nsg2[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
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	NSG2, MEGF10, 2080 more genes
nsv3914710	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 172,961,091-175,054,665 , GRCh37 chr5: 172,388,094-174,481,668 , NCBI36 chr5: 172,320,700-174,414,274	NSG2, NKX2-5, 40 more genes
nsv3919616	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 172,203,801-173,769,972 , GRCh38 chr5: 172,776,798-174,342,969 , NCBI36 chr5: 172,136,407-173,702,578	NSG2, LINC02995, 33 more genes
nsv3917911	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 173,309,382-174,260,004 , GRCh37 chr5: 173,376,776-174,327,398 , GRCh38 chr5: 173,949,773-174,900,395	NSG2, HIGD1AP3, 13 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	NSG2, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	NSG2, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	NSG2, SPEF2, 2490 more genes
nsv3874238	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337	NSG2, PJA2, 1228 more genes
nsv6315448	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788	NSG2, GRM6, 554 more genes
nsv3921182	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 149,094,155-180,699,152 , GRCh38 chr5: 149,714,592-181,272,151 , NCBI36 chr5: 149,074,348-180,631,758	NSG2, RN7SKP148, 553 more genes
nsv3885523	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 155,344,802-180,693,344 , GRCh38.p12 chr5: 155,917,792-181,266,343	NSG2, WWC1, 446 more genes
nsv3924400	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 156,185,101-180,629,412 , GRCh37 chr5: 156,252,523-180,696,806 , GRCh38 chr5: 156,825,512-181,269,805	NSG2, CEP192P1, 443 more genes
nsv3921186	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 164,386,701-181,269,805 , GRCh37 chr5: 163,813,707-180,696,806 , NCBI36 chr5: 163,746,285-180,629,412	NSG2, TENM2, 347 more genes
nsv3920339	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 164,323,950-180,629,412 , GRCh37.p13 chr5: 164,391,372-180,696,806 , GRCh38.p12 chr5: 164,964,366-181,269,805	NSG2, MIR1229, 343 more genes
nsv3918887	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 168,761,759-180,712,302 , NCBI36 chr5: 168,694,337-180,644,908 , GRCh38 chr5: 169,334,755-181,285,301	NSG2, RPS8P7, 311 more genes
nsv6634369	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788	NSG2, GFPT2, 287 more genes
nsv4768375	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 170,805,664-180,719,789 , GRCh38.p12 chr5: 171,378,660-181,292,788	NSG2, LINC01863, 279 more genes
nsv3874802	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 172,031,248-180,719,789 , GRCh38.p12 chr5: 172,604,245-181,292,788	NSG2, LINC01863, 257 more genes
nsv3924705	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 173,237,772-176,614,618 , GRCh37 chr5: 172,664,775-176,041,619 , NCBI36 chr5: 172,597,381-175,974,225	NSG2, RNF44, 62 more genes
nsv3884275	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 94,844,077-178,830,410 , GRCh38.p12 chr5: 95,508,373-179,403,409	NSG2, LOC107986368, 1258 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 22

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Number of Variants: 20

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