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

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Items: 18

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	ADO, RNU7-12P, 1876 more genes
nsv4675455	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 50,250,603-69,256,083 , GRCh38.p12 chr10: 45,931,517-67,496,325	ADO, MRLN, 242 more genes
nsv3922335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 60,196,226-76,174,974 , GRCh38 chr10: 58,436,466-74,415,216 , NCBI36 chr10: 59,866,232-75,844,980	ADO, UNC5B-AS1, 250 more genes
nsv4675436	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 56,031,210-65,660,398 , GRCh38.p12 chr10: 54,271,450-63,900,638	ADO, MRPL35P2, 77 more genes
nsv3906389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996	ADO, LOC100419870, 2105 more genes
nsv3891157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558	ADO, AGAP14P, 2097 more genes
nsv3902271	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639	ADO, ANXA11, 2085 more genes
nsv3891958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414	ADO, TUBB8, 2085 more genes
nsv7137211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639	ADO, EXOC6, 1906 more genes
nsv3924859	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961	ADO, BMS1P4-AGAP5, 471 more genes
nsv3917047	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 42,500,760-75,145,672 , GRCh37 chr10: 43,180,754-75,475,666 , GRCh38 chr10: 42,685,306-73,715,908	ADO, SLC9A3P3, 476 more genes
nsv3921181	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 41,927,641-68,830,439 , GRCh38 chr10: 42,112,187-67,400,675 , GRCh37 chr10: 42,607,635-69,160,433	ADO, AGAP6, 338 more genes
nsv3919727	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 55,287,177-67,558,442 , GRCh37 chr10: 57,046,937-69,318,200 , NCBI36 chr10: 56,716,943-68,988,206	ADO, RNU6-543P, 96 more genes
nsv3907664	copy number variation	1	nstd102	human	drug response	GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422	ADO, SHOC2, 1487 more genes
nsv6637363	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 57,941,252-64,846,332 , GRCh38.p12 chr10: 56,181,491-63,086,572	ADO, TMEM26-AS1, 53 more genes
nsv4674969	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 62,191,184-65,348,431 , GRCh38.p12 chr10: 60,431,426-63,588,671	ADO, RNU6-543P, 33 more genes
nsv3921516	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr10: 60,977,777-62,913,465 , NCBI36 chr10: 62,407,541-64,343,231 , GRCh37 chr10: 62,737,535-64,673,225	ADO, ZNF365, 16 more genes
nsv3896400	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 63,888,935-64,783,617 , GRCh38.p12 chr10: 62,129,176-63,023,857	ADO, RTKN2, 8 more genes

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ado[All Fields] AND 1[has_clinical] (19)
dbVar
chromosomal replication initiator protein DnaA, partial [Leuconostoc mesenteroid...
chromosomal replication initiator protein DnaA, partial [Leuconostoc mesenteroides]
gi|763712495|gb|AJQ30632.1|

Protein
Homo sapiens DNAJC25-GNG10 readthrough (DNAJC25-GNG10), mRNA
Homo sapiens DNAJC25-GNG10 readthrough (DNAJC25-GNG10), mRNA
gi|1677530191|ref|NM_004125.4|

Nucleotide
ZNF483 zinc finger protein 483 [Homo sapiens]
ZNF483 zinc finger protein 483 [Homo sapiens]
Gene ID:158399

Gene
PTBP3 polypyrimidine tract binding protein 3 [Homo sapiens]
PTBP3 polypyrimidine tract binding protein 3 [Homo sapiens]
Gene ID:9991

Gene

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