c4a[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	C4A, 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	C4A, 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	C4A, 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	C4A, 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	C4A, HLA-DPB2, 1001 more genes
nsv3913920	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028	C4A, TRR-ACG1-2, 1385 more genes
nsv4675941	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055	C4A, AGER, 217 more genes
nsv3918916	copy number variation	1	nstd102	human	Benign	NCBI36 chr6: 32,056,178-32,117,261 , GRCh37 chr6: 31,948,199-32,009,282 , GRCh38 chr6: 31,980,422-32,041,505	C4A, C4B, 6 more genes
nsv3915704	copy number variation	1	nstd102	human	Benign	NCBI36 chr6: 32,071,845-32,117,239 , GRCh37 chr6: 31,963,866-32,009,260 , GRCh38 chr6: 31,996,089-32,041,483	C4A, C4B, 5 more genes
nsv3910472	copy number variation	1	nstd102	human	Benign	NCBI36 chr6: 32,047,749-32,088,729 , GRCh37 chr6: 31,939,770-31,980,751 , GRCh38 chr6: 31,971,993-32,012,974	C4A, C4B, 5 more genes
nsv3883993	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 31,969,589-32,007,227 , GRCh38.p12 chr6: 32,001,812-32,039,450	C4A, C4B, 5 more genes
nsv3916660	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr6: 32,056,109-32,116,990 , GRCh37 chr6: 31,948,130-32,009,011 , GRCh38 chr6: 31,980,353-32,041,234	C4A, CYP21A2, 6 more genes
nsv3916509	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr6: 32,071,800-32,116,990 , GRCh37 chr6: 31,963,821-32,009,011 , GRCh38 chr6: 31,996,044-32,041,234	C4A, CYP21A2, 5 more genes
nsv3923622	copy number variation	2	nstd102	human	Likely benign	NCBI36 chr6: 32,071,800-32,116,186 , GRCh37 chr6: 31,963,821-32,008,207 , GRCh38 chr6: 31,996,044-32,040,430	C4A, TNXA, 5 more genes
nsv3921014	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr6: 32,071,800-32,115,997 , GRCh37 chr6: 31,963,821-32,008,018 , GRCh38 chr6: 31,996,044-32,040,241	C4A, TNXA, 5 more genes
nsv7097426	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 30,695,893-36,953,949 , GRCh38.p12 chr6: 30,728,116-36,986,173	C4A, LEMD2, 321 more genes
nsv3870570	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 28,130,359-32,108,367 , GRCh38.p12 chr6: 28,162,581-32,140,590	C4A, LOC105375002, 345 more genes
nsv4675453	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 31,916,915-32,278,000 , GRCh38.p12 chr6: 31,949,138-32,310,223	C4A, NOTCH4, 29 more genes
nsv3886007	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 31,952,482-32,243,155 , GRCh38.p12 chr6: 31,984,705-32,275,378	C4A, STK19B, 22 more genes

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