ankrd27[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6314015	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 33,146,131-33,251,180 , GRCh38.p12 chr19: 32,655,225-32,760,274	ANKRD27, RN7SL789P, 3 more genes
nsv3919296	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723	ANKRD27, UBA2, 241 more genes
nsv3916007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990	ANKRD27, MAG, 238 more genes
nsv3918197	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 31,367,353-35,417,098 , NCBI36 chr19: 36,550,099-40,599,840 , GRCh37 chr19: 31,858,259-35,908,000	ANKRD27, LINC01531, 110 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	ANKRD27, 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	ANKRD27, 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	ANKRD27, LENG8, 2408 more genes
nsv3913730	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354	ANKRD27, BCKDHA, 1102 more genes
nsv6290300	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324	ANKRD27, ZNF420, 574 more genes
nsv4457372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575	ANKRD27, ZNF461, 735 more genes
nsv3914228	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 17,148,576-40,106,894 , GRCh38 chr19: 17,176,767-34,924,150 , GRCh37 chr19: 17,287,576-35,415,054	ANKRD27, LOC105372355, 411 more genes
nsv3900139	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 30,735,448-36,120,396 , GRCh38.p12 chr19: 30,244,541-35,629,494	ANKRD27, ZNF599, 130 more genes
nsv3910687	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr19: 32,469,643-32,843,761 , NCBI36 chr19: 37,652,389-38,026,507 , GRCh37 chr19: 32,960,549-33,334,667	ANKRD27, RGS9BP, 9 more genes
nsv3919618	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr19: 32,962,986-39,966,686 , GRCh38 chr19: 27,780,238-34,783,942 , GRCh37 chr19: 28,271,146-35,274,846	ANKRD27, LINC00906, 112 more genes
nsv6314074	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 32,827,535-35,263,640 , GRCh38.p12 chr19: 32,336,629-34,772,735	ANKRD27, LOC100130632, 59 more genes

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ankrd27[All Fields] AND 1[has_clinical] (16)
dbVar
European_Survey_of_Carbapenemase_producing_Enterobacteriaceae__EuSCAPE__Sequenci...
European_Survey_of_Carbapenemase_producing_Enterobacteriaceae__EuSCAPE__Sequencing_Project
European_Survey_of_Carbapenemase_producing_Enterobacteriaceae__EuSCAPE__Sequencing_Project

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BioProject Links for Protein (Select 1453336575) (1)
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