kcnq5[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7097083	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 73,713,611-73,713,741 , GRCh38.p12 chr6: 73,003,888-73,004,018	KCNQ5
nsv4676043	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 73,364,326-73,721,064 , GRCh38.p12 chr6: 72,654,598-73,011,341	KCNQ5, KNOP1P4, 3 more genes
nsv3924180	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 65,316,269-84,193,229 , GRCh38 chr6: 64,549,655-83,426,791 , GRCh37 chr6: 65,259,548-84,136,510	KCNQ5, LOC105377875, 188 more genes
nsv6315402	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 64,954,687-79,581,678 , GRCh38.p12 chr6: 64,244,794-78,871,961	KCNQ5, LOC105377841, 139 more genes
nsv3889959	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 73,674,612-84,829,774 , GRCh38.p12 chr6: 72,964,889-84,120,055	KCNQ5, MRAP2, 125 more genes
nsv6291322	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 72,799,054-83,275,894 , GRCh38.p12 chr6: 72,089,351-82,566,177	KCNQ5, RPS27P15, 118 more genes
nsv6291339	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 70,165,296-79,920,769 , GRCh38.p12 chr6: 69,455,404-79,211,052	KCNQ5, RNU6-84P, 113 more genes
nsv6634377	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 71,105,038-75,200,617 , GRCh38.p12 chr6: 70,395,335-74,490,901	KCNQ5, TXNP7, 63 more genes
nsv5673923	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 72,596,727-74,363,609 , GRCh38.p12 chr6: 71,887,024-73,653,886	KCNQ5, LOC100422453, 32 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	KCNQ5, 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	KCNQ5, 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	KCNQ5, 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	KCNQ5, 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	KCNQ5, HLA-DPB2, 1001 more genes
nsv6313857	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492	KCNQ5, LOC101928570, 288 more genes
nsv6637121	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 72,886,775-73,507,843 , GRCh38.p12 chr6: 72,177,072-72,798,120	KCNQ5, LOC643067, 6 more genes
nsv7097082	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 72,889,258-73,332,335 , GRCh38.p12 chr6: 72,179,555-72,622,607	KCNQ5, LOC643067, 5 more genes
nsv3911444	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 73,697,858-73,935,015 , GRCh38 chr6: 72,988,135-73,225,292	KCNQ5, KNOP1P4, 5 more genes
nsv6312591	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 73,879,449-74,210,458 , GRCh38.p12 chr6: 73,169,726-73,500,735	KCNQ5, DPPA5, 16 more genes
nsv4675253	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 73,881,985-74,138,519 , GRCh38.p12 chr6: 73,172,262-73,428,796	KCNQ5, OOEP, 13 more genes

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Items: 20

Number of Variants: 20

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