nsun7[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
nsv3876868	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 40,670,323-40,779,968 , GRCh38.p12 chr4: 40,668,306-40,777,951	NSUN7
nsv3883869	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 40,686,808-40,788,567 , GRCh38.p12 chr4: 40,684,791-40,786,550	NSUN7, ARL4AP2
nsv3872997	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 40,686,808-40,788,093 , GRCh38.p12 chr4: 40,684,791-40,786,076	NSUN7, ARL4AP2
nsv3912786	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 40,371,405-40,488,883 , GRCh37.p13 chr4: 40,676,648-40,794,126 , GRCh38.p12 chr4: 40,674,631-40,792,109	NSUN7, ARL4AP2
nsv7137048	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 40,337,485-41,941,400 , GRCh38.p12 chr4: 40,335,468-41,939,383	NSUN7, RNU6-1195P, 23 more genes
nsv3873978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724	NSUN7, LOC100422029, 2358 more genes
nsv3876533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611	NSUN7, LOC100420289, 2347 more genes
nsv3884499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286	NSUN7, MTND4LP29, 2341 more genes
nsv3880085	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318	NSUN7, LOC112268460, 2345 more genes
nsv3883791	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495	NSUN7, LOC105377343, 2341 more genes
nsv3872797	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-66,440,622 , GRCh38.p12 chr4: 68,453-65,574,904	NSUN7, GNPDA2, 813 more genes
nsv7148157	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396	NSUN7, OR7E84P, 764 more genes
nsv4684161	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-49,620,898 , GRCh38.p12 chr4: 49,556-49,618,881	NSUN7, TLR10, 669 more genes
nsv7148161	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194	NSUN7, SLIRPP2, 659 more genes
nsv3876307	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,440-49,064,044 , GRCh38.p12 chr4: 12,440-49,062,027	NSUN7, ADGRA3, 659 more genes
nsv6634358	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344	NSUN7, LINC02475, 658 more genes
nsv3875629	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344	NSUN7, LOC105374433, 658 more genes
nsv3880889	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 1,356,924-49,659,859 , GRCh38.p12 chr4: 1,363,136-49,657,842	NSUN7, LOC107986262, 619 more genes
nsv3916848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 36,424-47,493,612 , GRCh38 chr4: 36,424-47,491,595 , NCBI36 chr4: 26,424-47,188,369	NSUN7, MIR943, 634 more genes
nsv6315440	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 114,784-47,569,569 , GRCh38.p12 chr4: 114,902-47,567,552	NSUN7, FAM86KP, 631 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 26

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Number of Variants: 20

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Supplemental Content

Find related data

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