fam43a[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
nsv3915488	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 185,203,637-197,837,049 , NCBI36 chr3: 186,686,331-199,321,446 , GRCh38 chr3: 185,485,849-198,110,178	FAM43A, SNAR-I, 260 more genes
nsv3920607	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 187,082,628-197,946,692 , GRCh37.p13 chr3: 185,599,934-196,462,295 , GRCh38.p12 chr3: 185,882,146-196,735,424	FAM43A, FGF12, 212 more genes
nsv3872972	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 189,101,446-197,838,262 , GRCh38.p12 chr3: 189,383,657-198,111,391	FAM43A, TMEM44, 187 more genes
nsv6290259	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 189,608,636-197,532,175 , GRCh38.p12 chr3: 189,890,847-197,805,304	FAM43A, LINC01972, 174 more genes
nsv3920718	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 188,646,713-196,231,151 , GRCh37 chr3: 187,164,019-194,749,862 , GRCh38 chr3: 187,446,231-195,029,133	FAM43A, LOC105374283, 105 more genes
nsv6290248	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 191,866,466-197,842,171 , GRCh38.p12 chr3: 192,148,677-198,115,300	FAM43A, PIGZ, 156 more genes
nsv3920444	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 195,540,958-198,905,009 , GRCh38 chr3: 194,338,534-197,693,741 , GRCh37 chr3: 194,059,263-197,420,612	FAM43A, RN7SL36P, 107 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	FAM43A, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	FAM43A, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	FAM43A, RPL23AP49, 2875 more genes
nsv3918981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446	FAM43A, LINC02614, 1469 more genes
nsv3918692	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833	FAM43A, LOC105374179, 785 more genes
nsv3918066	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 152,100,512-198,118,383 , NCBI36 chr3: 153,300,991-199,329,651 , GRCh37 chr3: 151,818,301-197,845,254	FAM43A, LOC105374260, 696 more genes
nsv3918149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 155,836,230-197,851,986 , GRCh38 chr3: 156,118,441-198,125,115 , NCBI36 chr3: 157,318,924-199,336,383	FAM43A, LINC02031, 647 more genes
nsv3913128	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 156,321,878-198,113,452 , NCBI36 chr3: 157,522,361-199,324,720 , GRCh37 chr3: 156,039,667-197,840,323	FAM43A, SNORA4, 644 more genes
nsv3914686	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 158,493,861-199,345,995 , GRCh37 chr3: 157,011,167-197,861,598 , GRCh38 chr3: 157,293,378-198,134,727	FAM43A, RPL34P10, 625 more genes
nsv3871065	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 158,980,631-197,766,890 , GRCh38.p12 chr3: 159,262,842-198,040,019	FAM43A, LINC02048, 599 more genes
nsv3912173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 167,337,691-199,336,383 , GRCh37 chr3: 165,854,997-197,851,986 , GRCh38 chr3: 166,137,209-198,125,115	FAM43A, LOC105374277, 540 more genes
nsv3918982	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 167,885,356-197,837,049 , NCBI36 chr3: 169,368,050-199,321,446 , GRCh38 chr3: 168,167,568-198,110,178	FAM43A, EIF4G1, 515 more genes
nsv3871599	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 173,281,266-197,838,262 , GRCh38.p12 chr3: 173,563,476-198,111,391	FAM43A, LOC105374263, 436 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 47

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Number of Variants: 20

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