clec19a[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
nsv3910790	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr16: 19,137,142-19,245,386 , GRCh37.p13 chr16: 19,229,641-19,337,885 , GRCh38.p12 chr16: 19,218,319-19,326,563	CLEC19A, LOC105371114, 1 more genes
nsv3906108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224	CLEC19A, CKLF, 1882 more genes
nsv3904593	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973	CLEC19A, LOC100128079, 1879 more genes
nsv3901410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287	CLEC19A, LINC02175, 1877 more genes
nsv3909417	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867	CLEC19A, PRSS53, 1868 more genes
nsv3892266	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654	CLEC19A, FTLP14, 1868 more genes
nsv4685985	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630	CLEC19A, LOC105371069, 654 more genes
nsv1398297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 102,839-28,327,676 , GRCh38.p12 chr16: 52,839-28,316,355	CLEC19A, BMERB1, 701 more genes
nsv4729901	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272	CLEC19A, NPIPB9, 597 more genes
nsv6637429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029	CLEC19A, MIR6511B2, 535 more genes
nsv3910441	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 4,634,894-29,089,642 , GRCh37 chr16: 4,694,893-29,182,141 , GRCh38 chr16: 4,644,892-29,170,820	CLEC19A, LOC729945, 450 more genes
nsv3903116	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-22,442,007 , GRCh38.p12 chr16: 35,880-22,430,686	CLEC19A, NPIPA8, 616 more genes
nsv3900978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-19,806,921 , GRCh38.p12 chr16: 35,880-19,795,599	CLEC19A, LOC105371091, 543 more genes
nsv3917409	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 14,956,252-28,225,665 , GRCh37 chr16: 15,048,751-28,318,164 , GRCh38 chr16: 14,954,894-28,306,843	CLEC19A, SLC7A5P2, 251 more genes
nsv3896782	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 18,238,275-30,177,240 , GRCh38.p12 chr16: 18,144,418-30,165,919	CLEC19A, SMG1P4, 287 more genes
nsv4436312	complex substitution	1	nstd102	human	Pathogenic	GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558	CLEC19A, ABAT, 876 more genes
nsv3914180	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr16: 18,639,562-19,206,712 , GRCh37.p13 chr16: 18,732,061-19,299,211 , GRCh38.p12 chr16: 18,720,739-19,287,889	CLEC19A, SYT17, 11 more genes
nsv3895762	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 9,273,328-89,548,493 , GRCh38.p12 chr16: 9,179,471-89,482,085	CLEC19A, HERC2P5, 1497 more genes
nsv1398399	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 1,279,324-31,926,800 , GRCh38.p12 chr16: 1,229,323-31,915,479	CLEC19A, FLYWCH2, 817 more genes
nsv3919358	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr16: 18,759,489-19,293,402 , NCBI36 chr16: 18,678,312-19,212,225 , GRCh37 chr16: 18,770,811-19,304,724	CLEC19A, TMC7, 11 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 21

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Number of Variants: 20

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