1-0864-003 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
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
nsv4368760	copy number variation	4	nstd173	human	GRCh37 chr12: 11,503,224-11,560,919 , GRCh38.p12 chr12: 11,350,290-11,407,985	PRB1, PRB2
nsv4387593	copy number variation	3	nstd173	human	GRCh37 chr10: 96,497,261-96,546,547 , GRCh38.p12 chr10: 94,737,504-94,786,790	MTND4P19, CYP2C19
nsv4382990	copy number variation	15	nstd173	human	GRCh37 chr9: 115,854,353-115,881,587 , GRCh38.p12 chr9: 113,092,073-113,119,307	FAM225B, FAM225A
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
nsv4387832	copy number variation	38	nstd173	human	GRCh37 chr12: 11,216,817-11,256,413 , GRCh38.p12 chr12: 11,064,218-11,103,814	TAS2R43, PRH1-TAS2R14, 3 more genes
nsv4377999	copy number variation	1	nstd173	human	GRCh37 chrX: 95,057,196-95,349,212 , GRCh38.p12 chrX: 95,802,197-96,094,213	RN7SL379P, KAT7P1, 1 more genes
nsv4376452	copy number variation	337	nstd173	human	GRCh37 chr17: 34,437,494-34,477,480 , GRCh38.p12 chr17: 36,110,101-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 64,198-104,195 , GRCh38.p12 chr17\|NT_187614.1: 345,022-385,008	LOC101927369, LOC107985055, 3 more genes
nsv4370380	copy number variation	1	nstd173	human	GRCh37 chr11: 55,403,432-55,442,305 , GRCh38.p12 chr11: 55,635,956-55,674,829	OR4S2, OR4V1P, 2 more genes
nsv4379112	copy number variation	1	nstd173	human	GRCh37 chrX: 134,848,794-134,891,198 , GRCh38.p12 chrX: 135,760,480-135,798,648	CT45A5, CT45A3, 1 more genes
nsv4371902	copy number variation	41	nstd173	human	GRCh37 chr6: 67,004,973-67,048,629 , GRCh38.p12 chr6: 66,295,080-66,338,736	0
nsv4377642	copy number variation	2	nstd173	human	GRCh37 chr2: 34,701,643-34,737,931 , GRCh38.p12 chr2: 34,476,576-34,512,864	0
nsv4380160	copy number variation	62	nstd173	human	GRCh37 chr6: 110,394,605-110,415,415 , GRCh38.p12 chr6: 110,073,402-110,094,212	0
nsv4368871	copy number variation	21	nstd173	human	GRCh37 chr10: 46,966,534-47,149,423 , GRCh38.p12 chr10: 46,400,340-46,583,083	GPRIN2, , 5 more genes
nsv4370895	copy number variation	1	nstd173	human	GRCh37 chrX: 134,947,464-134,969,327 , GRCh38.p12 chrX: 135,800,582-135,886,767	CT45A2, CT45A9, 4 more genes
nsv4369404	copy number variation	213	nstd173	human	GRCh37 chr14: 107,150,444-107,179,594 , GRCh38.p12 chr14: 106,694,427-106,771,352	IGHV2-70, IGH, 7 more genes
nsv4380168	copy number variation	295	nstd173	human	GRCh37 chr17: 44,187,492-44,784,639 , GRCh38.p12 chr17: 46,110,126-46,707,273 , GRCh38.p12 chr17\|NT_187663.1: 812,225-1,226,699	MAPK8IP1P1, DND1P2, 14 more genes
nsv4386370	copy number variation	1	nstd173	human	GRCh37 chr14: 22,626,948-22,959,540 , GRCh38.p12 chr14: 22,159,015-22,490,552	TRAJ60, TRAV33, 43 more genes
nsv4370946	copy number variation	301	nstd173	human	GRCh37 chr16: 34,466,691-34,755,828 , GRCh38.p12 chr16: 35,232,320-35,521,457	RARRES2P7, AGGF1P9, 26 more genes
nsv4367404	copy number variation	2	nstd173	human	GRCh37 chr16: 56,663,793-56,724,072 , GRCh38.p12 chr16: 56,629,881-56,690,160	MT1CP, MT1F, 11 more genes

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Number of Variants: 20

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