sample84 AND nstd145 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv3113301	copy number variation	16	nstd145	human	GRCh37 chr1: 189,326,143-189,543,860 , GRCh38.p12 chr1: 189,357,013-189,574,730	LOC105371657
nsv3118081	copy number variation	72	nstd145	human	GRCh37 chr7: 141,766,533-141,793,377 , GRCh38.p12 chr7\|NT_187562.1: 28,613-55,457 , GRCh38.p12 chr7: 142,066,733-142,093,577	MGAM
nsv3117809	copy number variation	152	nstd145	human	GRCh37 chr20: 1,561,593-1,584,273 , GRCh38.p12 chr20: 1,580,947-1,603,627	SIRPB1
nsv3116648	copy number variation	8	nstd145	human	GRCh37 chrY: 24,872,998-24,885,872 , GRCh38.p12 chrY: 22,726,851-22,739,725	FAM8A10P
nsv3112094	copy number variation	94	nstd145	human	GRCh37 chr7: 133,785,285-133,797,218 , GRCh38.p12 chr7: 134,100,532-134,112,465
nsv3110986	copy number variation	37	nstd145	human	GRCh37 chr5: 17,640,200-17,651,341 , GRCh38.p12 chr5: 17,640,091-17,651,232	LOC391768
nsv3113383	copy number variation	199	nstd145	human	GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219	VEZF1P1
nsv3110942	copy number variation	60	nstd145	human	GRCh37 chr7: 91,033,585-91,042,496 , GRCh38.p12 chr7: 91,404,270-91,413,181	LINC02932
nsv3117545	copy number variation	9	nstd145	human	GRCh37 chrX: 29,600,070-29,608,901 , GRCh38.p12 chrX: 29,581,953-29,590,784	IL1RAPL1
nsv3114475	copy number variation	50	nstd145	human	GRCh37 chr5: 12,811,448-12,818,768 , GRCh38.p12 chr5: 12,811,336-12,818,656	LOC105374657
nsv3116197	copy number variation	63	nstd145	human	GRCh37 chr7: 151,606-157,474 , GRCh38.p12 chr7: 151,606-157,474 , GRCh38.p12 chr7\|NT_187558.1: 107,411-113,280 , GRCh38.p12 chr7\|NT_187653.1: 143,927-149,795	LINC03014
nsv3115596	copy number variation	45	nstd145	human	GRCh37 chr3: 148,964,056-148,969,130 , GRCh38.p12 chr3: 149,246,269-149,251,343	CPHL1P
nsv3110559	copy number variation	79	nstd145	human	GRCh37 chr2: 49,534,030-49,539,079 , GRCh38.p12 chr2: 49,306,891-49,311,940	LOC105374595
nsv3117774	copy number variation	53	nstd145	human	GRCh37 chr1: 174,796,674-174,801,029 , GRCh38.p12 chr1: 174,827,536-174,831,891	RABGAP1L
nsv3113346	copy number variation	33	nstd145	human	GRCh37 chr9: 29,093,646-29,097,821 , GRCh38.p12 chr9: 29,093,648-29,097,823	LINGO2
nsv3110679	copy number variation	7	nstd145	human	GRCh37 chr7: 78,130,707-78,134,821 , GRCh38.p12 chr7: 78,501,390-78,505,504	MAGI2
nsv3117571	copy number variation	81	nstd145	human	GRCh37 chr11: 107,239,191-107,242,941 , GRCh38.p12 chr11: 107,368,465-107,372,215	CWF19L2
nsv3114451	copy number variation	90	nstd145	human	GRCh37 chr12: 90,487,994-90,491,654 , GRCh38.p12 chr12: 90,094,217-90,097,877	LOC105369890
nsv3113027	copy number variation	2	nstd145	human	GRCh37 chrX: 148,711,463-148,715,026 , GRCh38.p12 chrX: 149,629,782-149,633,370	TMEM185A
nsv3114666	copy number variation	1	nstd145	human	GRCh37 chr4: 62,615,746-62,619,298 , GRCh38.p12 chr4: 61,750,028-61,753,580	ADGRL3

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 76

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Number of Variants: 20

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