MS21928 AND nstd71 - 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
nsv897250	copy number variation	18	nstd71	human		NCBI36 chr11: 38,205,782-38,296,860 , GRCh37.p13 chr11: 38,249,206-38,340,284 , GRCh38.p12 chr11: 38,227,656-38,318,734	LOC105376634
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
nsv888917	copy number variation	11	nstd71	human		NCBI36 chr7: 102,041,825-102,062,128 , GRCh37.p13 chr7: 102,254,605-102,274,889 , GRCh38.p12 chr7: 102,614,158-102,634,442	RASA4
nsv883993	copy number variation	42	nstd71	human		NCBI36 chr6: 30,032,109-30,045,903 , GRCh37.p13 chr6\|NT_167246.1: 1,222,754-1,236,501 , GRCh37.p13 chr6\|NT_167247.1: 1,306,026-1,319,775 , GRCh37.p13 chr6: 29,924,130-29,937,924 , GRCh38.p12 chr6\|NT_167246.2: 1,217,134-1,230,881 , GRCh38.p12 chr6\|NT_167247.2: 1,300,441-1,314,190 , GRCh38.p12 chr6: 29,956,353-29,970,147	HLA-W, MICD
nsv883869	copy number variation	6	nstd71	human		NCBI36 chr6: 29,982,594-29,992,880 , GRCh37.p13 chr6\|NT_167246.1: 1,168,792-1,179,076 , GRCh37.p13 chr6: 29,874,615-29,884,901 , GRCh38.p12 chr6\|NT_167246.2: 1,163,172-1,173,456 , GRCh38.p12 chr6: 29,906,838-29,917,124	DDX39BP1, MCCD1P1, 2 more genes
nsv904023	copy number variation	257	nstd71	human		NCBI36 chr15: 32,487,589-32,625,184 , GRCh37.p13 chr15: 34,700,297-34,837,892 , GRCh38.p12 chr15: 34,408,096-34,545,691	LOC100422491, GOLGA8B, 5 more genes
nsv886057	copy number variation	200	nstd71	human		NCBI36 chr6: 67,065,007-67,111,682 , GRCh37.p13 chr6: 67,008,286-67,054,961 , GRCh38.p12 chr6: 66,298,393-66,345,068	0
nsv883609	copy number variation	2	nstd71	human		NCBI36 chr6: 29,961,934-29,982,364 , GRCh37.p13 chr6\|NT_167246.1: 1,157,859-1,168,562 , GRCh37.p13 chr6: 29,853,955-29,874,385 , GRCh38.p12 chr6\|NT_167246.2: 1,152,239-1,162,942 , GRCh38.p12 chr6: 29,886,178-29,906,608	HLA-H, HCG4P7, 4 more genes
nsv906262	copy number variation	4	nstd71	human		NCBI36 chr16: 32,441,070-32,511,911 , GRCh37.p13 chr16: 32,533,569-32,604,410 , GRCh38.p12 chr16: 32,522,248-32,593,089	0

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MS21928 AND nstd71 (10)
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