MS16821 AND nstd71 - 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
nsv892926	copy number variation	1	nstd71	human		NCBI36 chr9: 29,547,353-29,595,173 , GRCh37.p13 chr9: 29,557,353-29,605,173 , GRCh38.p12 chr9: 29,557,355-29,605,175	LOC105376005
nsv884822	copy number variation	2547	nstd71	human		NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715	HLA-DRB5
nsv911749	copy number variation	35	nstd71	human		NCBI36 chr19: 46,044,103-46,075,668 , GRCh37.p13 chr19: 41,352,263-41,383,828 , GRCh38.p12 chr19: 40,846,358-40,877,923	CYP2A6, CYP2A7
nsv908504	copy number variation	1	nstd71	human		NCBI36 chr17: 41,841,908-41,943,845 , GRCh37.p13 chr17: 44,486,492-44,588,529 , GRCh38.p12 chr17: 46,444,391-46,511,163	ARL17A, LRRC37A2
nsv883598	copy number variation	4	nstd71	human		NCBI36 chr6: 29,959,422-29,980,430 , GRCh37.p13 chr6: 29,851,443-29,872,451 , GRCh38.p12 chr6: 29,883,666-29,904,674	DDX39BP1, HLA-T, 2 more genes
nsv892113	copy number variation	1	nstd71	human		NCBI36 chr9: 4,311,558-4,373,319 , GRCh37.p13 chr9: 4,321,558-4,383,319 , GRCh38.p12 chr9: 4,321,558-4,383,319	0
nsv890133	copy number variation	6	nstd71	human		NCBI36 chr8: 7,200,170-7,459,302 , GRCh37.p13 chr8: 7,212,760-7,471,892 , GRCh38.p12 chr8\|NT_187570.1: 78,282-297,473 , GRCh38.p12 chr8: 7,355,238-7,614,370	FAM90A6P, LOC105377801, 20 more genes
nsv901294	copy number variation	38	nstd71	human		NCBI36 chr14: 19,261,709-19,493,705 , GRCh37.p13 chr14: 20,191,869-20,423,865 , GRCh38.p12 chr14: 19,723,710-19,955,706	OR4K5, OR4Q3, 12 more genes
nsv890310	copy number variation	1	nstd71	human		NCBI36 chr8: 7,731,195-7,908,368 , GRCh37.p13 chr8: 7,693,785-7,870,958 , GRCh38.p12 chr8: 7,836,263-8,013,436	DEFB109C, SPAG11A, 11 more genes
nsv896324	copy number variation	16	nstd71	human		NCBI36 chr10: 135,075,656-135,252,190 , GRCh37.p13 chr10: 135,225,666-135,402,200 , GRCh38.p12 chr10: 133,412,162-133,588,696	SPRN, SPRNP1, 10 more genes
nsv906641	copy number variation	6	nstd71	human		NCBI36 chr16: 33,786,957-33,819,975 , GRCh37.p13 chr16: 33,879,456-33,912,474 , GRCh38.p12 chr16: 34,076,989-34,110,007	0

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