dbVar for Gene (Select 2971) - 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
nsv6933838	copy number variation	1	nstd229	human		GRCh38 chr13: 27,426,427-27,426,454 , GRCh37.p13 chr13: 28,000,564-28,000,591	GTF3A
nsv6930563	copy number variation	1	nstd229	human		GRCh38 chr13: 27,129,201-27,579,100 , GRCh37.p13 chr13: 27,703,338-28,153,237	MTIF3, USP12-AS1, 14 more genes
nsv6927821	copy number variation	1	nstd229	human		GRCh38 chr13: 27,434,985-27,468,996 , GRCh37.p13 chr13: 28,009,122-28,043,133	GTF3A, MTIF3
nsv6924800	copy number variation	1	nstd229	human		GRCh38 chr13: 27,209,622-27,517,803 , GRCh37.p13 chr13: 27,783,759-28,091,940	SNORD102, MTIF3, 10 more genes
nsv6923289	copy number variation	1	nstd229	human		GRCh38 chr13: 27,430,642-27,443,274 , GRCh37.p13 chr13: 28,004,779-28,017,411	GTF3A, MTIF3
nsv6922691	copy number variation	1	nstd229	human		GRCh38 chr13: 27,424,001-27,425,100 , GRCh37.p13 chr13: 27,998,138-27,999,237	GTF3A
nsv6922461	copy number variation	1	nstd229	human		GRCh38 chr13: 27,337,201-27,491,900 , GRCh37.p13 chr13: 27,911,338-28,066,037	MTIF3, RNY1P1, 4 more genes
nsv6920474	copy number variation	1	nstd229	human		GRCh38 chr13: 27,261,701-27,553,400 , GRCh37.p13 chr13: 27,835,838-28,127,537	RNY1P1, MTIF3, 6 more genes
nsv6918151	copy number variation	1	nstd229	human		GRCh38 chr13: 27,165,601-27,598,600 , GRCh37.p13 chr13: 27,739,738-28,172,737	RASL11A, LOC105370126, 14 more genes
nsv6634431	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462	MTUS2-AS1, LOC105370213, 1330 more genes
nsv6484667	copy number variation	1	nstd223	human		GRCh38 chr13: 27,209,622-27,517,805 , GRCh37.p13 chr13: 27,783,759-28,091,942	MTIF3, LOC105370126, 10 more genes
nsv6315495	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403	RNU6-80P, EFNB2, 1334 more genes
nsv6314030	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251	RPSAP53, LOC105370213, 1310 more genes
nsv6289999	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403	LINC00363, LOC105370118, 1334 more genes
nsv6132752	copy number variation	1	nstd213	human		GRCh37 chr13: 27,480,000-28,970,001 , GRCh38.p12 chr13: 26,905,863-28,395,864	CDX2, FLT1, 41 more genes
nsv6132543	copy number variation	1	nstd213	human		GRCh37 chr13: 19,020,000-67,280,001 , GRCh38.p12 chr13: 18,445,862-66,705,869	, PARP4, 770 more genes
nsv6132475	copy number variation	1	nstd213	human		GRCh37 chr13: 26,620,000-32,650,001 , GRCh38.p12 chr13: 26,045,862-32,075,864	ALOX5AP, HMGB1, 106 more genes
nsv5564510	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053	RN7SL272P, DIAPH3, 1333 more genes
nsv5494963	copy number variation	1	nstd206	human		GRCh38 chr13: 27,424,032-27,424,095 , GRCh37.p13 chr13: 27,998,169-27,998,232	GTF3A
nsv5319647	copy number variation	1	nstd204	human		GRCh38.p13 chr13: 27,401,280-27,501,044 , GRCh37.p13 chr13: 27,975,417-28,075,181	MTIF3, RNY1P1, 2 more genes

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Number of Variants: 20

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Items: 1 to 20 of 126

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Number of Variants: 20

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