znf184[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3879184	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 27,318,836-27,329,267 , GRCh38.p12 chr6: 27,351,057-27,361,488	ZNF204P
nsv3884649	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr6: 27,327,688-27,369,166 , GRCh38.p12 chr6: 27,359,909-27,401,387	ZNF391, ZNF204P
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	ZNF184, 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	ZNF184, 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	ZNF184, 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	ZNF184, ITPR3, 2905 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	ZNF184, TRR-ACG1-2, 1385 more genes
nsv3920564	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946	ZNF184, PRELID1P2, 785 more genes
nsv3883304	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 27,433,995-27,471,515 , GRCh38.p12 chr6: 27,466,216-27,503,736	ZNF184, TRS-AGA2-3, 5 more genes
nsv3885517	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 27,431,828-27,489,398 , GRCh38.p12 chr6: 27,464,049-27,521,619	ZNF184, HNRNPA1P1, 8 more genes
nsv4456157	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 27,209,501-27,432,468 , GRCh38.p12 chr6: 27,241,722-27,464,689	ZNF184, TRI-AAT9-1, 17 more genes
nsv3911053	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr6: 26,280,579-28,727,313 , GRCh37 chr6: 26,280,807-28,695,090 , NCBI36 chr6: 26,388,786-28,803,069	ZNF184, GPX5, 232 more genes
nsv3873727	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 26,928,203-27,344,831 , GRCh38.p12 chr6: 26,960,424-27,377,052	TRV-CAC6-1, CDCA7P1, 42 more genes
nsv3886559	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 27,166,564-27,432,468 , GRCh38.p12 chr6: 27,198,785-27,464,689	ZNF184, ZNF204P, 25 more genes

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