st7[All Fields] AND 1[has_clinical] - 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
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	ST7, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	ST7, LOC107986817, 2014 more genes
nsv3924380	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 101,912,320-120,918,695 , GRCh38 chr7: 102,196,924-121,278,641 , NCBI36 chr7: 101,626,924-120,705,931	ST7, LOC102724434, 222 more genes
nsv6313576	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106	ST7, LHFPL3-AS2, 233 more genes
nsv4675322	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 106,617,406-123,217,914 , GRCh38.p12 chr7: 106,976,961-123,577,860	ST7, CBLL1-AS1, 168 more genes
nsv3900620	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 111,613,396-127,897,316 , GRCh38.p12 chr7: 111,973,341-128,257,263	ST7, LSM8, 170 more genes
nsv3923570	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 107,583,881-122,963,817 , GRCh37.p13 chr7: 107,796,645-123,176,581 , GRCh38.p12 chr7: 108,156,200-123,536,527	ST7, ANKRD7, 142 more genes
nsv3916529	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 113,782,532-125,480,435 , NCBI36 chr7: 113,569,768-125,267,671 , GRCh38 chr7: 114,142,477-125,840,381	ST7, CAPZA2, 124 more genes
nsv3922792	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 113,227,126-124,326,508 , GRCh37 chr7: 113,439,890-124,539,272 , GRCh38 chr7: 113,799,835-124,899,218	ST7, MTND4P6, 116 more genes
nsv4455557	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,410,314-117,825,549 , GRCh38.p12 chr7: 107,769,869-118,185,495	ST7, RAC1P6, 103 more genes
nsv5381759	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 116,297,277-126,370,694 , GRCh38.p12 chr7: 116,657,223-126,730,640	ST7, TMEM229A, 110 more genes
nsv3882930	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 111,781,517-120,142,536 , GRCh37.p13 chr7: 111,994,281-120,355,300 , GRCh38.p12 chr7: 112,354,226-120,715,246	ST7, LOC105375472, 78 more genes
nsv3922470	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 102,183,491-110,139,893 , GRCh38 chr8: 101,171,263-109,127,664 , NCBI36 chr8: 102,252,667-110,209,069	HMGB1P46, RPS12P15, 109 more genes
nsv3913241	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 101,260,812-107,606,071 , GRCh38 chr8: 100,179,408-106,524,667 , GRCh37 chr8: 101,191,636-107,536,895	LRP12, PTMAP15, 113 more genes
nsv3919996	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 102,897,047-108,368,371 , GRCh38 chr8: 101,884,819-107,356,143 , NCBI36 chr8: 102,966,223-108,437,547	BAALC-AS1, AZIN1, 79 more genes
nsv3910618	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 102,281,230-106,883,502 , GRCh38 chr8: 101,199,826-105,802,098 , GRCh37 chr8: 102,212,054-106,814,326	LINC03047, LOC100419977, 84 more genes
nsv3912650	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 114,538,937-117,430,177 , GRCh38 chr7: 114,898,882-117,790,123 , NCBI36 chr7: 114,326,173-117,217,413	ST7, LOC100421782, 40 more genes
nsv3911722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 114,029,450-116,893,795 , GRCh38 chr7: 114,389,395-117,253,741 , NCBI36 chr7: 113,816,686-116,681,031	ST7, TFEC, 31 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	ST7, RNU6-565P, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	ST7, RPL23AP51, 2684 more genes

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Number of Variants: 20

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dbVar

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

Search results

Items: 1 to 20 of 80

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Number of Variants: 20

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Supplemental Content

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Search details

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