lrch3[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
nsv4728760	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 197,534,958-197,608,162 , GRCh38.p12 chr3: 197,808,087-197,881,291	LRCH3, RPL17P18, 1 more genes
nsv3920769	copy number variation	1	nstd102	human	Benign	GRCh38 chr3: 197,786,508-197,876,465 , NCBI36 chr3: 198,997,776-199,087,733 , GRCh37 chr3: 197,513,379-197,603,336	LRCH3, LOC105374310, 2 more genes
nsv6291128	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 197,386,180-197,532,716 , GRCh38.p12 chr3: 197,659,309-197,805,845	LRCH3, FYTTD1, 2 more genes
nsv4674575	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 197,608,161-197,660,039 , GRCh38.p12 chr3: 197,881,290-197,933,168	LRCH3, IQCG, 1 more genes
nsv4728460	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 197,401,121-197,563,460 , GRCh38.p12 chr3: 197,674,250-197,836,589	LRCH3, RUBCN, 3 more genes
nsv3920314	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 199,073,971-199,195,123 , GRCh37.p13 chr3: 197,589,574-197,710,726 , GRCh38.p12 chr3: 197,862,703-197,983,855	LRCH3, RNU6-858P, 3 more genes
nsv6315046	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr3: 197,836,848-197,925,758 , GRCh37.p13 chr3: 197,563,719-197,652,629	LRCH3, IQCG, 3 more genes
nsv3919344	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 199,073,971-199,146,299 , GRCh37.p13 chr3: 197,589,574-197,661,902 , GRCh38.p12 chr3: 197,862,703-197,935,031	LRCH3, IQCG, 1 more genes
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	LRCH3, SNAR-I, 260 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	LRCH3, 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	LRCH3, LINC01972, 174 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	LRCH3, PIGZ, 156 more genes
nsv7148251	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 197,681,032-198,111,976 , GRCh37.p13 chr3: 197,407,903-197,838,847	LRCH3, RNU6-621P, 12 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	LRCH3, 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	LRCH3, 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	LRCH3, 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	LRCH3, 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	LRCH3, 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	LRCH3, 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	LRCH3, LINC02031, 647 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 69

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Number of Variants: 20

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