tent2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4729278	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 78,845,630-79,106,163 , GRCh38.p12 chr5: 79,549,807-79,810,340	TENT2, CMYA5, 1 more genes
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	TENT2, MEGF10, 2080 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	TENT2, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	TENT2, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	TENT2, SPEF2, 2490 more genes
nsv3917856	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 74,163,186-110,809,453 , NCBI36 chr5: 73,494,767-110,173,052 , GRCh37 chr5: 73,459,011-110,145,153	TENT2, CSNK1A1P3, 413 more genes
nsv4675667	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166	TENT2, LOC101929380, 318 more genes
nsv3874970	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 78,573,790-78,909,324 , GRCh38.p12 chr5: 79,277,967-79,613,501	TENT2, LOC101929201, 8 more genes
nsv4436202	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379	TENT2, RNU1-150P, 1757 more genes
nsv3914496	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 78,961,491-80,493,505 , NCBI36 chr5: 78,997,247-80,529,261 , GRCh38 chr5: 79,665,668-81,197,686	TENT2, ZFYVE16, 31 more genes
nsv6636260	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 77,746,948-79,089,197 , GRCh38.p12 chr5: 78,451,125-79,793,374	TENT2, RPL29P15, 18 more genes
nsv4456095	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 78,687,874-79,208,782 , GRCh38.p12 chr5: 79,392,051-79,912,959	TENT2, CMYA5, 7 more genes
nsv3912593	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259	TENT2, LOC105378993, 2492 more genes
nsv4675682	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 78,094,810-78,936,391 , GRCh38.p12 chr5: 78,798,987-79,640,568	TENT2, LOC107986426, 14 more genes
nsv3922603	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 78,135,940-78,951,758 , GRCh38 chr5: 78,804,361-79,620,179 , GRCh37 chr5: 78,100,184-78,916,002	TENT2, BHMT2, 14 more genes
nsv4455617	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 78,700,197-79,294,390 , GRCh38.p12 chr5: 79,404,374-79,998,567	TENT2, LOC102724557, 10 more genes

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tent2[All Fields] AND 1[has_clinical] (17)
dbVar
Homo sapiens tumor protein D52 (TPD52), transcript variant 11, non-coding RNA
Homo sapiens tumor protein D52 (TPD52), transcript variant 11, non-coding RNA
gi|1708260725|ref|NR_105036.2|

Nucleotide

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