tk1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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	TK1, PRPSAP1, 1350 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	TK1, 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	TK1, 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	TK1, 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	TK1, 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	TK1, 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	TK1, FOXK2, 958 more genes
nsv4457646	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062	TK1, LOC107985089, 448 more genes
nsv3909523	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 63,689,671-81,041,938 , GRCh38.p12 chr17: 65,693,553-83,084,062	TK1, RPL38, 428 more genes
nsv3906075	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 67,002,415-81,041,938 , GRCh38.p12 chr17: 69,006,274-83,084,062	TK1, CEP131, 374 more genes
nsv3917654	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 64,716,815-78,637,842 , GRCh37 chr17: 67,205,220-81,044,553 , GRCh38 chr17: 69,209,079-83,086,677	TK1, LOC101928447, 368 more genes
nsv3919156	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 69,916,435-83,102,552 , GRCh37 chr17: 67,912,576-81,048,189 , NCBI36 chr17: 65,424,171-78,653,717	TK1, CD300A, 359 more genes
nsv6315182	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323	TK1, DUS1L, 252 more genes
nsv3897835	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 73,951,701-81,041,938 , GRCh38.p12 chr17: 75,955,620-83,084,062	TK1, ARHGDIA, 230 more genes
nsv4676104	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963	TK1, LLGL2, 165 more genes
nsv3919635	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 76,088,317-81,044,553 , NCBI36 chr17: 73,599,912-78,637,842 , GRCh38 chr17: 78,092,236-83,086,677	TK1, LINC03048, 154 more genes
nsv3911899	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr17: 78,092,356-78,444,214 , NCBI36 chr17: 73,600,032-73,951,891 , GRCh37 chr17: 76,088,437-76,440,296	TK1, SOCS3, 17 more genes

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tk1[All Fields] AND 1[has_clinical] (18)
dbVar
GEO Profile Links for Gene (Select 10017) (1000)
GEO Profiles
MedGen for Gene (Select 6311) (2)
MedGen
Taxonomy Links for Gene (Select 6311) (1)
Taxonomy
Homo sapiens chromosome 16 open reading frame 45, mRNA (cDNA clone MGC:4532 IMAG...
Homo sapiens chromosome 16 open reading frame 45, mRNA (cDNA clone MGC:4532 IMAGE:3010666), complete cds
gi|33870955|gb|BC008967.2|

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