14-0024-002 AND nstd173 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv4368029	copy number variation	55	nstd173	human	GRCh37 chr10: 68,077,579-68,122,519 , GRCh38.p12 chr10: 66,317,821-66,362,761	CTNNA3
nsv4379349	copy number variation	357	nstd173	human	GRCh37 chr20: 1,560,549-1,597,997 , GRCh38.p12 chr20: 1,579,903-1,617,351	SIRPB1
nsv4380512	copy number variation	13	nstd173	human	GRCh37 chr3: 89,386,935-89,419,375 , GRCh38.p12 chr3: 89,337,785-89,370,225	EPHA3
nsv4388221	copy number variation	6	nstd173	human	GRCh37 chr3: 84,844,800-84,873,060 , GRCh38.p12 chr3: 84,795,649-84,823,909 , GRCh38.p12 chr3\|NW_018654711.1: 1-23,942	LINC00971
nsv4365093	copy number variation	508	nstd173	human	GRCh37 chr13: 57,758,269-57,778,379 , GRCh38.p12 chr13: 57,184,135-57,204,245	MTCO2P3
nsv4382544	copy number variation	91	nstd173	human	GRCh37 chr2: 98,138,405-98,162,176 , GRCh38.p12 chr2: 97,521,942-97,545,713	ANKRD36B
nsv4371805	copy number variation	282	nstd173	human	GRCh37 chr11: 18,941,197-18,961,975 , GRCh38.p12 chr11: 18,919,650-18,940,428	MRGPRX1
nsv4367066	copy number variation	60	nstd173	human	GRCh37 chr14: 86,460,915-86,494,554 , GRCh38.p12 chr14: 85,994,571-86,028,210	LINC02316, LINC02328
nsv4385636	copy number variation	51	nstd173	human	GRCh37 chr2: 13,202,931-13,279,945 , GRCh38.p12 chr2: 13,062,806-13,139,820	LOC105373436, LOC105373484
nsv4384457	copy number variation	635	nstd173	human	GRCh37 chr11: 55,374,031-55,453,008 , GRCh38.p12 chr11: 55,606,555-55,685,532	OR4P1P, OR4C6, 3 more genes
nsv4378623	copy number variation	41	nstd173	human	GRCh37 chr6: 254,254-294,923 , GRCh38.p12 chr6: 254,254-294,923	, DUSP22, 1 more genes
nsv4381596	copy number variation	144	nstd173	human	GRCh37 chr14: 74,001,123-74,024,031 , GRCh38.p12 chr14: 73,534,419-73,557,327	HEATR4, NT5CP2, 1 more genes
nsv4366126	copy number variation	1	nstd173	human	GRCh37 chr2: 198,145,545-198,236,716 , GRCh38.p12 chr2: 197,280,821-197,371,992	ANKRD44, ANKRD44-IT1, 1 more genes
nsv4388097	copy number variation	2	nstd173	human	GRCh37 chr1: 1,627,906-1,675,073 , GRCh38.p12 chr1: 1,696,467-1,743,634	MMP23A, LOC100129381, 2 more genes
nsv4380515	copy number variation	77	nstd173	human	GRCh37 chr12: 8,558,475-8,594,982 , GRCh38.p12 chr12: 8,405,879-8,442,386	OR7E148P, OR7E149P, 1 more genes
nsv4375644	copy number variation	145	nstd173	human	GRCh37 chr22: 25,656,238-25,922,334 , GRCh38.p12 chr22: 25,260,271-25,526,367	CRYBB2P1, IGLL3P, 4 more genes
nsv4374200	copy number variation	1	nstd173	human	GRCh37 chr1: 206,313,488-206,539,650 , GRCh38.p12 chr: NaN-NaN	0
nsv4387150	copy number variation	27	nstd173	human	GRCh37 chr19: 24,378,991-24,419,660 , GRCh38.p12 chr19: 24,196,189-24,236,858	0
nsv4374519	copy number variation	45	nstd173	human	GRCh37 chr13: 69,238,142-69,264,684 , GRCh38.p12 chr13: 68,664,010-68,690,552	0
nsv4386306	copy number variation	141	nstd173	human	GRCh37 chrX: 924,088-944,608 , GRCh38.p12 chrX: 963,353-983,873	0

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 28

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Number of Variants: 20

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