MS20878 AND nstd71 - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv872693	copy number variation	223	nstd71	human		NCBI36 chr1: 187,587,641-187,815,034 , GRCh37.p13 chr1: 189,321,018-189,548,411 , GRCh38.p12 chr1: 189,351,888-189,579,281	LOC105371657
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
nsv889263	copy number variation	249	nstd71	human		NCBI36 chr7: 141,410,335-141,441,259 , GRCh37.p13 chr7\|NW_003571040.1: 206,017-236,941 , GRCh37.p13 chr7: 141,763,866-141,794,790 , GRCh38.p12 chr7: 142,064,066-142,094,990 , GRCh38.p12 chr7\|NT_187562.1: 25,946-56,870	MGAM
nsv914986	copy number variation	1	nstd71	human		NCBI36 chr22: 32,193,218-32,297,289 , GRCh37.p13 chr22: 33,863,218-33,967,289 , GRCh38.p12 chr22: 33,467,232-33,571,303	LARGE1
nsv914989	copy number variation	1	nstd71	human		NCBI36 chr22: 32,341,334-32,413,987 , GRCh37.p13 chr22: 34,011,334-34,083,987 , GRCh38.p12 chr22: 33,615,349-33,688,001	LARGE1
nsv908398	copy number variation	38	nstd71	human		NCBI36 chr17: 41,780,482-41,922,658 , GRCh37.p13 chr17: 44,424,726-44,566,775 , GRCh38.p12 chr17: 46,347,360-46,489,976	NSFP1, ARL17B
nsv914991	copy number variation	1	nstd71	human		NCBI36 chr22: 32,436,384-32,623,516 , GRCh37.p13 chr22: 34,106,384-34,293,516 , GRCh38.p12 chr22: 33,710,398-33,897,528	LARGE1, LARGE-AS1
nsv893187	copy number variation	5	nstd71	human		NCBI36 chr9: 43,520,820-43,641,682 , GRCh37.p13 chr9: 43,580,824-43,701,686 , GRCh38.p12 chr9: 42,112,703-42,233,565	CNTNAP3B, FAM74A7, 3 more genes
nsv912042	copy number variation	22	nstd71	human		NCBI36 chr19: 48,235,556-48,418,735 , GRCh37.p13 chr19: 43,543,716-43,726,895 , GRCh38.p12 chr19: 43,039,564-43,222,743	PSG2, LOC284344, 7 more genes
nsv906417	copy number variation	125	nstd71	human		NCBI36 chr16: 32,469,358-32,511,911 , GRCh37.p13 chr16: 32,561,857-32,604,410 , GRCh38.p12 chr16: 32,550,536-32,593,089	0
nsv905930	copy number variation	6	nstd71	human		NCBI36 chr16: 32,406,646-32,424,534 , GRCh37.p13 chr16: 32,499,145-32,517,033 , GRCh38.p12 chr16: 32,487,824-32,505,712	0
nsv906198	copy number variation	3	nstd71	human		NCBI36 chr16: 32,439,163-32,454,604 , GRCh37.p13 chr16: 32,531,662-32,547,103 , GRCh38.p12 chr16: 32,520,341-32,535,782	0
nsv883886	copy number variation	3	nstd71	human		NCBI36 chr6: 29,983,504-30,004,400 , GRCh37.p13 chr6\|NT_167246.1: 1,169,702-1,190,626 , GRCh37.p13 chr6: 29,875,525-29,896,421 , GRCh38.p12 chr6: 29,907,748-29,928,644 , GRCh38.p12 chr6\|NT_167246.2: 1,164,082-1,185,006	HCG4B, LOC353008, 4 more genes
nsv901296	copy number variation	150	nstd71	human		NCBI36 chr14: 19,261,709-19,494,891 , GRCh37.p13 chr14: 20,191,869-20,425,051 , GRCh38.p12 chr14: 19,723,710-19,956,892	OR4K16P, OR4K2, 12 more genes

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