MS11084 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
nsv909839	copy number variation	966	nstd71	human		NCBI36 chr18: 64,895,268-64,909,808 , GRCh37.p13 chr18: 66,744,288-66,758,828 , GRCh38.p12 chr18: 69,077,051-69,091,591	CCDC102B
nsv905609	copy number variation	2	nstd71	human		NCBI36 chr16: 22,521,490-22,610,270 , GRCh37.p13 chr16: 22,613,989-22,702,769 , GRCh38.p12 chr16: 22,602,668-22,691,448	LOC112268175
nsv904034	copy number variation	25	nstd71	human		NCBI36 chr15: 32,506,097-32,569,800 , GRCh37.p13 chr15: 34,718,805-34,782,508 , GRCh38.p12 chr15: 34,426,604-34,490,307	HNRNPLP2, GOLGA8A
nsv879318	copy number variation	371	nstd71	human		NCBI36 chr4: 69,085,989-69,179,871 , GRCh37.p13 chr4: 69,403,394-69,497,276 , GRCh38.p12 chr4: 68,537,676-68,631,558	LOC728807, UGT2B17, 2 more genes
nsv893341	copy number variation	2	nstd71	human		NCBI36 chr9: 45,763,238-45,888,287 , GRCh37.p13 chr9: 45,873,242-45,998,291 , GRCh38.p12 chr9: 41,403,975-41,483,020	RPL7AP45, , 2 more genes
nsv871196	copy number variation	88	nstd71	human		NCBI36 chr1: 12,777,429-12,810,136 , GRCh37.p13 chr1: 12,854,842-12,887,549 , GRCh38.p12 chr1: 12,794,693-12,827,690	PRAMEF11, PRAMEF1, 1 more genes
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
nsv871828	copy number variation	1	nstd71	human		NCBI36 chr1: 64,134,548-64,275,183 , GRCh37.p13 chr1: 64,361,960-64,502,595 , GRCh38.p12 chr1: 63,896,289-64,036,923	RNU6-809P, LOC105378772, 1 more genes
nsv882048	copy number variation	14	nstd71	human		NCBI36 chr5: 70,183,438-70,300,876 , GRCh37.p13 chr5: 70,147,682-70,265,120 , GRCh38.p12 chr5: 70,851,855-70,969,293	GUSBP16, LOC107986373, 4 more genes
nsv881870	copy number variation	38	nstd71	human		NCBI36 chr5: 69,319,133-69,436,209 , GRCh37.p13 chr5: 69,283,377-69,400,453 , GRCh38.p12 chr5\|NT_187651.1: 243,313-329,959 , GRCh38.p12 chr5: 69,987,550-70,104,626	SMN2, LOC105369228, 5 more genes
nsv883590	copy number variation	89	nstd71	human		NCBI36 chr6: 29,957,666-30,004,400 , GRCh37.p13 chr6: 29,849,687-29,896,421 , GRCh37.p13 chr6\|NT_167246.1: 1,157,859-1,190,626 , GRCh38.p12 chr6: 29,881,910-29,928,644 , GRCh38.p12 chr6\|NT_167246.2: 1,152,239-1,185,006	MCCD1P1, HLA-H, 7 more genes
nsv905991	copy number variation	55	nstd71	human		NCBI36 chr16: 32,410,369-32,511,911 , GRCh37.p13 chr16: 32,502,868-32,604,410 , GRCh38.p12 chr16: 32,491,547-32,593,089	0
nsv886198	copy number variation	304	nstd71	human		NCBI36 chr6: 77,073,066-77,088,077 , GRCh37.p13 chr6: 77,016,346-77,031,357 , GRCh38.p12 chr6: 76,306,629-76,321,640	0
nsv884228	copy number variation	228	nstd71	human		NCBI36 chr6: 31,385,967-31,398,785 , GRCh37.p13 chr6\|NT_167249.1: 2,611,726-2,624,528 , GRCh37.p13 chr6\|NT_167246.1: 2,624,814-2,631,393 , GRCh37.p13 chr6: 31,277,988-31,290,806 , GRCh38.p12 chr6: 31,310,211-31,323,029 , GRCh38.p12 chr6\|NT_167246.2: 2,619,194-2,625,775 , GRCh38.p12 chr6\|NT_167249.2: 2,612,428-2,625,230	0

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