hmgcll1[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
nsv3888415	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 55,415,479-55,417,477 , GRCh38.p12 chr6: 55,550,681-55,552,679	HMGCLL1
nsv4456729	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 55,388,285-55,506,553 , GRCh38.p12 chr6: 55,523,487-55,641,755	HMGCLL1
nsv4729027	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 55,310,852-55,396,953 , GRCh38.p12 chr6: 55,446,054-55,532,155	HMGCLL1
nsv6291289	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 55,328,665-55,378,845 , GRCh38.p12 chr6: 55,463,867-55,514,047	HMGCLL1
nsv3912119	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 55,452,087-55,773,417 , GRCh37.p13 chr6: 55,344,128-55,665,458 , GRCh38.p12 chr6: 55,479,330-55,800,660	HMGCLL1, BMP5
nsv3911517	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 55,324,406-55,508,208 , GRCh37.p13 chr6: 55,216,447-55,400,249 , GRCh38.p12 chr6: 55,351,649-55,535,451	HMGCLL1, GFRAL
nsv4457198	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 55,053,759-55,499,082 , GRCh38.p12 chr6: 55,188,961-55,634,284	HMGCLL1, GFRAL, 1 more genes
nsv6636647	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 54,926,500-55,647,880 , GRCh38.p12 chr6: 55,061,702-55,783,082	HMGCLL1, HCRTR2, 2 more genes
nsv3922315	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 50,938,895-57,297,586 , NCBI36 chr6: 51,046,854-57,405,545 , GRCh38 chr6: 50,971,182-57,432,788	HMGCLL1, MLIP-AS1, 100 more genes
nsv3923753	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 54,263,893-56,826,637 , GRCh37 chr6: 54,128,691-56,691,435 , NCBI36 chr6: 54,236,650-56,799,394	HMGCLL1, RNU6-1023P, 20 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	HMGCLL1, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	HMGCLL1, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	HMGCLL1, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	HMGCLL1, ITPR3, 2905 more genes
nsv4350067	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650	HMGCLL1, HLA-DPB2, 1001 more genes
nsv3915840	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 53,931,543-68,149,750 , GRCh37 chr6: 53,796,341-68,859,642 , NCBI36 chr6: 53,904,300-68,916,363	HMGCLL1, LOC442225, 104 more genes
nsv4729270	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 48,626,041-55,575,545 , GRCh38.p12 chr6: 48,658,305-55,710,747	HMGCLL1, CRISP1, 105 more genes
nsv6314749	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313	HMGCLL1, ACTG1P9, 245 more genes
nsv3870556	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr6: 54,730,810-56,217,129 , GRCh38.p12 chr6: 54,866,012-56,352,331	HMGCLL1, DHFRP6, 8 more genes
nsv6638066	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr6: 53,151,508-58,400,428 , GRCh37.p13 chr6: 53,016,306-58,726,706	HMGCLL1, NPM1P36, 73 more genes

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Items: 20

Number of Variants: 20

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