OSC8804 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
nsv6630339	copy number variation	71	nstd224	human		GRCh37 chr5: 32,120,277-32,160,019 , GRCh38.p12 chr5: 32,120,171-32,159,913	GOLPH3
nsv6625543	copy number variation	4	nstd224	human		GRCh37 chr1: 110,230,206-110,253,911 , GRCh38.p12 chr1: 109,687,584-109,711,289	GSTM5, GSTM1
nsv6631158	copy number variation	3	nstd224	human		GRCh37 chr6: 31,360,255-31,377,047 , GRCh38.p12 chr6: 31,392,478-31,409,270	MICA-AS1, MICA
nsv6631484	copy number variation	1	nstd224	human		GRCh37 chr6: 31,456,567-31,475,513 , GRCh38.p12 chr6: 31,488,790-31,507,736	MICB, MICB-DT
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
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
nsv6627380	copy number variation	480	nstd224	human		GRCh37 chr22: 24,374,253-24,390,432 , GRCh38.p12 chr22\|NT_187633.1: 268,428-284,607	GSTTP2, GSTT1-AS1, 2 more genes
nsv6626736	copy number variation	3	nstd224	human		GRCh37 chr21: 14,595,742-15,263,760 , GRCh38.p12 chr21: 13,223,421-13,891,439	CYP4F29P, POTED, 24 more genes
nsv6621659	copy number variation	3	nstd224	human		GRCh37 chr13: 19,280,540-19,436,438 , GRCh38.p12 chr13: 18,706,400-18,850,544 , GRCh38.p12 chr13\|NT_187594.1: 8,050-152,194	SNX18P26, RHOT1P3, 8 more genes
nsv6624284	copy number variation	18	nstd224	human		GRCh37 chr17: 44,229,787-44,353,222 , GRCh38.p12 chr17: 46,152,421-46,275,856 , GRCh38.p12 chr17\|NT_187663.1: 854,525-954,783	KANSL1, KANSL1-AS1, 5 more genes
nsv6627895	copy number variation	12	nstd224	human		GRCh37 chr2: 57,402,202-57,455,549 , GRCh38.p12 chr2: 57,175,067-57,228,414	0

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