dbVar for Gene (Select 339983) - 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
nsv7148161	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194	SLIRPP2, STIM2-AS1, 659 more genes
nsv7148157	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396	OR7E84P, FAM193A, 764 more genes
nsv7137196	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072	ECM1P2, LOC105378240, 482 more genes
nsv7049289	inversion	1	nstd229	human		GRCh38 chr4: 1,879,237-2,966,412 , GRCh37.p13 chr4: 1,880,964-2,968,139	RNF4, SCARNA22, 28 more genes
nsv7039441	inversion	1	nstd229	human		GRCh38 chr4: 1,689,472-2,959,448 , GRCh37.p13 chr4: 1,691,199-2,961,175	NOP14-AS1, LOC112268460, 34 more genes
nsv6726652	copy number variation	1	nstd229	human		GRCh38 chr4: 2,067,576-2,071,110 , GRCh37.p13 chr4: 2,069,303-2,072,837	POLN, NAT8L
nsv6726321	copy number variation	1	nstd229	human		GRCh38 chr4: 2,059,601-2,064,600 , GRCh37.p13 chr4: 2,061,328-2,066,327	NAT8L
nsv6720202	copy number variation	1	nstd229	human		GRCh38 chr4: 2,064,630-2,064,814 , GRCh37.p13 chr4: 2,066,357-2,066,541	NAT8L
nsv6719982	copy number variation	1	nstd229	human		GRCh38 chr4: 1,983,101-2,060,400 , GRCh37.p13 chr4: 1,984,828-2,062,127	NELFA, NAT8L, 2 more genes
nsv6636691	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-2,437,290 , GRCh38.p12 chr4: 68,454-2,435,563	SPON2, TACC3, 77 more genes
nsv6636600	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 1,892,740-2,503,033 , GRCh38.p12 chr4: 1,891,013-2,501,306	LOC105374352, POLN, 19 more genes
nsv6636582	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-12,369,983 , GRCh38.p12 chr4: 68,454-12,368,359	NELFA, OR7E111FP, 289 more genes
nsv6636534	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 963,688-2,913,553 , GRCh38.p12 chr4: 969,900-2,911,826	ADD1, CTBP1, 53 more genes
nsv6636256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 1-12,785,001 , GRCh38.p12 chr4: 10,001-12,783,377	AFAP1-AS1, LOC389199, 294 more genes
nsv6634358	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344	LINC02475, LOC105374344, 658 more genes
nsv6567523	inversion	1	nstd223	human		GRCh38 chr4: 1,351,233-2,522,922 , GRCh37.p13 chr4: 1,345,021-2,524,649	LOC107986250, LOC105374348, 31 more genes
nsv6315440	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 114,784-47,569,569 , GRCh38.p12 chr4: 114,902-47,567,552	FAM86KP, ENPP7P11, 631 more genes
nsv6315365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-5,579,467 , GRCh38.p12 chr4: 68,453-5,577,740	LOC107986246, FAM53A, 149 more genes
nsv6315347	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-20,964,575 , GRCh38.p12 chr4: 68,453-20,962,952	LOC100421802, ADRA2C, 375 more genes
nsv6312255	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr4: 493,125-3,495,228 , GRCh38.p12 chr4: 499,336-3,493,501	RN7SL671P, LOC105374343, 86 more genes

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Number of Variants: 20

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Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Study Type

Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 437

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Number of Variants: 20

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