59962L AND nstd12 - dbVar - NCBI

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Items: 9

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv432290	copy number variation	1	nstd12	human		NCBI35 chrX: 25,516,263-25,620,400 , GRCh37.p13 chrX: 25,756,606-25,860,743 , GRCh38.p12 chrX: 25,738,489-25,842,626	LOC107985707
nsv432719	copy number variation	5	nstd12	human		NCBI35 chr5: 15,772,222-15,773,478 , GRCh37.p13 chr5: 15,719,222-15,720,478 , GRCh38.p12 chr5: 15,719,113-15,720,369	FBXL7
nsv430269	copy number variation	1	nstd12	human		NCBI35 chr1: 204,784,551-204,848,000 , GRCh37.p13 chr1: 208,396,156-208,459,605 , GRCh38.p12 chr1: 208,222,811-208,286,260	PLXNA2, LOC105372884, 2 more genes
nsv429778	copy number variation	2	nstd12	human		NCBI35 chr7: 75,781,935-76,210,401 , GRCh37.p13 chr7: 76,137,284-76,565,750 , GRCh38.p12 chr7: 76,507,967-76,936,433	POMZP3, LINC03009, 6 more genes
nsv432359	copy number variation	1	nstd12	human		NCBI35 chrX: 130,406,000-130,695,499 , GRCh37.p13 chrX: 130,680,465-130,969,964 , GRCh38.p12 chrX: 131,546,491-131,835,936	OR2AF1P, OR7L1P, 5 more genes
nsv430167	copy number variation	5	nstd12	human		NCBI35 chr10: 46,363,383-47,485,200 , GRCh37.p13 chr10\|NW_003871068.1: 431,049-2,010,264 , GRCh37.p13 chr10: 47,006,954-47,965,194 , GRCh38.p12 chr10: 46,157,935-47,923,579	CTSLP2, GDF2, 54 more genes
nsv430970	copy number variation	1	nstd12	human		NCBI35 chr14: 21,632,122-22,008,401 , GRCh37.p13 chr14: 22,562,282-22,938,561 , GRCh38.p12 chr14: 22,094,005-22,469,569	TRA, TRD, 36 more genes
nsv430284	copy number variation	2	nstd12	human		NCBI35 chr10: 135,079,239-135,323,432 , GRCh37.p13 chr10: 135,190,358-135,434,551 , GRCh38.p12 chr10: 133,376,854-133,621,047	CYP2E1, OR7M1P, 11 more genes
nsv431277	complex substitution	1	nstd12	human		NCBI35 chr15: 18,682,601-20,089,383 , GRCh37.p13 chr15: 20,422,587-22,588,019 , GRCh38.p12 chr15: 20,217,334-22,300,068	NBEAP1, OR4H6P, 89 more genes

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