spop[All Fields] AND 1[has_clinical] - dbVar

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Items: 13

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4676234	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 47,689,783-47,791,730 , GRCh38.p12 chr17: 49,612,421-49,714,368	SPOP, LOC107984999, 2 more genes
nsv3911811	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577	SPOP, PRPSAP1, 1350 more genes
nsv3912763	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 44,570,225-47,580,169 , GRCh37 chr17: 47,215,226-50,225,170 , GRCh38 chr17: 49,137,864-52,147,810	SPOP, CACNA1G, 77 more genes
nsv3921455	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 44,793,516-45,701,800 , GRCh37 chr17: 47,438,517-48,346,801 , GRCh38 chr17: 49,361,155-50,269,440	SPOP, DLX4, 32 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	SPOP, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	SPOP, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	SPOP, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	SPOP, SMURF2, 2366 more genes
nsv3914783	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577	SPOP, LOC105371922, 1855 more genes
nsv3909511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846	SPOP, FOXK2, 958 more genes
nsv3913552	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225	SPOP, RNU6-131P, 1075 more genes
nsv3911563	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214	SPOP, PLEKHH3, 958 more genes
nsv3890215	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 46,481,089-51,396,368 , GRCh38.p12 chr17: 48,403,727-53,319,007	SPOP, ATP5MC1, 124 more genes

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spop[All Fields] AND 1[has_clinical] (14)
dbVar
MIR6894 microRNA 6894 [Homo sapiens]
MIR6894 microRNA 6894 [Homo sapiens]
Gene ID:102466759

Gene
MAP kinase-activated protein kinase 5 isoform 2 [Rattus norvegicus]
MAP kinase-activated protein kinase 5 isoform 2 [Rattus norvegicus]
gi|255708409|ref|NP_001020932.2|

Protein
xl11034C09F_1351702 Xenopus ORFeome version 1.0 library Xenopus laevis cDNA clon...
xl11034C09F_1351702 Xenopus ORFeome version 1.0 library Xenopus laevis cDNA clone xl11034C09 5', mRNA sequence
gi|798031635|gnl|dbEST|79644452|gb| 750.1|

Nucleotide
xl11023E01R_1375969 Xenopus ORFeome version 1.0 library Xenopus laevis cDNA clon...
xl11023E01R_1375969 Xenopus ORFeome version 1.0 library Xenopus laevis cDNA clone xl11023E01 3', mRNA sequence
gi|798036566|gnl|dbEST|79647954|gb| 252.1|

Nucleotide

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