SP56128 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
nsv909836	copy number variation	20	nstd71	human		NCBI36 chr18: 64,895,268-64,905,087 , GRCh37.p13 chr18: 66,744,288-66,754,107 , GRCh38.p12 chr18: 69,077,051-69,086,870	CCDC102B
nsv894543	copy number variation	1	nstd71	human		NCBI36 chr9: 138,991,966-138,994,558 , GRCh37.p13 chr9: 139,872,145-139,874,737 , GRCh38.p12 chr9: 136,977,693-136,980,285	PTGDS
nsv883266	copy number variation	1	nstd71	human		NCBI36 chr5: 178,848,390-178,869,328 , GRCh37.p13 chr5: 178,915,784-178,936,722 , GRCh38.p12 chr5: 179,488,783-179,509,721 , GRCh38.p12 chr5\|NW_016107298.1: 253,429-274,379	LOC100128622
nsv884355	copy number variation	4	nstd71	human		NCBI36 chr6: 31,467,172-31,505,856 , GRCh37.p13 chr6\|NT_167246.1: 2,705,640-2,742,426 , GRCh37.p13 chr6: 31,359,193-31,397,877 , GRCh37.p13 chr6\|NT_167249.1: 2,692,980-2,731,619 , GRCh38.p12 chr6\|NT_167249.2: 2,693,682-2,732,321 , GRCh38.p12 chr6: 31,391,416-31,430,100	MICA-AS1, MICA
nsv912241	copy number variation	1	nstd71	human		NCBI36 chr19: 53,891,727-53,901,038 , GRCh37.p13 chr19: 49,199,915-49,209,226 , GRCh38.p12 chr19: 48,696,658-48,705,969	FUT2, LOC105447645
nsv884391	copy number variation	1	nstd71	human		NCBI36 chr6: 31,510,107-31,561,526 , GRCh37.p13 chr6: 31,402,128-31,453,547 , GRCh38.p12 chr6: 31,434,351-31,485,770	MICB-DT, HCP5, 3 more genes
nsv904655	copy number variation	7	nstd71	human		NCBI36 chr16: 156,844-175,490 , GRCh37.p13 chr16: 216,844-235,490 , GRCh38.p12 chr16: 166,845-185,491	HBA2, HBM, 3 more genes
nsv883246	copy number variation	2	nstd71	human		NCBI36 chr5: 178,657,333-178,802,490 , GRCh37.p13 chr5: 178,724,727-178,869,884 , GRCh38.p12 chr5\|NW_016107298.1: 62,433-207,464 , GRCh38.p12 chr5: 179,297,726-179,442,883	LOC105377759, ADAMTS2, 1 more genes
nsv904048	copy number variation	34	nstd71	human		NCBI36 chr15: 32,509,924-32,606,592 , GRCh37.p13 chr15: 34,722,632-34,819,300 , GRCh38.p12 chr15: 34,430,431-34,527,099	DNM1P5, FSCN1P1, 4 more genes
nsv883824	copy number variation	3	nstd71	human		NCBI36 chr6: 29,978,470-30,004,400 , GRCh37.p13 chr6\|NT_167246.1: 1,164,662-1,190,626 , GRCh37.p13 chr6: 29,870,491-29,896,421 , GRCh38.p12 chr6\|NT_167246.2: 1,159,042-1,185,006 , GRCh38.p12 chr6: 29,902,714-29,928,644	HLA-K, HCG4B, 4 more genes
nsv903216	copy number variation	18	nstd71	human		NCBI36 chr15: 19,635,853-19,946,103 , GRCh37.p13 chr15: 21,371,194-22,444,739 , GRCh38.p12 chr15: 21,165,865-22,156,788	NF1P2, OR11J6P, 47 more genes
nsv872346	copy number variation	10	nstd71	human		NCBI36 chr1: 147,307,527-147,503,683 , GRCh37.p13 chr1: 149,040,903-149,237,059 , GRCh38.p12 chr1: 143,546,236-143,742,404	TRN-GTT6-1, PFN1P12, 10 more genes
nsv884849	copy number variation	16	nstd71	human		NCBI36 chr6: 32,561,832-32,576,147 , GRCh37.p13 chr6: 32,453,854-32,468,169 , GRCh38.p12 chr6: 32,486,077-32,500,392	0
nsv880294	copy number variation	63	nstd71	human		NCBI36 chr4: 162,075,534-162,151,909 , GRCh37.p13 chr4: 161,856,084-161,932,459 , GRCh38.p12 chr4: 160,934,932-161,011,307	0

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