drc7[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
nsv3894127	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 57,723,179-57,729,431 , GRCh38.p12 chr16: 57,689,267-57,695,519	DRC7, ADGRG3
nsv3890883	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 57,723,197-57,729,431 , GRCh38.p12 chr16: 57,689,285-57,695,519	DRC7, ADGRG3
nsv3891925	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 57,722,866-57,727,719 , GRCh38.p12 chr16: 57,688,954-57,693,807	DRC7, ADGRG3
nsv3890217	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 57,722,866-57,727,463 , GRCh38.p12 chr16: 57,688,954-57,693,551	DRC7, ADGRG3
nsv3893688	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 57,723,179-57,727,463 , GRCh38.p12 chr16: 57,689,267-57,693,551	DRC7, ADGRG3
nsv3916542	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 55,457,477-63,841,622 , NCBI36 chr16: 54,048,890-62,433,027 , GRCh37 chr16: 55,491,389-63,875,526	DRC7, CES1, 139 more genes
nsv3908644	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 56,950,941-60,203,590 , GRCh38.p12 chr16: 56,917,029-60,169,686	DRC7, ADGRG1, 75 more genes
nsv7095031	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 56,226,148-58,768,132 , GRCh38.p12 chr16: 56,192,236-58,734,228	DRC7, MT1B, 92 more genes
nsv7094589	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 57,016,057-58,768,132 , GRCh38.p12 chr16: 56,982,145-58,734,228	DRC7, SLC38A7, 58 more genes
nsv3906108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224	DRC7, CKLF, 1882 more genes
nsv3904593	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973	DRC7, LOC100128079, 1879 more genes
nsv3901410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287	DRC7, LINC02175, 1877 more genes
nsv3909417	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867	DRC7, PRSS53, 1868 more genes
nsv3892266	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654	DRC7, FTLP14, 1868 more genes
nsv3921269	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345	DRC7, LOC105371237, 985 more genes
nsv6314755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654	DRC7, ATMIN, 826 more genes
nsv3915506	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 51,490,596-88,682,563 , GRCh38 chr16: 52,899,183-90,088,654 , GRCh37 chr16: 52,933,095-90,155,062	DRC7, CFAP69P1, 716 more genes
nsv3891306	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 57,051,473-89,797,669 , GRCh38.p12 chr16: 57,017,561-89,731,261	DRC7, LOC107984894, 613 more genes
nsv3895555	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 34,197,492-64,509,054 , GRCh38.p12 chr16: 34,963,121-64,475,151	DRC7, RSPRY1, 362 more genes
nsv3918521	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 48,276,933-66,993,116 , GRCh37 chr16: 49,719,432-68,435,615 , GRCh38 chr16: 49,685,521-68,401,712	DRC7, CYLD-AS2, 342 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 43

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Number of Variants: 20

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Supplemental Content

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