OSC8854 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
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
nsv6629011	copy number variation	1	nstd224	human		GRCh37 chr3: 33,214,676-33,228,903 , GRCh38.p12 chr3: 33,173,184-33,187,411	SUSD5
nsv6623453	copy number variation	9	nstd224	human		GRCh37 chr16: 32,509,483-32,612,821 , GRCh38.p12 chr16: 32,498,162-32,601,500	FAM153DP
nsv6628756	copy number variation	1	nstd224	human		GRCh37 chr3: 25,106,437-25,146,328 , GRCh38.p12 chr3: 25,064,946-25,104,837	RARB
nsv6631536	copy number variation	1	nstd224	human		GRCh37 chr6: 7,427,500-7,454,812 , GRCh38.p12 chr6: 7,427,267-7,454,579	LOC102724234
nsv6632549	copy number variation	6	nstd224	human		GRCh37 chr8: 2,537,640-2,552,691 , GRCh38.p12 chr8: 2,680,144-2,695,189 , GRCh38.p12 chr8\|NT_187576.1: 848,210-863,255	LINC03021
nsv6622494	copy number variation	1	nstd224	human		GRCh37 chr14: 21,404,727-21,428,496 , GRCh38.p12 chr14: 20,936,568-20,960,337	LOC100507513, RNASE2
nsv6627379	copy number variation	4	nstd224	human		GRCh37 chr22: 24,374,253-24,386,042 , GRCh38.p12 chr22\|NT_187633.1: 268,428-280,217	GSTT1-AS1, GSTTP2, 2 more genes
nsv6625857	copy number variation	2	nstd224	human		GRCh37 chr1: 161,500,105-161,522,542 , GRCh38.p12 chr1: 161,530,315-161,552,752	TRG-TCC2-6, TRN-GTT1-1, 3 more genes
nsv6629111	copy number variation	18	nstd224	human		GRCh37 chr4: 138,180,226-138,191,422 , GRCh38.p12 chr4: 137,259,072-137,270,268	0
nsv6620628	copy number variation	93	nstd224	human		GRCh37 chr10: 47,146,867-47,703,869 , GRCh38.p12 chr10: 46,157,935-47,739,149	GDF10, RBP3, 48 more genes

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OSC8854 AND nstd224 (12)
dbVar

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