ift88[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
nsv3908776	copy number variation	1	nstd102	human	Benign	GRCh37 chr13: 21,219,027-21,245,468 , GRCh38.p12 chr13: 20,644,888-20,671,329	IFT88
nsv7094396	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 21,217,574-21,245,198 , GRCh38.p12 chr13: 20,643,435-20,671,059	IFT88
nsv4455272	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 21,201,901-21,217,306 , GRCh38.p12 chr13: 20,627,762-20,643,167	IFT88
nsv7094236	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 21,199,869-21,200,008 , GRCh38.p12 chr13: 20,625,730-20,625,869	IFT88
nsv7094237	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 21,237,617-21,237,763 , GRCh38.p12 chr13: 20,663,478-20,663,624	IFT88
nsv6137742	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 20,836,960-21,152,070 , GRCh38.p12 chr13: 20,262,821-20,577,931	IFT88, LOC105370103, 3 more genes
nsv7094069	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 21,086,562-21,212,677 , GRCh38.p12 chr13: 20,512,423-20,638,538	IFT88, LOC105370103, 3 more genes
nsv3910270	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,445,862-114,327,173 , NCBI36 chr13: 10,098,739-114,110,750 , GRCh37 chr13: 19,020,001-115,085,141	IFT88, RNU6-71P, 1332 more genes
nsv4675550	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,436,286-24,970,361 , GRCh38.p12 chr13: 18,862,146-24,396,223	IFT88, MRPL57, 129 more genes
nsv3890184	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 20,008,480-25,534,121 , GRCh38.p12 chr13: 19,434,340-24,959,983	IFT88, ANKRD20A19P, 125 more genes
nsv3912021	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 19,144,074-24,458,010 , GRCh38 chr13: 19,671,934-24,985,872 , GRCh37 chr13: 20,246,074-25,560,010	IFT88, TPTE2P1, 119 more genes
nsv4455063	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,436,286-23,274,540 , GRCh38.p12 chr13: 18,862,146-22,700,401	IFT88, SAP18, 90 more genes
nsv6637646	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,436,287-22,089,005 , GRCh38.p12 chr13: 18,862,147-21,514,866	IFT88, LOC105370104, 78 more genes
nsv4456640	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 20,562,171-22,993,375 , GRCh38.p12 chr13: 19,988,031-22,419,236	IFT88, RANP8, 53 more genes
nsv3919995	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 19,206,550-21,596,737 , GRCh37.p13 chr13: 20,308,550-22,698,737 , GRCh38.p12 chr13: 19,734,410-22,124,598	IFT88, CNOT4P1, 56 more genes
nsv4675255	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 20,668,070-23,029,230 , GRCh38.p12 chr13: 20,093,931-22,455,091	IFT88, RPSAP54, 52 more genes
nsv3914641	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 19,885,283-22,014,498 , NCBI36 chr13: 19,357,423-21,486,637 , GRCh37 chr13: 20,459,423-22,588,637	IFT88, LOC105370102, 49 more genes
nsv3916109	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 20,600,790-22,541,928 , GRCh38 chr13: 20,026,650-21,967,789 , NCBI36 chr13: 19,498,790-21,439,928	IFT88, LOC105370103, 49 more genes
nsv6315495	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403	IFT88, RNU6-80P, 1334 more genes
nsv6289999	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403	IFT88, LINC00363, 1334 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 58

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Number of Variants: 20

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Supplemental Content

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