vps52[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 12

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	VPS52, 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	VPS52, 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	VPS52, 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	VPS52, 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	VPS52, 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	VPS52, 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	VPS52, AGER, 217 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	VPS52, LEMD2, 321 more genes
nsv7098787	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 32,148,920-36,953,949 , GRCh38.p12 chr6: 32,181,143-36,986,173	VPS52, CUTA, 184 more genes
nsv6313582	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 33,069,892-33,751,391 , GRCh38.p12 chr6: 33,102,115-33,783,614	VPS52, LOC107986537, 46 more genes
nsv4451881	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 33,131,435-33,419,703 , GRCh38 chr6: 33,163,658-33,451,926	VPS52, COL11A2, 29 more genes
nsv4682849	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 33,141,458-33,419,703 , GRCh38.p12 chr6: 33,173,681-33,451,926	VPS52, RPL35AP4, 29 more genes

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