fam13a[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
nsv6315137	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 88,928,831-88,996,847 , GRCh37.p13 chr4: 89,849,982-89,917,998	FAM13A, LOC105377327
nsv6290923	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr4: 89,782,569-89,849,657 , GRCh38.p12 chr4: 88,861,418-88,928,506	FAM13A, LOC105377327
nsv3877008	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 89,811,514-89,938,991 , GRCh38.p12 chr4: 88,890,363-89,017,840	FAM13A, LOC105377327
nsv3923932	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 90,030,703-90,232,138 , GRCh37.p13 chr4: 89,811,680-90,013,115 , GRCh38.p12 chr4: 88,890,529-89,091,964	FAM13A, LOC105377327
nsv3882273	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 89,625,427-89,756,076 , GRCh38.p12 chr4: 88,704,276-88,834,925	FAM13A, HERC3, 1 more genes
nsv3923759	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 58,862,002-102,129,682 , GRCh37.p13 chr4: 59,167,245-101,910,659 , GRCh38.p12 chr4: 58,301,079-100,989,502	FAM13A, EREG, 530 more genes
nsv3923733	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 80,427,023-100,855,441 , GRCh37 chr4: 81,348,177-101,776,598 , NCBI36 chr4: 81,567,201-101,995,621	FAM13A, PDLIM5, 215 more genes
nsv7148241	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930	FAM13A, LOC105377327, 214 more genes
nsv3888958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 81,314,915-96,636,651 , GRCh38.p12 chr4: 80,393,761-95,715,500	FAM13A, LOC391674, 156 more genes
nsv6313484	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 79,780,152-94,873,225 , GRCh38.p12 chr4: 78,858,998-93,952,074	FAM13A, LOC105377329, 166 more genes
nsv3912429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 81,800,931-95,730,598 , NCBI36 chr4: 82,019,955-95,949,621 , GRCh38 chr4: 80,879,777-94,809,447	FAM13A, RNU6-469P, 152 more genes
nsv6291249	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 80,467,886-93,362,064 , GRCh38.p12 chr4: 79,546,732-92,440,913	FAM13A, HNRNPA3P13, 155 more genes
nsv3916835	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 80,496,902-93,333,600 , GRCh38 chr4: 79,575,748-92,412,449 , NCBI36 chr4: 80,715,926-93,552,623	FAM13A, SLC10A6, 155 more genes
nsv4436731	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 80,482,400-92,572,499 , GRCh38.p12 chr4: 79,561,246-91,651,348	FAM13A, HERC5, 150 more genes
nsv6313848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 81,054,789-90,667,421 , GRCh38.p12 chr4: 80,133,635-89,746,270	FAM13A, RPL6P13, 136 more genes
nsv3915919	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 85,469,728-94,794,648 , GRCh37.p13 chr4: 85,250,704-94,575,625 , GRCh38.p12 chr4: 84,329,551-93,654,474	FAM13A, RNU6-907P, 89 more genes
nsv3910328	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 86,370,518-94,894,345 , GRCh38 chr4: 85,449,365-93,973,194 , NCBI36 chr4: 86,589,542-95,113,368	FAM13A, LOC112268468, 81 more genes
nsv3875754	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 82,283,358-90,341,831 , GRCh38.p12 chr4: 81,362,204-89,420,680	FAM13A, LOC152845, 121 more genes
nsv3883611	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 85,839,771-93,071,150 , GRCh38.p12 chr4: 84,918,618-92,149,999	FAM13A, HERC5, 78 more genes
nsv3888291	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 90,005,204-96,971,785 , GRCh38.p12 chr4: 89,084,053-96,050,634	FAM13A, HMGB3P15, 33 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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