dbVar for Gene (Select 105371038) - 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
nsv7094666	copy number variation	3	nstd102	human	Uncertain significance	GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571	DNAAF8, TMEM204, 282 more genes
nsv7094665	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 256,302-1,918,176 , GRCh38.p12 chr16: 206,303-1,868,175	MRPS34, LOC105371044, 97 more genes
nsv7094664	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 256,302-1,843,653 , GRCh38.p12 chr16: 206,303-1,793,652	NME4, UNKL, 94 more genes
nsv7094663	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 256,302-1,657,267 , GRCh38.p12 chr16: 206,303-1,607,266	TPSP2, PRR25, 83 more genes
nsv7064153	inversion	1	nstd229	human		GRCh38 chr16: 463,012-758,884 , GRCh37.p13 chr16: 513,012-808,884	LINC00235, ANTKMT, 27 more genes
nsv6973281	copy number variation	1	nstd229	human		GRCh38 chr16: 622,106-656,922 , GRCh37.p13 chr16: 672,106-706,922	METTL26, LOC105371038, 6 more genes
nsv6966485	copy number variation	1	nstd229	human		GRCh38 chr16: 539,563-712,009 , GRCh37.p13 chr16: 589,563-762,009	RHBDL1, PIGQ, 18 more genes
nsv6958605	copy number variation	1	nstd229	human		GRCh38 chr16: 628,893-653,888 , GRCh37.p13 chr16: 678,893-703,888	METTL26, LOC105371038, 6 more genes
nsv6637972	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-1,350,186 , GRCh38.p12 chr16: 35,881-1,300,185	MPG, LOC105371038, 78 more genes
nsv6634427	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458	HBA1, ANTKMT, 312 more genes
nsv6515368	copy number variation	1	nstd223	human		GRCh38 chr16: 622,106-656,924 , GRCh37.p13 chr16: 672,106-706,924	TRG-CCC2-2, METTL26, 6 more genes
nsv6314105	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-1,468,828 , GRCh38.p12 chr16: 35,880-1,418,827	HBA2, LUC7L, 87 more genes
nsv6133278	copy number variation	2	nstd213	human		GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144	, ABAT, 446 more genes
nsv6112797	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012	ANTKMT, HBA1, 307 more genes
nsv5514700	copy number variation	1	nstd206	human		GRCh38 chr16: 646,729-647,194 , GRCh37.p13 chr16: 696,729-697,194	LOC105371038, MCRIP2
nsv5380998	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr16: 624,055-2,153,916 , GRCh38.p12 chr16: 574,055-2,103,915	NDUFB10, BAIAP3, 102 more genes
nsv5279314	copy number variation	1	nstd204	human		GRCh38.p13 chr16: 631,501-737,100 , GRCh37.p13 chr16: 681,501-787,100	, CIAO3, 18 more genes
nsv5278593	copy number variation	1	nstd204	human		GRCh38.p13 chr16: 495,101-1,599,500 , GRCh37.p13 chr16: 545,101-1,649,501	, MIR662, 73 more genes
nsv5265522	copy number variation	1	nstd204	human		GRCh38.p13 chr16: 53,201-2,576,200 , GRCh37.p13 chr16: 103,201-2,626,201	, RHBDL1, 175 more genes
nsv5263615	copy number variation	1	nstd204	human		GRCh38.p13 chr16: 504,601-857,400 , GRCh37.p13 chr16: 554,601-907,400	, LINC00235, 36 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Links from Gene

Items: 1 to 20 of 493

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Number of Variants: 20

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