dbVar for Gene (Select 54981) - 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
nsv5715270	mobile element insertion	1	nstd211	human		GRCh38 chr9: 75,077,381-75,077,381 , GRCh37.p13 chr9: 77,692,297-77,692,297	NMRK1
nsv5372600	translocation	1	nstd200	human		GRCh38 chr9: 75,077,084-75,077,084 , GRCh38 chr9: 75,077,290-75,077,290 , GRCh37.p13 chr9: 77,692,206-77,692,206 , GRCh37.p13 chr9: 77,692,000-77,692,000	NMRK1
nsv5132558	mobile element insertion	1	nstd203	human		GRCh38 chr9: 75,074,433-75,074,433 , GRCh37.p13 chr9: 77,689,349-77,689,349	NMRK1
nsv4570283	mobile element insertion	1	nstd166	human		GRCh37.p13 chr9: 77,683,347-77,683,347 , GRCh38.p12 chr9: 75,068,431-75,068,431	NMRK1
nsv4457273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936	CDRT15P14, MIR548AW, 2167 more genes
nsv4455928	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 70,974,661-81,829,792 , GRCh38.p12 chr9: 68,359,745-79,214,877	RPL35AP21, LOC105376097, 134 more genes
nsv4455186	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937	LOC105376327, ENG, 1304 more genes
nsv4436161	complex substitution	1	nstd102	human	Likely pathogenic	GRCh38.p12 chr9: 23,524,428-84,744,973 , GRCh37 chr9: 23,524,426-87,359,888	ACO1, ALDH1A1, 779 more genes
nsv3923526	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 74,029,084-79,136,863 , GRCh37 chr9: 74,839,264-79,947,043 , GRCh38 chr9: 72,224,348-77,332,127	GCNT1, NMRK1, 65 more genes
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	TDRD7, CDK9, 2170 more genes
nsv3921710	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr9: 74,282,586-75,968,293 , GRCh37 chr9: 76,897,502-78,583,209 , NCBI36 chr9: 76,087,322-77,773,029	RNU6-1228P, NMRK1, 20 more genes
nsv3921598	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389	PGAP4, ECPAS, 2167 more genes
nsv3921099	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr9: 76,692,722-77,522,931 , GRCh37 chr9: 77,502,902-78,333,111 , GRCh38 chr9: 74,887,986-75,718,195	NMRK1, TRPM6, 8 more genes
nsv3920777	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 70,259,583-78,057,599 , GRCh38 chr9: 68,454,847-76,252,863 , GRCh37 chr9: 71,130,848-78,867,779	ANXA1, LOC105376080, 96 more genes
nsv3920713	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389	ABHD17B, LOC100533707, 2167 more genes
nsv3919257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718	LOC107987031, LOC105376234, 2169 more genes
nsv3917022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 214,367-141,008,915 , GRCh38 chr9: 193,412-138,114,463 , NCBI36 chr9: 204,367-140,128,736	RN7SKP87, SPATA6L, 2168 more genes
nsv3915973	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,159,073 , GRCh37 chr9: 68,420,641-141,053,525 , NCBI36 chr9: 67,910,461-140,173,346	CTNNAL1, QSOX2, 2170 more genes
nsv3915174	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 70,304,266-85,474,962 , GRCh38 chr9: 68,499,530-83,670,227 , GRCh37 chr9: 71,130,848-86,285,142	LOC107987086, PGM5, 183 more genes
nsv3914702	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 71,130,848-109,341,774 , NCBI36 chr9: 70,225,166-108,381,595 , GRCh38 chr9: 68,420,430-106,579,493	CDCA7P2, ASPN, 603 more genes

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Number of Variants: 20

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