MS22848 AND nstd71 - dbVar - NCBI

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Number of Variants: 8

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv890816	copy number variation	21	nstd71	human		NCBI36 chr8: 39,421,344-39,497,557 , GRCh37.p13 chr8: 39,302,187-39,378,400 , GRCh38.p12 chr8: 39,444,668-39,520,881	ADAM3A
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
nsv893661	copy number variation	1	nstd71	human		NCBI36 chr9: 104,982,210-105,116,091 , GRCh37.p13 chr9: 105,942,389-106,076,270 , GRCh38.p12 chr9: 103,180,107-103,313,988	LINC01492
nsv908379	copy number variation	346	nstd71	human		NCBI36 chr17: 41,775,690-41,922,658 , GRCh37.p13 chr17: 44,419,932-44,566,775 , GRCh38.p12 chr17: 46,342,566-46,489,976	ARL17B, NSFP1, 1 more genes
nsv885535	copy number variation	7	nstd71	human		NCBI36 chr6: 32,708,781-32,728,261 , GRCh37.p13 chr6\|NT_167247.1: 3,939,666-3,952,277 , GRCh37.p13 chr6\|NT_167245.1: 3,882,525-3,895,103 , GRCh37.p13 chr6\|NT_167249.1: 4,034,248-4,046,862 , GRCh37.p13 chr6\|NT_167246.1: 4,056,958-4,069,536 , GRCh37.p13 chr6: 32,600,803-32,620,283 , GRCh38.p12 chr6\|NT_167245.2: 3,876,940-3,889,518 , GRCh38.p12 chr6: 32,633,026-32,652,506 , GRCh38.p12 chr6\|NT_167249.2: 4,034,950-4,047,564 , GRCh38.p12 chr6\|NT_167246.2: 4,051,338-4,063,916 , GRCh38.p12 chr6\|NT_167247.2: 3,934,081-3,946,695	HLA-DQA1, , 2 more genes
nsv875077	copy number variation	4	nstd71	human		NCBI36 chr2: 130,602,361-130,851,319 , GRCh37.p13 chr2: 130,885,891-131,134,849 , GRCh38.p12 chr2: 130,128,318-130,377,276	MTND3P15, MTCO2P7, 25 more genes
nsv906245	copy number variation	9	nstd71	human		NCBI36 chr16: 32,439,877-32,511,911 , GRCh37.p13 chr16: 32,532,376-32,604,410 , GRCh38.p12 chr16: 32,521,055-32,593,089	0
nsv901912	copy number variation	19	nstd71	human		NCBI36 chr14: 47,529,415-47,549,498 , GRCh37.p13 chr14: 48,459,665-48,479,748 , GRCh38.p12 chr14: 47,990,462-48,010,545	0

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