arih2[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
nsv3876832	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 48,957,907-48,958,835 , GRCh38.p12 chr3: 48,920,474-48,921,402	ARIH2
nsv3879478	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 48,958,085-48,958,835 , GRCh38.p12 chr3: 48,920,652-48,921,402	ARIH2
nsv3884405	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 48,958,097-48,958,835 , GRCh38.p12 chr3: 48,920,664-48,921,402	ARIH2
nsv3874529	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 48,958,397-48,958,835 , GRCh38.p12 chr3: 48,920,964-48,921,402	ARIH2
nsv3881378	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 48,948,980-48,958,835 , GRCh38.p12 chr3: 48,911,547-48,921,402	ARIH2, ARIH2OS
nsv6315166	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376	ARIH2, TMEM89, 129 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	ARIH2, 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	ARIH2, 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	ARIH2, MIR6823, 59 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	ARIH2, 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	ARIH2, 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	ARIH2, 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	ARIH2, 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	ARIH2, 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	ARIH2, ACAA1, 344 more genes
nsv7096805	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318	ARIH2, SNORA94, 120 more genes
nsv3918356	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 48,988,118-49,208,814 , GRCh38 chr3: 48,950,685-49,171,381 , NCBI36 chr3: 48,963,122-49,183,818	ARIH2, USP19, 15 more genes

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