ccser2[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
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	CCSER2, RNU7-12P, 1876 more genes
nsv3920295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422	CCSER2, EIF2S2P3, 895 more genes
nsv6637542	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 82,595,472-93,542,416 , GRCh38.p12 chr10: 80,835,716-91,782,659	CCSER2, IFIT6P, 166 more genes
nsv3891568	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 83,379,241-93,219,169 , GRCh38.p12 chr10: 81,619,485-91,459,412	CCSER2, NAPGP1, 157 more genes
nsv6634458	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 83,533,660-91,913,077 , GRCh38.p12 chr10: 81,773,904-90,153,320	CCSER2, IFIT5, 140 more genes
nsv4729484	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 81,457,752-89,253,430 , GRCh38.p12 chr10: 79,697,996-87,493,673	CCSER2, DPY19L2P5, 115 more genes
nsv3923084	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,149,191-89,108,131 , GRCh38 chr10: 79,719,429-87,358,394 , GRCh37 chr10: 81,479,185-89,118,151	CCSER2, LINC02650, 110 more genes
nsv3910996	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,541,288-89,108,131 , GRCh38 chr10: 79,802,022-87,358,394 , GRCh37 chr10: 81,561,459-89,118,151	CCSER2, HMGN2P8, 110 more genes
nsv3910032	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 81,449,116-88,983,530 , NCBI36 chr10: 81,119,122-88,973,510 , GRCh38 chr10: 79,689,360-87,223,773	CCSER2, LINC02655, 109 more genes
nsv4729317	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 81,617,260-89,146,780 , GRCh38.p12 chr10: 79,857,504-87,387,023	CCSER2, LOC105378390, 109 more genes
nsv4728260	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 81,585,301-89,101,700 , GRCh38.p12 chr10: 79,825,545-87,341,943	CCSER2, C1DP3, 109 more genes
nsv3910650	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,648,252-89,108,131 , GRCh38 chr10: 79,898,516-87,358,394 , GRCh37 chr10: 81,658,272-89,118,151	CCSER2, ZNRF2P3, 103 more genes
nsv3891947	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 81,617,260-88,980,961 , GRCh38.p12 chr10: 79,857,504-87,221,204	CCSER2, RNU1-65P, 104 more genes
nsv3897099	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 81,597,767-88,951,347 , GRCh38.p12 chr10: 79,838,011-87,191,590	CCSER2, NRG3, 104 more genes
nsv6315478	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 81,630,468-88,980,961 , GRCh38.p12 chr10: 79,870,712-87,221,204	CCSER2, RNU1-19P, 102 more genes
nsv3911129	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 81,640,994-88,940,429 , GRCh38 chr10: 79,881,238-87,180,672 , NCBI36 chr10: 81,630,974-88,930,409	CCSER2, LOC100130698, 99 more genes
nsv3922892	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 79,802,022-87,068,261 , GRCh37 chr10: 81,561,459-88,828,018 , NCBI36 chr10: 81,263,385-88,817,998	CCSER2, LINC02655, 103 more genes
nsv3922465	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 81,658,272-88,869,584 , GRCh38 chr10: 79,898,516-87,109,827 , NCBI36 chr10: 81,648,252-88,859,564	CCSER2, FARSBP1, 97 more genes
nsv3918925	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,631,898-88,817,998 , GRCh38 chr10: 79,882,162-87,068,261 , GRCh37 chr10: 81,641,918-88,828,018	CCSER2, LOC105378387, 97 more genes
nsv3891414	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 82,013,260-89,166,455 , GRCh38.p12 chr10: 80,253,504-87,406,698	CCSER2, LOC105378392, 90 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 46

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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