12 chr9: 17,585,898-17,633,025	PABPC1P11, SH3GL2
nsv6634207	copy number variation	6	nstd224	human		GRCh37 chrX: 134,756,293-134,911,512 , GRCh38.p12 chrX: 135,622,368-135,743,081	SAGE4P, SAGE2P, 3 more genes
nsv6628142	copy number variation	2	nstd224	human		GRCh37 chr2: 75,164,700-75,233,994 , GRCh38.p12 chr2: 74,937,573-75,006,867	POLE4, LINC01293, 2 more genes
nsv6626922	copy number variation	25	nstd224	human		GRCh37 chr22: 24,301,973-24,390,432 , GRCh38.p12 chr22\|NT_187633.1: 196,148-284,607	GSTT1, MTND1P13, 10 more genes
nsv6622325	copy number variation	13	nstd224	human		GRCh37 chr13: 70,744,882-70,773,605 , GRCh38.p12 chr13: 70,170,750-70,199,473	0
nsv6624084	copy number variation	158	nstd224	human		GRCh37 chr17: 44,179,983-44,353,222 , GRCh38.p12 chr17: 46,102,617-46,275,856 , GRCh38.p12 chr17\|NT_187663.1: 804,722-954,783	KANSL1, KANSL1-AS1, 5 more genes
nsv6620384	copy number variation	8	nstd224	human		GRCh37 chr10: 46,980,871-47,703,869 , GRCh38.p12 chr10: 46,157,935-47,923,579	BMS1P1, SHLD2P3, 51 more genes
nsv6620404	copy number variation	1	nstd224	human		GRCh37 chr10: 652,094-1,286,773 , GRCh38.p12 chr10: 606,154-1,244,721	ADARB2, WDR37, 12 more genes
nsv6622360	copy number variation	81	nstd224	human		GRCh37 chr14: 20,198,662-20,416,499 , GRCh38.p12 chr14: 19,730,503-19,948,340	OR4K6P, OR4K5, 11 more genes

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OSC7620 AND nstd224 (12)
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