csgalnact2[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
nsv3898267	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 43,439,353-43,680,587 , GRCh38.p12 chr10: 42,943,905-43,185,139	CSGALNACT2, MIR5100, 2 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	CSGALNACT2, RNU7-12P, 1876 more genes
nsv3906389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996	CSGALNACT2, LOC100419870, 2105 more genes
nsv3891157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558	CSGALNACT2, AGAP14P, 2097 more genes
nsv3902271	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639	CSGALNACT2, ANXA11, 2085 more genes
nsv3891958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414	CSGALNACT2, TUBB8, 2085 more genes
nsv7137211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639	CSGALNACT2, EXOC6, 1906 more genes
nsv3904390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 100,026-50,961,640 , GRCh38.p12 chr10: 54,086-49,753,594	CSGALNACT2, LINC00700, 806 more genes
nsv3917047	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 42,500,760-75,145,672 , GRCh37 chr10: 43,180,754-75,475,666 , GRCh38 chr10: 42,685,306-73,715,908	CSGALNACT2, SLC9A3P3, 476 more genes
nsv3921181	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 41,927,641-68,830,439 , GRCh38 chr10: 42,112,187-67,400,675 , GRCh37 chr10: 42,607,635-69,160,433	CSGALNACT2, AGAP6, 338 more genes
nsv3919301	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 43,277,502-55,351,191 , GRCh37.p13 chr10: 43,957,496-55,681,185 , GRCh38.p12 chr10: 38,980,309-49,959,916	CSGALNACT2, FAM245B, 196 more genes
nsv3916253	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 42,884,294-52,265,317 , NCBI36 chr10: 42,699,748-53,695,083 , GRCh37 chr10: 43,379,742-54,025,077	CSGALNACT2, PTPN20CP, 198 more genes
nsv3918611	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 42,395,201-50,877,059 , NCBI36 chr10: 42,210,655-52,306,825 , GRCh37 chr10: 42,890,649-52,636,819	CSGALNACT2, LOC105378289, 211 more genes
nsv3972353	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 37,149,872-46,169,876 , GRCh38.p12 chr10: 36,860,944-45,674,428	CSGALNACT2, ALOX5, 132 more genes
nsv3923539	inversion	1	nstd102	human	Likely pathogenic	GRCh38.p12 chr10: 43,115,743-59,903,521 , GRCh37 chr10: 43,611,191-61,663,279	CSGALNACT2, ALOX5, 248 more genes
nsv3920598	copy number variation	1	nstd102	human	Benign	NCBI36 chr10: 4,636,926-47,125,152 , GRCh38 chr10: 4,604,734-48,074,662 , GRCh37 chr10: 4,646,926-47,531,169	CSGALNACT2, LOC100420467, 709 more genes
nsv3907664	copy number variation	1	nstd102	human	drug response	GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422	CSGALNACT2, SHOC2, 1487 more genes
nsv3917122	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr10: 42,942,157-43,188,362 , GRCh38 chr10: 43,126,703-43,372,908 , GRCh37 chr10: 43,622,151-43,868,356	CSGALNACT2, LOC107984225, 7 more genes
nsv6290893	copy number variation	1	nstd102	human	not provided	GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579	CSGALNACT2, C1QL3, 774 more genes
nsv3893701	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 42,706,947-44,489,498 , GRCh38.p12 chr10: 42,211,499-43,994,050	CSGALNACT2, LOC107984165, 57 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 21

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Number of Variants: 20

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