fut5[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	FUT5, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	FUT5, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	FUT5, LENG8, 2408 more genes
nsv3914351	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555	FUT5, SEMA6B, 299 more genes
nsv3924102	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622	FUT5, POLR2E, 283 more genes
nsv3890584	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 3,120,160-9,732,820 , GRCh38.p12 chr19: 3,120,162-9,622,144	FUT5, PCP2, 250 more genes
nsv3923313	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 4,934,897-6,501,653 , GRCh38 chr19: 4,934,885-6,501,642 , NCBI36 chr19: 4,885,897-6,452,653	FUT5, LOC105372253, 47 more genes
nsv3904954	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 5,455,422-5,995,450 , GRCh38.p12 chr19: 5,455,411-5,995,439	FUT5, NDUFA11, 22 more genes
nsv3893558	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 5,823,903-6,175,936 , GRCh38.p12 chr19: 5,823,892-6,175,925	FUT5, FUT3, 12 more genes
nsv3907907	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 5,655,792-5,867,913 , GRCh38.p12 chr19: 5,655,781-5,867,902	FUT5, NRTN, 12 more genes
nsv3924480	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr19: 5,401,983-6,486,595 , GRCh37.p13 chr19: 5,450,983-6,535,595 , GRCh38.p12 chr19: 5,450,972-6,535,584	FUT5, TINCR, 42 more genes
nsv3913242	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr19: 5,586,385-5,818,934 , GRCh37.p13 chr19: 5,635,385-5,867,934 , GRCh38.p12 chr19: 5,635,374-5,867,923	FUT5, FUT3, 12 more genes
nsv6314807	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 5,678,562-5,903,719 , GRCh38.p12 chr19: 5,678,551-5,903,708	FUT5, VMAC, 13 more genes
nsv6310708	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 5,678,562-5,897,028 , GRCh38.p12 chr19: 5,678,551-5,897,017	FUT5, DUS3L, 12 more genes

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