zmym4[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
nsv4346788	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 32,859,415-36,454,915 , GRCh38.p12 chr1: 32,393,814-35,989,314	ZMYM4, LOC100419802, 75 more genes
nsv6636592	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 35,104,233-37,357,913 , GRCh38.p12 chr1: 34,638,632-36,892,312	ZMYM4, EFCAB14P1, 56 more genes
nsv3883608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 34,830,287-36,945,093 , GRCh38.p12 chr1: 34,364,686-36,479,492	ZMYM4, LSM10, 52 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	ZMYM4, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	ZMYM4, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	ZMYM4, RNU1-153P, 4887 more genes
nsv3901163	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 24,707,696-41,886,350 , GRCh38 chr1: 24,381,206-41,401,517 , NCBI36 chr1: 24,580,283-41,658,937	ZMYM4, TMEM222, 453 more genes
nsv6313688	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139	ZMYM4, LOC107984940, 407 more genes
nsv3874782	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 31,562,164-37,421,958 , GRCh38.p12 chr1: 31,089,317-36,956,357	ZMYM4, LOC101929444, 143 more genes
nsv3890386	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr1: 34,992,126-36,293,498 , GRCh37 chr1: 35,219,539-36,520,911 , GRCh38 chr1: 34,753,938-36,055,310	ZMYM4, GJA4, 31 more genes
nsv4578482	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 35,321,300-35,944,813 , GRCh38.p12 chr1: 34,855,699-35,479,212	ZMYM4, LOC105378644, 14 more genes
nsv4436181	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532	ZMYM4, LINC01776, 1853 more genes
nsv3878135	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 33,241,563-46,663,513 , GRCh38.p12 chr1: 32,775,962-46,197,841	ZMYM4, LINC02786, 365 more genes
nsv4450314	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 34,915,050-36,163,162 , GRCh38.p12 chr1: 34,449,449-35,697,561	ZMYM4, LOC105378644, 27 more genes

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zmym4[All Fields] AND 1[has_clinical] (15)
dbVar
RecName: Full=ATP-sensitive inward rectifier potassium channel 8; AltName: Full=...
RecName: Full=ATP-sensitive inward rectifier potassium channel 8; AltName: Full=Inward rectifier K(+) channel Kir6.1; AltName: Full=Potassium channel, inwardly rectifying subfamily J member 8; AltName: Full=uKATP-1
gi|2493602|sp|Q63664.1|KCNJ8_RAT

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