1-0414-001 AND nstd173 - dbVar - NCBI

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4375278	copy number variation	38	nstd173	human		GRCh37 chr5: 104,433,421-104,498,053 , GRCh38.p12 chr5: 105,097,720-105,162,352	RAB9BP1
nsv4379109	copy number variation	1337	nstd173	human		GRCh37 chr20: 1,560,774-1,597,997 , GRCh38.p12 chr20: 1,580,128-1,617,351	SIRPB1
nsv4388396	copy number variation	1	nstd173	human		GRCh37 chr1: 241,194,662-241,215,273 , GRCh38.p12 chr1: 241,031,362-241,051,973	RGS7
nsv4388509	copy number variation	40	nstd173	human		GRCh37 chr6: 294,911-381,137 , GRCh38.p12 chr6: 294,911-381,137	DUSP22
nsv4366234	copy number variation	14	nstd173	human		GRCh37 chr7: 75,354,113-75,378,713 , GRCh38.p12 chr7: 75,724,795-75,749,395	HIP1
nsv4379956	copy number variation	132	nstd173	human		GRCh37 chr17: 44,212,824-44,292,754 , GRCh38.p12 chr17: 46,135,458-46,215,388 , GRCh38.p12 chr17\|NT_187663.1: 837,565-917,561	LOC107985027, KANSL1, 1 more genes
nsv4375232	copy number variation	423	nstd173	human		GRCh37 chr5: 180,375,302-180,430,801 , GRCh38.p12 chr5: 180,948,302-181,003,801	BTNL8, LOC100128762, 3 more genes
nsv4375922	copy number variation	10	nstd173	human		GRCh37 chrX: 103,261,175-103,305,297 , GRCh38.p12 chrX: 104,006,603-104,050,731	H2BW2, LOC107985662, 1 more genes
nsv4379920	copy number variation	11	nstd173	human		GRCh37 chr17: 36,243,781-36,404,555 , GRCh38.p12 chr17\|NT_187614.1: 2,122,846-2,283,620	NPEPPSP1, RNA5SP526, 8 more genes
nsv4375899	copy number variation	3	nstd173	human		GRCh37 chr7: 111,256,664-111,284,160 , GRCh38.p12 chr7: 111,616,608-111,644,104	0
nsv4376676	copy number variation	22	nstd173	human		GRCh37 chrX: 103,171,609-103,236,332 , GRCh38.p12 chrX: 103,917,015-103,981,754	SLC25A53P1, H2BW4P, 4 more genes
nsv4387972	copy number variation	19	nstd173	human		GRCh37 chr14: 22,533,752-22,974,280 , GRCh38.p12 chr14: 22,065,488-22,505,293	TRAV31, TRAJ58, 65 more genes
nsv4387178	copy number variation	6	nstd173	human		GRCh37 chr7: 38,293,950-38,395,208 , GRCh38.p12 chr7: 38,254,349-38,355,607	TRGV10, TRGVB, 19 more genes
nsv4373196	copy number variation	38	nstd173	human		GRCh37 chr6: 29,841,021-29,899,646 , GRCh38.p12 chr6: 29,873,244-29,931,869	DDX39BP1, HCG4P7, 8 more genes
nsv4373485	copy number variation	5	nstd173	human		GRCh37 chrX: 115,133,389-115,156,169 , GRCh38.p12 chr: NaN-NaN	0

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1-0414-001 AND nstd173 (16)
dbVar
Related DataSets for GEO Profiles (Select 28811800) (1)
GEO DataSets
Acute promyelocytic leukemia
Acute promyelocytic leukemia
Accession: GDS2242

GEO DataSets

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