dbVar for Gene (Select 92070) - 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
nsv7097251	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 493,125-1,843,544 , GRCh38.p12 chr4: 499,336-1,841,817	PDE6B, LOC105374339, 44 more genes
nsv6737250	copy number variation	1	nstd229	human		GRCh38 chr4: 1,239,705-1,265,646 , GRCh37.p13 chr4: 1,233,493-1,259,434	CTBP1, CTBP1-DT
nsv6728098	copy number variation	1	nstd229	human		GRCh38 chr4: 1,245,554-1,247,764 , GRCh37.p13 chr4: 1,239,342-1,241,552	CTBP1-DT, CTBP1
nsv6718854	copy number variation	1	nstd229	human		GRCh38 chr4: 1,245,501-1,249,100 , GRCh37.p13 chr4: 1,239,289-1,242,888	CTBP1, CTBP1-DT
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
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
nsv6636307	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 1,180,181-2,009,278 , GRCh38.p12 chr4: 1,186,393-2,007,551	LOC105374348, SPON2, 22 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
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
nsv6315414	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 68,345-1,512,353 , GRCh38.p12 chr4: 68,453-1,510,626	ATP5ME, CTBP1, 50 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
nsv6315218	complex substitution	1	nstd102	human	Pathogenic	GRCh38.p12 chr4: 68,453-1,868,821 , GRCh37 chr4: 68,345-1,870,548	ATP5ME, CTBP1, 59 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
nsv6311726	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 493,125-2,065,854 , GRCh38.p12 chr4: 499,336-2,064,127	SLC49A3, LOC105374348, 51 more genes

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 411

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Number of Variants: 20

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