dbVar for Gene (Select 102466865) - 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
nsv7148238	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378	CCDC26, EFR3A, 238 more genes
nsv7148132	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 131,138,343-143,473,913 , GRCh38.p12 chr8: 130,126,097-142,392,552	LOC107983985, MIR30DHG, 104 more genes
nsv6844385	copy number variation	1	nstd229	human		GRCh38 chr8: 132,809,731-133,525,064 , GRCh37.p13 chr8: 133,821,976-134,537,307	CCN4, ST13P6, 14 more genes
nsv6841401	copy number variation	1	nstd229	human		GRCh38 chr8: 133,010,316-136,879,429 , GRCh37.p13 chr8: 134,022,561-137,891,672	LOC107986978, LOC101927822, 35 more genes
nsv6634360	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385	WASHC5, LOC100132280, 1028 more genes
nsv6432116	copy number variation	1	nstd223	human		GRCh38 chr8: 133,026,354-133,228,293 , GRCh37.p13 chr8: 134,038,599-134,240,536	PTCSC1, LOC105375769, 5 more genes
nsv6315406	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385	RHPN1, RPL18P7, 833 more genes
nsv6314744	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325	OSR2, LOC392268, 676 more genes
nsv6313759	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385	LOC101927066, NCAPGP1, 1014 more genes
nsv6313487	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 130,863,093-146,295,771 , GRCh38.p12 chr8: 129,850,847-145,070,385	LOC105375784, CYP11B2, 253 more genes
nsv6290242	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 128,878,931-141,662,233 , GRCh38.p12 chr8: 127,866,685-140,652,134	LINC02055, LOC101927798, 100 more genes
nsv6136327	copy number variation	1	nstd213	human		GRCh37 chr8: 134,010,000-134,540,001 , GRCh38.p12 chr8: 132,997,755-133,527,758	MIR7848, ST3GAL1, 13 more genes
nsv6136325	copy number variation	1	nstd213	human		GRCh37 chr8: 133,500,000-134,270,001 , GRCh38.p12 chr8: 132,487,753-133,257,758	NDRG1, HPYR1, 14 more genes
nsv6136318	copy number variation	1	nstd213	human		GRCh37 chr8: 128,550,000-134,990,001 , GRCh38.p12 chr8: 127,537,755-133,977,758	CCN4, PHF20L1, 67 more genes
nsv6136082	copy number variation	1	nstd213	human		GRCh37 chr8: 86,730,000-142,740,001 , GRCh38.p12 chr8: 85,717,771-141,729,803	ANXA13, ATP6V1C1, 658 more genes
nsv6136003	copy number variation	1	nstd213	human		GRCh37 chr8: 133,920,000-137,040,001 , GRCh38.p12 chr8: 132,907,755-136,027,758	SLA, RPL32P20, 33 more genes
nsv6135831	copy number variation	1	nstd213	human		GRCh37 chr8: 133,820,000-134,290,001 , GRCh38.p12 chr8: 132,807,755-133,277,758	TG, CCN4, 9 more genes
nsv5673945	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr8: 133,141,509-134,296,554 , GRCh38.p12 chr8: 132,129,262-133,284,311	SLA, TMEM71, 15 more genes
nsv4675664	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 128,877,995-146,295,771 , GRCh38.p12 chr8: 127,865,749-145,070,385	LOC105375789, LINC02990, 270 more genes
nsv4675273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385	TOP1MT, SLA, 379 more genes

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 169

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Number of Variants: 20

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