jpt2[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
nsv3897848	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 1,564,823-1,743,511 , GRCh38.p12 chr16: 1,514,822-1,693,510	JPT2, IFT140, 3 more genes
nsv4456545	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 1,719,218-1,758,761 , GRCh38.p12 chr16: 1,669,217-1,708,760	JPT2, MAPK8IP3, 1 more genes
nsv4455594	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-2,053,328 , GRCh38.p12 chr16: 35,880-2,003,327	JPT2, TSR3, 128 more genes
nsv3919589	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 36,766-1,987,584 , GRCh37 chr16: 96,766-2,047,583 , GRCh38 chr16: 46,766-1,997,582	JPT2, C1QTNF8, 127 more genes
nsv3914731	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 46,722-1,867,327 , NCBI36 chr16: 36,722-1,857,329 , GRCh37 chr16: 96,722-1,917,328	JPT2, TPSP2, 110 more genes
nsv3897602	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-1,875,694 , GRCh38.p12 chr16: 35,880-1,825,693	JPT2, CHTF18, 110 more genes
nsv3919625	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 23,141-1,773,349 , NCBI36 chr16: 13,141-1,763,351 , GRCh37 chr16: 73,141-1,823,350	JPT2, RHOT2, 106 more genes
nsv3916129	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 13,141-1,702,525 , GRCh38 chr16: 23,141-1,712,523 , GRCh37 chr16: 73,141-1,762,524	JPT2, C4orf46P1, 102 more genes
nsv4683390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 624,055-2,148,005 , GRCh38.p12 chr16: 574,055-2,098,004	JPT2, MRPS34, 102 more genes
nsv4449893	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 624,055-2,115,656 , GRCh38.p12 chr16: 574,055-2,065,655	JPT2, LMF1-AS1, 99 more genes
nsv7098880	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 811,896-2,130,379 , GRCh38.p12 chr16: 761,896-2,080,378	JPT2, TPSP1, 78 more genes
nsv4683209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 1,203,718-2,185,710 , GRCh38.p12 chr16: 1,153,718-2,135,709	JPT2, TMEM204, 67 more genes
nsv3893007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 1,734,363-2,285,561 , GRCh38.p12 chr16: 1,684,362-2,235,560	JPT2, IGFALS, 49 more genes
nsv4682253	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 1,573,499-2,114,448 , GRCh38.p12 chr16: 1,523,498-2,064,447	JPT2, NHERF2, 37 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	JPT2, 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	JPT2, 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	JPT2, 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	JPT2, 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	JPT2, FTLP14, 1868 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	JPT2, BMERB1, 701 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 56

Page of 3

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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