fam180a[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	FAM180A, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	FAM180A, LOC107986817, 2014 more genes
nsv4675615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620	FAM180A, ATG9B, 603 more genes
nsv3915633	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 134,002,121-158,077,335 , GRCh38 chr7: 134,666,829-158,591,882 , GRCh37 chr7: 134,351,581-158,384,574	FAM180A, MOXD2P, 561 more genes
nsv7097864	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959	FAM180A, NOBOX, 466 more genes
nsv6636458	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 131,779,213-149,042,734 , GRCh38.p12 chr7: 132,094,454-149,345,643	FAM180A, TRBD2, 403 more genes
nsv3914137	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 134,702,438-148,504,492 , NCBI36 chr7: 134,352,978-148,135,425 , GRCh38 chr7: 135,017,687-148,807,400	FAM180A, LOC105375537, 348 more genes
nsv3903275	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 127,295,698-139,524,358 , GRCh38.p12 chr7: 127,655,644-139,824,559	FAM180A, RNU6-1272P, 224 more genes
nsv6290262	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 133,848,099-145,814,115 , GRCh38.p12 chr7: 134,163,347-146,117,023	FAM180A, TRBJ2-7, 341 more genes
nsv3910067	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 135,414,108-144,140,219 , NCBI36 chr7: 134,749,397-143,468,245 , GRCh37 chr7: 135,098,857-143,837,312	FAM180A, LOC105375534, 292 more genes
nsv3895502	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 131,642,114-139,107,211 , GRCh38.p12 chr7: 131,957,355-139,422,465	FAM180A, RPS17P12, 106 more genes
nsv3895298	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 133,230,189-137,972,605 , GRCh38.p12 chr7: 133,545,435-138,287,860	FAM180A, AKR1B1, 62 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	FAM180A, RNU6-565P, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	FAM180A, RPL23AP51, 2684 more genes
nsv3909087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620	FAM180A, MNX1-AS2, 2682 more genes
nsv3908592	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017	FAM180A, TRGV3, 2682 more genes
nsv3922815	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 96,887,100-158,409,214 , GRCh38 chr7: 97,419,852-158,923,762 , GRCh37 chr7: 97,049,164-158,716,453	FAM180A, SEPTIN7P6, 1175 more genes
nsv3894097	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 98,693,388-159,119,707 , GRCh38.p12 chr7: 99,095,765-159,327,017	FAM180A, CYP3A5, 1144 more genes
nsv4675620	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017	FAM180A, RPL26P23, 887 more genes
nsv3918979	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 115,099,069-159,118,507 , NCBI36 chr7: 114,886,305-158,811,268 , GRCh38 chr7: 115,459,015-159,325,817	FAM180A, ABCF2, 844 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 35

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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