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

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Items: 17

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4683080	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 49,457,133-49,457,231 , GRCh38.p12 chr3: 49,419,700-49,419,798	AMT
nsv4682682	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 49,458,915-49,461,781 , GRCh38.p12 chr3: 49,421,482-49,424,348	AMT, NICN1
nsv7096810	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 49,456,384-49,459,947 , GRCh38.p12 chr3: 49,418,951-49,422,514	AMT, NICN1
nsv6311988	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 49,454,201-49,457,785 , GRCh38.p12 chr3: 49,416,768-49,420,352	AMT, TCTA, 1 more genes
nsv6311878	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 49,394,821-49,459,947 , GRCh38.p12 chr3: 49,357,388-49,422,514	AMT, RHOA, 3 more genes
nsv4728146	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 48,807,193-51,363,558 , GRCh38.p12 chr3: 48,769,760-51,326,127	AMT, APEH, 90 more genes
nsv5673729	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 48,507,870-50,340,407 , GRCh38.p12 chr3: 48,466,471-50,302,976	AMT, SEMA3B-AS1, 87 more genes
nsv4674083	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 48,346,677-49,630,228 , GRCh38.p12 chr3: 48,305,187-49,592,795	AMT, MIR6823, 59 more genes
nsv4683411	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 49,158,649-49,570,642 , GRCh38.p12 chr3: 49,121,216-49,533,209	AMT, C3orf84, 15 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	AMT, 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	AMT, 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	AMT, RPL23AP49, 2875 more genes
nsv4347762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589	AMT, UQCRC1, 291 more genes
nsv3921797	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 45,896,379-50,762,357 , GRCh38 chr3: 45,879,883-50,749,922 , GRCh37 chr3: 45,921,375-50,787,353	AMT, RBM5-AS1, 185 more genes
nsv3883164	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 37,028,313-49,929,220 , GRCh38.p12 chr3: 36,986,822-49,891,787	AMT, ACAA1, 344 more genes
nsv6313476	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 49,060,512-49,678,685 , GRCh38.p12 chr3: 49,023,079-49,641,252	AMT, DAG1, 23 more genes
nsv3914130	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 49,183,818-49,487,072 , GRCh38 chr3: 49,171,381-49,474,635 , GRCh37 chr3: 49,208,814-49,512,068	AMT, GPX1, 11 more genes

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amt[All Fields] AND 1[has_clinical] (18)
dbVar
Homo sapiens cytochrome P450, family 4, subfamily V, polypeptide 2 (CYP4V2), mRN...
Homo sapiens cytochrome P450, family 4, subfamily V, polypeptide 2 (CYP4V2), mRNA
gi|61743921|ref|NM_207352.2|

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