OSC8189 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
nsv6629427	copy number variation	35	nstd224	human		GRCh37 chr4: 25,557,474-25,578,529 , GRCh38.p12 chr4: 25,555,852-25,576,907	LOC101929161
nsv6630433	copy number variation	28	nstd224	human		GRCh37 chr5: 700,560-785,864 , GRCh38.p12 chr5: 700,445-785,749	ZDHHC11B, TPPP
nsv6624685	copy number variation	256	nstd224	human		GRCh37 chr19: 20,605,360-20,700,135 , GRCh38.p12 chr19: 20,422,554-20,517,329	BNIP3P23, LOC105372317, 2 more genes
nsv6624626	copy number variation	1	nstd224	human		GRCh37 chr18: 92,127-312,221 , GRCh38.p12 chr18: 92,127-312,221	USP14, THOC1, 3 more genes
nsv6634194	copy number variation	1	nstd224	human		GRCh37 chrX: 122,602,599-122,729,614 , GRCh38.p12 chrX: 123,468,748-123,595,763	GRIA3, TUBB4AP1, 2 more genes
nsv6621101	copy number variation	1	nstd224	human		GRCh37 chr11: 48,416,898-48,925,223 , GRCh38.p12 chr11: 48,395,346-48,903,671	OR4C10P, OR4A40P, 12 more genes
nsv6626850	copy number variation	52	nstd224	human		GRCh37 chr21: 15,248,281-15,258,717 , GRCh38.p12 chr21: 13,875,960-13,886,396	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
nsv6622620	copy number variation	10	nstd224	human		GRCh37 chr15: 22,759,530-23,279,684 , GRCh38.p12 chr15: 22,593,412-23,113,538	TUBGCP5, ELMO2P1, 13 more genes
nsv6623614	copy number variation	36	nstd224	human		GRCh37 chr16: 34,489,371-34,740,580 , GRCh38.p12 chr16: 35,255,000-35,506,209	LINC01566, AGGF1P9, 23 more genes
nsv6620284	copy number variation	1	nstd224	human		GRCh37 chr10: 20,783,713-20,806,108 , GRCh38.p12 chr10: 20,494,784-20,517,179	0

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