Gene Links for dbVar (Select 52879782) - Gene

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Links from dbVar

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Name/Gene ID	Description	Location	Aliases
Select item 109623477 SNORD163 ID: 109623477	small nucleolar RNA, C/D box 163 [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (16153133..16153196, complement)
Select item 107985051 LOC107985051 ID: 107985051	uncharacterized LOC107985051 [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (18609633..18615900)
Select item 107984989 LOC107984989 ID: 107984989	uncharacterized LOC107984989 [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (17977556..17989814, complement)
Select item 106865374 RNU6-468P ID: 106865374	RNA, U6 small nuclear 468, pseudogene [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (17578631..17578738)
Select item 106481920 RNU6-862P ID: 106481920	RNA, U6 small nuclear 862, pseudogene [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (16137768..16137872, complement)
Select item 106481916 RNU6-767P ID: 106481916	RNA, U6 small nuclear 767, pseudogene [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (17170083..17170189)
Select item 106481859 RN7SL775P ID: 106481859	RNA, 7SL, cytoplasmic 775, pseudogene [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (17178414..17178749)
Select item 106481688 YWHAEP2 ID: 106481688	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon pseudogene 2 [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (18418195..18418306, complement)
Select item 106481278 RNU6-314P ID: 106481278	RNA, U6 small nuclear 314, pseudogene [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (16098704..16098807)
Select item 106481043 RN7SL442P ID: 106481043	RNA, 7SL, cytoplasmic 442, pseudogene [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (16191832..16192151)
Select item 106479744 RNU6-405P ID: 106479744	RNA, U6 small nuclear 405, pseudogene [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (16691798..16691907)
Select item 106479448 RN7SL620P ID: 106479448	RNA, 7SL, cytoplasmic 620, pseudogene [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (16710063..16710361)
Select item 105371570 LOC105371570 ID: 105371570	uncharacterized LOC105371570 [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (18438452..18440057, complement)
Select item 105371569 LOC105371569 ID: 105371569	uncharacterized LOC105371569 [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (18442208..18448764, complement)
Select item 105371567 LOC105371567 ID: 105371567	uncharacterized LOC105371567 [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (18153201..18155340, complement)
Select item 105371566 LOC105371566 ID: 105371566	uncharacterized LOC105371566 [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (18107691..18117561, complement)
Select item 105371564 SMCR2 ID: 105371564	Smith-Magenis syndrome chromosome region, candidate 2 [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (17674026..17677688, complement)	TCONS_00025215
Select item 105371562 LINC02090 ID: 105371562	long intergenic non-protein coding RNA 2090 [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (16988329..16990176)
Select item 105371559 LOC105371559 ID: 105371559	uncharacterized LOC105371559 [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (15744638..15764598, complement)
Select item 105371557 LOC105371557 ID: 105371557	uncharacterized LOC105371557 [Homo sapiens (human)]	Chromosome 17, NC_000017.11 (15831512..15847878, complement)