dnaaf11[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
nsv5673946	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr8: 133,584,534-133,584,748 , GRCh38.p12 chr8: 132,572,286-132,572,500	DNAAF11
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	DNAAF11, 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	DNAAF11, 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	DNAAF11, 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	DNAAF11, MTSS1, 148 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	DNAAF11, RPL32P20, 52 more genes
nsv5673945	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr8: 133,141,509-134,296,554 , GRCh38.p12 chr8: 132,129,262-133,284,311	DNAAF11, SLA, 15 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	DNAAF11, 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	DNAAF11, 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	DNAAF11, 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	DNAAF11, 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	DNAAF11, 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	DNAAF11, 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	DNAAF11, LOC105375890, 2105 more genes
nsv3923310	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098	DNAAF11, LOC112268023, 2105 more genes
nsv3914307	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,605-146,280,167 , GRCh38 chr8: 241,605-145,054,781 , NCBI36 chr8: 181,605-146,250,971	DNAAF11, LOC107986897, 2104 more genes
nsv3919282	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824	DNAAF11, MIR4662B, 2104 more genes
nsv3919200	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639	DNAAF11, LOC112268023, 2103 more genes
nsv3906425	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 12,490,999-146,295,771 , GRCh38.p12 chr8: 12,633,490-145,070,385	DNAAF11, LOC112268016, 1819 more genes
nsv3915762	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 21,193,313-146,266,575 , GRCh38 chr8: 21,291,522-145,070,385 , GRCh37 chr8: 21,149,033-146,295,771	DNAAF11, LOC105375693, 1718 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 62

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Number of Variants: 20

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