OSC6622 AND nstd224 - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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
nsv6625091	copy number variation	291	nstd224	human		GRCh37 chr1: 110,228,505-110,241,385 , GRCh38.p12 chr1: 109,685,883-109,698,763	GSTM1
nsv6623269	copy number variation	1	nstd224	human		GRCh37 chr15: 52,998,842-53,037,849 , GRCh38.p12 chr15: 52,706,645-52,745,652	ATOSA
nsv6629501	copy number variation	16	nstd224	human		GRCh37 chr4: 58,056,308-58,088,414 , GRCh38.p12 chr4: 57,190,142-57,222,248	IGFBP7-AS1
nsv6624041	copy number variation	1	nstd224	human		GRCh37 chr17: 1,268,683-1,333,949 , GRCh38.p12 chr17: 1,365,389-1,430,655 , GRCh38.p12 chr17\|NT_187613.1: 307,415-372,681	CRK, YWHAE
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
nsv6626369	copy number variation	153	nstd224	human		GRCh37 chr1: 25,604,951-25,655,563 , GRCh38.p12 chr1: 25,278,460-25,329,072	RSRP1, RHD, 1 more genes
nsv6620825	copy number variation	1	nstd224	human		GRCh37 chr11: 134,854,531-134,903,770 , GRCh38.p12 chr11: 134,984,637-135,033,876	LINC02717, LOC100507548, 1 more genes
nsv6628364	copy number variation	27	nstd224	human		GRCh37 chr2: 89,504,808-90,241,820 , GRCh38.p12 chr2: 89,205,323-90,202,954	IGKV6D-41, IGKV3D-31, 52 more genes
nsv6629162	copy number variation	1	nstd224	human		GRCh37 chr4: 137,436,396-137,477,377 , GRCh38.p12 chr4: 136,515,241-136,556,222	0
nsv6631082	copy number variation	194	nstd224	human		GRCh37 chr6: 67,017,494-67,044,618 , GRCh38.p12 chr6: 66,307,601-66,334,725	0
nsv6627783	copy number variation	20	nstd224	human		GRCh37 chr2: 17,220,772-17,239,045 , GRCh38.p12 chr2: 17,039,505-17,057,778	0

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OSC6622 AND nstd224 (13)
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