clic5[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
nsv3881843	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 45,951,349-46,067,273 , GRCh38.p12 chr6: 45,983,612-46,099,536	CLIC5, RNU6-754P
nsv5673768	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 45,296,464-46,047,979 , GRCh38.p12 chr6: 45,328,727-46,080,242	CLIC5, SUPT3H, 3 more genes
nsv3920961	copy number variation	1	nstd102	human	not provided	NCBI36 chr6: 45,579,286-46,089,921 , GRCh37.p13 chr6: 45,471,308-45,981,962 , GRCh38.p12 chr6: 45,503,571-46,014,225	CLIC5, RUNX2, 1 more genes
nsv3911674	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 45,475,088-45,982,640 , NCBI36 chr6: 45,583,066-46,090,599 , GRCh38 chr6: 45,507,351-46,014,903	CLIC5, RUNX2, 1 more genes
nsv3923721	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 45,681,671-54,212,044 , GRCh37 chr6: 45,649,408-54,076,842 , NCBI36 chr6: 45,757,386-54,184,801	CLIC5, PAQR8, 131 more genes
nsv3884243	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 43,636,308-50,947,320 , GRCh38.p12 chr6: 43,668,571-50,979,607	CLIC5, GLYATL3, 105 more genes
nsv3912856	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 41,713,777-46,588,645 , GRCh38 chr6: 41,638,061-46,512,949 , GRCh37 chr6: 41,605,799-46,480,686	CLIC5, PTCRA, 121 more genes
nsv3919402	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 42,769,519-46,417,784 , GRCh37.p13 chr6: 42,661,541-46,309,825 , GRCh38.p12 chr6: 42,693,803-46,342,088	CLIC5, LOC101929770, 94 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	CLIC5, 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	CLIC5, 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	CLIC5, 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	CLIC5, 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	CLIC5, 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	CLIC5, TRR-ACG1-2, 1385 more genes
nsv6290720	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38.p12 chr6: 45,316,919-46,189,287 , GRCh37 chr6: 45,284,656-46,157,024	CLIC5, RUNX2, 5 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	CLIC5, ACTG1P9, 245 more genes
nsv3919465	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr6: 45,061,475-48,062,533 , GRCh37 chr6: 44,953,497-47,954,574 , GRCh38 chr6: 44,985,760-47,986,838	CLIC5, ACTG1P9, 40 more genes
nsv3921428	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 44,961,189-46,029,602 , GRCh38 chr6: 44,993,452-46,061,865 , NCBI36 chr6: 45,069,167-46,137,561	CLIC5, RUNX2, 6 more genes
nsv3874694	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 45,061,951-45,871,043 , GRCh38.p12 chr6: 45,094,214-45,903,306	CLIC5, SUPT3H, 5 more genes

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