bmp5[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
nsv4455429	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 55,517,952-55,642,430 , GRCh38.p12 chr6: 55,653,154-55,777,632	BMP5
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	BMP5, HMGCLL1
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	BMP5, 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	BMP5, 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	BMP5, 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	BMP5, 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	BMP5, 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	BMP5, 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	BMP5, 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	BMP5, 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	BMP5, LOC442225, 104 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	BMP5, 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	BMP5, 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	BMP5, NPM1P36, 73 more genes
nsv6313741	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 55,565,835-56,277,853 , GRCh38.p12 chr6: 55,701,037-56,413,055	BMP5, LOC105375100, 4 more genes
nsv3877359	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 55,571,225-56,204,751 , GRCh38.p12 chr6: 55,706,427-56,339,953	BMP5, NPM1P36, 4 more genes
nsv6313747	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 55,731,582-56,212,819 , GRCh38.p12 chr6: 55,866,784-56,348,021	BMP5, COL21A1, 4 more genes

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