asap1[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
nsv3908894	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 131,061,531-131,062,502 , GRCh38.p12 chr8: 130,049,285-130,050,256	ASAP1
nsv3897307	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 131,370,231-131,371,106 , GRCh38.p12 chr8: 130,357,985-130,358,860	ASAP1
nsv3900108	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 131,370,559-131,371,106 , GRCh38.p12 chr8: 130,358,313-130,358,860	ASAP1
nsv3893652	copy number variation	2	nstd102	human	Benign	GRCh37 chr8: 131,359,644-131,371,106 , GRCh38.p12 chr8: 130,347,398-130,358,860	ASAP1
nsv3892768	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 131,370,231-131,377,219 , GRCh38.p12 chr8: 130,357,985-130,364,973	ASAP1
nsv6638044	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 131,108,985-131,326,757 , GRCh38.p12 chr8: 130,096,739-130,314,511	ASAP1, ASAP1-IT1
nsv3919338	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr8: 131,111,963-131,824,189 , GRCh37 chr8: 131,042,781-131,755,007 , GRCh38 chr8: 130,030,535-130,742,761	ASAP1, ASAP1-IT2, 3 more genes
nsv6637224	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133	ASAP1, RNU4-37P, 220 more genes
nsv4674996	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 126,892,814-143,750,028 , GRCh38.p12 chr8: 125,880,570-142,668,610	ASAP1, POU5F1B, 158 more genes
nsv3915490	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 127,707,788-144,459,935 , GRCh37.p13 chr8: 127,638,606-144,388,560 , GRCh38.p12 chr8: 126,626,361-143,306,390	ASAP1, LOC107986906, 179 more genes
nsv4455511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 124,120,772-135,265,846 , GRCh38.p12 chr8: 123,108,532-134,253,603	ASAP1, MTSS1, 148 more genes
nsv4457220	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 123,074,293-131,113,892 , GRCh38.p12 chr8: 122,062,054-130,101,646	ASAP1, ZHX1-C8orf76, 117 more genes
nsv3915853	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 129,176,782-134,170,188 , GRCh37 chr8: 130,189,028-135,182,431 , NCBI36 chr8: 130,258,210-135,251,613	ASAP1, RPL32P20, 52 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	ASAP1, 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	ASAP1, 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	ASAP1, 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	ASAP1, 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	ASAP1, SPAG1, 2105 more genes
nsv3908608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028	ASAP1, LINC01617, 2105 more genes
nsv3893757	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,991-146,280,828 , GRCh38.p12 chr8: 208,991-145,055,442	ASAP1, LOC105375890, 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 74

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Number of Variants: 20

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