afdn[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
nsv3905011	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 168,225,290-168,265,762 , GRCh38.p12 chr6: 167,824,610-167,865,082	AFDN, AFDN-DT
nsv3911475	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 152,793,402-170,610,394 , GRCh37 chr6: 153,114,537-170,919,482 , NCBI36 chr6: 153,156,230-170,761,407	AFDN, SNORA116, 275 more genes
nsv3913213	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 154,118,058-170,602,152 , NCBI36 chr6: 154,480,885-170,753,165 , GRCh37 chr6: 154,439,193-170,911,240	AFDN, LDHAL6FP, 258 more genes
nsv3921695	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 154,539,655-170,714,507 , NCBI36 chr6: 154,902,481-170,865,520 , GRCh37 chr6: 154,860,789-171,023,595	AFDN, LOC105378128, 255 more genes
nsv6315428	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 159,121,459-170,919,482 , GRCh38.p12 chr6: 158,700,427-170,610,394	AFDN, TBP, 200 more genes
nsv3921491	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 159,795,661-170,763,014 , GRCh38 chr6: 159,454,639-170,612,001 , GRCh37 chr6: 159,875,671-170,921,089	AFDN, LOC102724357, 183 more genes
nsv1397956	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 159,830,469-170,673,013 , GRCh37.p13 chr6: 159,910,479-170,831,088 , GRCh38.p12 chr6: 159,489,447-170,522,000	AFDN, LOC107986675, 179 more genes
nsv3918679	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 160,336,422-171,023,595 , NCBI36 chr6: 160,256,412-170,865,520 , GRCh38 chr6: 159,915,390-170,714,507	AFDN, FAM120B, 172 more genes
nsv3923088	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 160,246,945-170,921,089 , NCBI36 chr6: 160,166,935-170,763,014 , GRCh38 chr6: 159,825,913-170,612,001	AFDN, DKFZp451B082, 169 more genes
nsv3917206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 160,780,718-170,917,906 , NCBI36 chr6: 160,700,708-170,759,831 , GRCh38 chr6: 160,359,686-170,608,818	AFDN, LINC02544, 161 more genes
nsv3912310	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 160,825,832-170,763,024 , GRCh38 chr6: 160,484,810-170,612,011 , GRCh37 chr6: 160,905,842-170,921,099	AFDN, LOC102724152, 160 more genes
nsv1398077	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 160,991,083-170,899,992 , GRCh37.p13 chr6: 161,071,093-171,055,067 , GRCh38.p12 chr6: 160,650,061-170,745,979	AFDN, LOC107986549, 163 more genes
nsv6313560	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 161,047,873-170,919,482 , GRCh38.p12 chr6: 160,626,841-170,610,394	AFDN, LOC105378142, 159 more genes
nsv3917590	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 161,240,920-170,761,407 , GRCh37 chr6: 161,320,930-170,919,482 , GRCh38 chr6: 160,899,898-170,610,394	AFDN, LOC105378143, 155 more genes
nsv7148156	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 161,349,282-170,584,790 , GRCh37.p13 chr6: 161,770,314-170,893,878	AFDN, LOC105378126, 149 more genes
nsv3895890	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 162,381,975-170,919,482 , GRCh38.p12 chr6: 161,960,943-170,610,394	AFDN, LOC105378118, 148 more genes
nsv4675923	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 162,452,035-170,919,482 , GRCh38.p12 chr6: 162,031,003-170,610,394	AFDN, TRE-TTC15-1, 148 more genes
nsv3917830	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 162,463,878-170,917,906 , NCBI36 chr6: 162,383,868-170,759,831 , GRCh38 chr6: 162,042,846-170,608,818	AFDN, LOC285804, 148 more genes
nsv4675281	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 162,661,108-170,919,482 , GRCh38.p12 chr6: 162,240,076-170,610,394	AFDN, LOC105378127, 148 more genes
nsv1398287	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 162,784,565-170,899,992 , GRCh37.p13 chr6: 162,864,575-171,055,067 , GRCh38.p12 chr6: 162,443,543-170,745,979	AFDN, LINC02544, 150 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 80

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Number of Variants: 20

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