abra[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
nsv3896594	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 107,779,580-107,819,358 , GRCh38.p12 chr8: 106,767,352-106,807,130	ABRA
nsv3896084	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 107,807,716-107,839,322 , GRCh38.p12 chr8: 106,795,488-106,827,094	ABRA
nsv3921895	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 107,773,356-107,796,490 , GRCh38 chr8: 106,761,128-106,784,262 , NCBI36 chr8: 107,842,532-107,865,666	ABRA
nsv3921203	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr8: 107,796,490-108,393,008 , NCBI36 chr8: 107,865,666-108,462,184 , GRCh38 chr8: 106,784,262-107,380,780	ABRA, LOC105375701, 2 more genes
nsv3898331	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 107,807,716-108,389,187 , GRCh38.p12 chr8: 106,795,488-107,376,959	ABRA, ANGPT1, 2 more genes
nsv3901430	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr8: 107,819,033-108,392,816 , GRCh38.p12 chr8: 106,806,805-107,380,588	ABRA, LOC105375701, 2 more genes
nsv3908577	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 107,509,850-107,773,415 , GRCh38.p12 chr8: 106,497,622-106,761,187	ABRA, TAGLN2P1, 3 more genes
nsv3902331	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 107,817,356-108,392,816 , GRCh38.p12 chr8: 106,805,128-107,380,588	ABRA, ANGPT1, 2 more genes
nsv3917227	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 107,817,356-108,392,282 , GRCh38 chr8: 106,805,128-107,380,054 , NCBI36 chr8: 107,886,532-108,461,458	ABRA, HMGB1P46, 2 more genes
nsv3918900	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 107,796,490-108,368,465 , GRCh38 chr8: 106,784,262-107,356,237 , NCBI36 chr8: 107,865,666-108,437,641	ABRA, LOC105375701, 2 more genes
nsv3911631	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 107,813,722-108,338,822 , GRCh38 chr8: 106,801,494-107,326,594 , NCBI36 chr8: 107,882,898-108,407,998	ABRA, LOC105375701, 2 more genes
nsv3901450	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 107,032,887-120,742,018 , GRCh38.p12 chr8: 106,020,659-119,729,778	ABRA, AARD, 112 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	ABRA, HMGB1P46, 109 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	ABRA, BAALC-AS1, 79 more genes
nsv3914089	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 106,065,758-108,815,763 , GRCh38 chr8: 105,053,530-107,803,535 , NCBI36 chr8: 106,134,934-108,884,939	ABRA, ANGPT1, 16 more genes
nsv3915173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636	ABRA, RN7SL474P, 2109 more genes
nsv3901821	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028	ABRA, TBC1D31, 2109 more genes
nsv4349554	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385	ABRA, LOC101929488, 2105 more genes
nsv3916777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575	ABRA, RPL5P22, 2105 more genes
nsv3898123	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385	ABRA, SPAG1, 2105 more genes

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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 50

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Number of Variants: 20

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