"copy number gain"[variant_type] - 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
nsv4684021	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 135,848,568-135,891,603 , GRCh38.p12 chr2: 135,090,998-135,134,033	RAB3GAP1
nsv4684075	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr20: 18,492,869-18,496,380 , GRCh38.p12 chr20: 18,512,225-18,515,736	SEC23B
nsv3875072	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 143,500,223-149,763,815 , GRCh38.p12 chr7: 58,093,723-62,429,627	LOC101060796
nsv4350321	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 157,133,792-157,495,187 , GRCh38.p12 chr6: 156,812,658-157,174,053	ARID1B
nsv3904398	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chrX: 10,687,116-10,993,611 , GRCh37 chrX: 10,727,116-11,083,690 , GRCh38 chrX: 10,759,076-11,065,570	MID1
nsv4675164	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 69,659,882-69,912,722 , GRCh38.p12 chr7: 70,194,896-70,447,736	AUTS2
nsv3898390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 69,848,278-70,012,732 , GRCh38.p12 chr7: 70,383,292-70,547,746	AUTS2
nsv6314999	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 32,715,977-32,867,947 , GRCh38.p12 chrX: 32,697,860-32,849,830	DMD
nsv4346875	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 237,413,038-237,540,797 , GRCh38.p12 chr1: 237,249,738-237,377,497	RYR2
nsv3899148	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chrX: 32,590,404-32,687,002 , GRCh37 chrX: 32,680,483-32,777,081 , GRCh38 chrX: 32,662,366-32,758,964	DMD
nsv3908909	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 199,851,573-199,945,510 , GRCh37 chr2: 200,143,328-200,237,265 , GRCh38 chr2: 199,278,605-199,372,542	SATB2
nsv3902495	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 199,882,903-199,976,770 , GRCh37 chr2: 200,174,658-200,268,525 , GRCh38 chr2: 199,309,935-199,403,802	SATB2
nsv4685759	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 100,067,471-100,156,392 , GRCh38.p12 chr8: 99,055,243-99,144,164	VPS13B
nsv6636896	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 32,835,255-32,920,421 , GRCh38.p12 chrX: 32,817,138-32,902,304	DMD
nsv3901925	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chrX: 31,446,998-31,529,862 , GRCh37 chrX: 31,537,077-31,619,941 , GRCh38 chrX: 31,518,960-31,601,824	DMD
nsv3915273	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 46,515,527-46,581,095 , GRCh37 chr15: 48,728,235-48,793,803 , GRCh38 chr15: 48,436,038-48,501,606	FBN1
nsv3881877	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 149,201,266-149,239,392 , GRCh38.p12 chr2: 148,443,697-148,481,823	MBD5
nsv4685581	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chrX: 585,079-619,564 , GRCh38.p12 chrX: 624,344-658,829	SHOX
nsv3894585	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chrX: 110,448,204-110,478,062 , GRCh37 chrX: 110,561,548-110,591,406 , GRCh38 chrX: 111,318,320-111,348,178	DCX
nsv3920315	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 149,728,077-149,756,599 , GRCh37 chr5: 149,747,884-149,776,406 , GRCh38 chr5: 150,368,321-150,396,843	TCOF1

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Items: 1 to 20 of 274538

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Number of Variants: 20

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