atp6v1g2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 13

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Number of Variants: 13

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	ATP6V1G2, 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	ATP6V1G2, 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	ATP6V1G2, 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	ATP6V1G2, 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	ATP6V1G2, 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	ATP6V1G2, TRR-ACG1-2, 1385 more genes
nsv6289880	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 28,005,012-31,683,185 , GRCh38.p12 chr6: 28,037,234-31,715,408	ATP6V1G2, ABCF1, 313 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	ATP6V1G2, AGER, 217 more genes
nsv3914743	copy number variation	1	nstd102	human	Benign	NCBI36 chr6: 31,344,150-31,633,186 , GRCh37.p13 chr6\|NT_167249.1: 2,583,945-2,755,239 , GRCh37.p13 chr6\|NT_167246.1: 2,583,066-2,868,097 , GRCh37.p13 chr6: 31,236,171-31,525,207 , GRCh38.p12 chr6: 31,268,394-31,557,430 , GRCh38.p12 chr6\|NT_167249.2: 2,584,647-2,755,941 , GRCh38.p12 chr6\|NT_167246.2: 2,577,446-2,862,477	ATP6V1G2, LINC01149, 30 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	ATP6V1G2, 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	ATP6V1G2, LOC105375002, 345 more genes
nsv7097325	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 30,695,893-31,937,492 , GRCh38.p12 chr6: 30,728,116-31,969,715	ATP6V1G2, HCG21, 117 more genes
nsv3876127	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 31,384,577-31,902,308 , GRCh38.p12 chr6: 31,416,800-31,934,531	ATP6V1G2, HCP5, 66 more genes

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