dbVar for Gene (Select 117166) - 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
nsv6976504	copy number variation	1	nstd229	human		GRCh38 chr16: 599,402-638,384 , GRCh37.p13 chr16: 649,402-688,384	TRG-CCC2-2, RAB40C, 3 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
nsv6968024	copy number variation	1	nstd229	human		GRCh38 chr16: 631,153-633,052 , GRCh37.p13 chr16: 681,153-683,052	WFIKKN1, METTL26
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
nsv6623481	copy number variation	2	nstd224	human		GRCh37 chr16: 640,329-683,959 , GRCh38.p12 chr16: 590,329-633,959	RAB40C, METTL26, 1 more genes
nsv6623477	copy number variation	1	nstd224	human		GRCh37 chr16: 633,125-683,399 , GRCh38.p12 chr16: 583,125-633,399	RAB40C, METTL26, 2 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
nsv6511799	copy number variation	1	nstd223	human		GRCh38 chr16: 631,152-633,050 , GRCh37.p13 chr16: 681,152-683,050	WFIKKN1, METTL26
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
nsv6203613	copy number variation	1	nstd214	human		GRCh38 chr16: 631,744-631,828 , GRCh37.p13 chr16: 681,744-681,828	WFIKKN1
nsv6202103	copy number variation	1	nstd214	human		GRCh38 chr16: 632,022-632,109 , GRCh37.p13 chr16: 682,022-682,109	WFIKKN1
nsv6195086	copy number variation	1	nstd214	human		GRCh38 chr16: 631,727-631,886 , GRCh37.p13 chr16: 681,727-681,886	WFIKKN1

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Number of Variants: 20

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 520

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Number of Variants: 20

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