lrrc14b[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
nsv3889923	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 22,149-195,335 , GRCh38.p12 chr5: 22,149-195,220	LRRC14B, CCDC127, 3 more genes
nsv3920475	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr5: 75,149-245,836 , GRCh37 chr5: 22,149-192,836 , GRCh38 chr5: 22,149-192,721	LRRC14B, LOC105374602, 2 more genes
nsv3879663	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 136,501-237,633 , GRCh38.p12 chr5: 136,386-237,518	LRRC14B, PLEKHG4B, 2 more genes
nsv3880866	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 151,638-235,584 , GRCh38.p12 chr5: 151,523-235,469	LRRC14B, PLEKHG4B, 2 more genes
nsv3923454	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr5: 151,622-234,045 , GRCh37 chr5: 151,737-234,160 , NCBI36 chr5: 204,737-287,160	LRRC14B, PLEKHG4B, 2 more genes
nsv3879077	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 167,219-204,849 , GRCh38.p12 chr5: 167,104-204,734	LRRC14B, PLEKHG4B, 1 more genes
nsv3924781	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 75,149-245,773 , GRCh37.p13 chr5: 22,149-192,773 , GRCh38.p12 chr5: 22,149-192,658	LRRC14B, PLEKHG4B, 2 more genes
nsv4456649	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 136,735-238,729 , GRCh38.p12 chr5: 136,620-238,614	LRRC14B, PLEKHG4B, 2 more genes
nsv3918705	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 216,452-309,242 , GRCh37.p13 chr5: 163,452-256,242 , GRCh38.p12 chr5: 163,337-256,127	LRRC14B, CCDC127, 2 more genes
nsv3918514	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 225,441-309,242 , GRCh37.p13 chr5: 172,441-256,242 , GRCh38.p12 chr5: 172,326-256,127	LRRC14B, SDHA, 2 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	LRRC14B, LOC105374666, 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	LRRC14B, H3Y1, 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	LRRC14B, ROPN1L, 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	LRRC14B, LOC105374678, 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	LRRC14B, LOC105374608, 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	LRRC14B, BASP1, 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	LRRC14B, IRX2-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	LRRC14B, H3P22, 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	LRRC14B, LOC105374649, 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	LRRC14B, OTULINL, 333 more genes

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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 150

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Number of Variants: 20

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