auts2[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
nsv6313578	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 69,145,364-70,023,881 , GRCh38.p12 chr7: 69,680,378-70,558,895	AUTS2
nsv3921333	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 68,768,173-69,374,770 , GRCh38 chr7: 69,665,251-70,271,848 , GRCh37 chr7: 69,130,237-69,736,834	AUTS2
nsv3876238	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 69,899,499-70,435,751 , GRCh37.p13 chr7: 69,364,485-69,900,737	AUTS2
nsv3897425	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 69,325,515-69,644,230 , GRCh38.p12 chr7: 69,860,529-70,179,244	AUTS2
nsv3893146	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 69,617,684-69,932,353 , GRCh38.p12 chr7: 70,152,698-70,467,367	AUTS2
nsv3920457	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 70,206,515-70,493,590 , NCBI36 chr7: 69,309,437-69,596,512 , GRCh37 chr7: 69,671,501-69,958,576	AUTS2
nsv4457328	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 69,220,855-69,449,057 , GRCh38.p12 chr7: 69,755,869-69,984,071	AUTS2
nsv3911233	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 68,931,633-69,141,367 , GRCh37 chr7: 69,293,697-69,503,431 , GRCh38 chr7: 69,828,711-70,038,445	AUTS2
nsv4455452	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 69,274,353-69,464,494 , GRCh38.p12 chr7: 69,809,367-69,999,508	AUTS2
nsv3917821	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 68,968,673-69,158,502 , GRCh38 chr7: 69,865,751-70,055,580 , GRCh37 chr7: 69,330,737-69,520,566	AUTS2
nsv3892777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 69,248,785-69,438,070 , GRCh38.p12 chr7: 69,783,799-69,973,084	AUTS2
nsv3923929	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 69,765,424-69,912,439 , NCBI36 chr7: 69,403,360-69,550,375 , GRCh38 chr7: 70,300,438-70,447,453	AUTS2
nsv3904433	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 69,892,610-70,037,666 , GRCh38.p12 chr7: 70,427,624-70,572,680	AUTS2
nsv6313645	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 69,527,664-69,647,986 , GRCh38.p12 chr7: 70,062,678-70,183,000	AUTS2
nsv4675686	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 69,489,582-69,603,832 , GRCh38.p12 chr7: 70,024,596-70,138,846	AUTS2
nsv4675797	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 69,532,233-69,644,230 , GRCh38.p12 chr7: 70,067,247-70,179,244	AUTS2
nsv3907953	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 69,867,672-69,957,025 , GRCh38.p12 chr7: 70,402,686-70,492,039	AUTS2
nsv3890475	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 69,307,298-69,395,898 , GRCh38.p12 chr7: 69,842,312-69,930,912	AUTS2
nsv3892401	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 69,063,905-69,105,486 , GRCh38.p12 chr7: 69,598,919-69,640,500	AUTS2
nsv3921485	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 68,935,186-68,968,732 , GRCh38 chr7: 69,832,264-69,865,810 , GRCh37 chr7: 69,297,250-69,330,796	AUTS2

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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 117

Page of 6

Number of Variants: 20

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Supplemental Content

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