polk[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3888072	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 6,712,533-6,734,625 , GRCh38.p12 chr5: 6,712,420-6,734,512	TENT4A
nsv3886266	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 6,713,140-6,734,625 , GRCh38.p12 chr5: 6,713,027-6,734,512	TENT4A
nsv3880474	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 6,692,053-6,714,662 , GRCh38.p12 chr5: 6,691,940-6,714,549	LINC02102, TENT4A
nsv4675251	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 74,736,232-74,822,073 , GRCh38.p12 chr5: 75,440,407-75,526,248	POLK, CERT1
nsv3878369	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 74,734,502-74,937,724 , GRCh38.p12 chr5: 75,438,677-75,641,899	POLK, RNU7-175P, 2 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	POLK, MEGF10, 2080 more genes
nsv3914649	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 22,149-35,831,538 , GRCh37 chr5: 22,149-35,831,640 , NCBI36 chr5: 75,149-35,867,397	LOC105374666, CCNB3P1, 399 more genes
nsv3887142	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-34,041,196 , GRCh38.p12 chr5: 22,149-34,041,091	H3Y1, CTD-2350J17.1, 381 more genes
nsv3910712	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 166,576-34,034,151 , GRCh38 chr5: 113,461-33,998,289 , GRCh37 chr5: 113,576-33,998,394	ROPN1L, RN7SKP73, 378 more genes
nsv3924496	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-32,248,116 , NCBI36 chr5: 75,149-32,283,873 , GRCh38 chr5: 22,149-32,248,010	LOC105374678, MIR4278, 356 more genes
nsv6636942	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932	LOC105374608, LSP1P3, 351 more genes
nsv6636606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-31,448,527 , GRCh38.p12 chr5: 113,462-31,448,420	BASP1, RNU1-76P, 338 more genes
nsv3881706	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-31,343,671 , GRCh38.p12 chr5: 25,329-31,343,564	IRX2-DT, CEP72-DT, 339 more genes
nsv3883796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-30,672,798 , GRCh38.p12 chr5: 25,329-30,672,691	H3P22, PDCD6-AHRR, 335 more genes
nsv6315416	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-30,712,376 , GRCh38.p12 chr5: 113,461-30,712,269	LOC105374649, LINC02196, 333 more genes
nsv3912696	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 50,093-30,112,642 , GRCh38 chr5: 49,978-30,112,535 , NCBI36 chr5: 103,093-30,148,399	OTULINL, LINC02111, 333 more genes
nsv5381771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716	OTULINL, AKTIPP2, 317 more genes
nsv3916877	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-28,625,056 , GRCh37 chr5: 22,149-28,589,299 , GRCh38 chr5: 22,149-28,589,192	CTD-2154B17.1, MIR10397, 313 more genes
nsv3922865	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 22,149-28,429,241 , GRCh37 chr5: 22,149-28,429,348 , NCBI36 chr5: 75,149-28,465,105	CCT6P2, LOC105374661, 312 more genes
nsv3916127	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-27,824,480 , GRCh37 chr5: 22,149-27,788,723 , GRCh38 chr5: 22,149-27,788,616	LOC101929898, ZDHHC11, 310 more genes

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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

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 106

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Number of Variants: 20

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