dbVar for Gene (Select 57799) - 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
nsv6974857	copy number variation	1	nstd229	human		GRCh38 chr16: 394,003-596,867 , GRCh37.p13 chr16: 444,003-646,867	CAPN15, MIR5587, 9 more genes
nsv6974504	copy number variation	1	nstd229	human		GRCh38 chr16: 581,493-589,241 , GRCh37.p13 chr16: 631,493-639,241	PIGQ, RAB40C
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
nsv6973009	copy number variation	1	nstd229	human		GRCh38 chr16: 584,489-589,099 , GRCh37.p13 chr16: 634,489-639,099	RAB40C, PIGQ
nsv6972907	copy number variation	1	nstd229	human		GRCh38 chr16: 585,399-618,637 , GRCh37.p13 chr16: 635,399-668,637	RAB40C
nsv6970436	copy number variation	1	nstd229	human		GRCh38 chr16: 528,697-616,825 , GRCh37.p13 chr16: 578,697-666,825	RAB40C, MIR5587, 5 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
nsv6964525	copy number variation	1	nstd229	human		GRCh38 chr16: 581,517-589,519 , GRCh37.p13 chr16: 631,517-639,519	PIGQ, RAB40C
nsv6964230	copy number variation	1	nstd229	human		GRCh38 chr16: 594,314-601,402 , GRCh37.p13 chr16: 644,314-651,402	RAB40C
nsv6962113	copy number variation	1	nstd229	human		GRCh38 chr16: 620,338-620,374 , GRCh37.p13 chr16: 670,338-670,374	RAB40C
nsv6960310	copy number variation	1	nstd229	human		GRCh38 chr16: 615,400-615,438 , GRCh37.p13 chr16: 665,400-665,438	RAB40C
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

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Number of Variants: 20

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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

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Items: 1 to 20 of 721

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Number of Variants: 20

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