dbVar for Gene (Select 105370169) - 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
nsv5935280	copy number variation	1	nstd209	human		GRCh38 chr13: 39,071,008-39,097,672 , GRCh37.p13 chr13: 39,645,145-39,671,809	LOC105370169
nsv5865564	copy number variation	1	nstd209	human		GRCh38 chr13: 39,070,770-39,096,794 , GRCh37.p13 chr13: 39,644,907-39,670,931	LOC105370169
nsv5564510	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053	RN7SL272P, DIAPH3, 1333 more genes
nsv4729423	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 39,531,602-40,152,084 , GRCh38.p12 chr13: 38,957,465-39,577,947	LOC105370169, PROSER1, 8 more genes
nsv4365837	copy number variation	1	nstd173	human		GRCh37 chr13: 39,535,359-39,741,853 , GRCh38.p12 chr13: 38,961,222-39,167,716	NXT1P1, NHLRC3, 3 more genes
nsv3924676	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862	GRTP1, FABP5P1, 1334 more genes
nsv3924246	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 29,785,946-38,739,818 , GRCh37 chr13: 30,887,946-39,841,818 , GRCh38 chr13: 30,313,809-39,267,681	LINC01048, N4BP2L2-IT2, 117 more genes
nsv3923911	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 38,438,363-68,537,920 , GRCh38 chr13: 37,864,226-67,963,788 , NCBI36 chr13: 37,336,363-67,435,921	MLNR, SIAH3, 422 more genes
nsv3923636	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 37,986,314-50,897,351 , GRCh37 chr13: 39,088,314-51,999,350 , GRCh38 chr13: 38,514,177-51,425,214	TUSC8, SNORA31B, 251 more genes
nsv3922463	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 18,418,322-114,088,205 , GRCh37 chr13: 19,520,322-115,070,103 , GRCh38 chr13: 18,946,182-114,304,628	TULP3P1, LOC105370349, 1311 more genes
nsv3921404	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 31,592,297-49,065,340 , GRCh38 chr13: 31,018,160-48,491,204 , NCBI36 chr13: 30,490,297-47,963,341	MIR8079, ZDHHC4P1, 280 more genes
nsv3921223	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 19,671,934-114,340,331 , NCBI36 chr13: 19,144,074-114,123,908 , GRCh37 chr13: 20,246,074-115,085,141	TRIM60P13, LINC00351, 1289 more genes
nsv3920749	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 20,407,270-115,064,089 , GRCh38 chr13: 19,833,130-114,298,614 , NCBI36 chr13: 19,305,270-114,082,191	DIAPH3-AS2, LOC105370216, 1281 more genes
nsv3920039	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr13: 31,937,609-91,227,546 , NCBI36 chr13: 30,835,609-90,025,547 , GRCh38 chr13: 31,363,472-90,575,292	PSMD10P3, CPB2, 714 more genes
nsv3919574	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,850,545-114,327,173 , GRCh37 chr13: 19,296,527-115,085,141 , NCBI36 chr13: 18,194,527-114,110,750	RNU6-77P, LINC00457, 1317 more genes
nsv3919427	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 31,025,745-64,942,500 , GRCh37 chr13: 32,127,745-66,044,499 , GRCh38 chr13: 31,553,608-65,470,367	PCDH8, TRIM13, 469 more genes
nsv3917322	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr13: 19,309,535-114,110,750 , GRCh37 chr13: 20,411,535-115,085,141 , GRCh38 chr13: 19,837,395-114,327,173	RNY1P7, LINC01039, 1283 more genes
nsv3917270	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 33,105,623-87,409,299 , NCBI36 chr13: 32,003,623-86,207,300 , GRCh38 chr13: 32,531,486-86,757,044	LINC00366, PPIAP26, 663 more genes
nsv3916629	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,139,188-115,085,141 , NCBI36 chr13: 18,037,188-114,110,750 , GRCh38 chr13: 18,565,048-114,327,173	TM9SF2, LOC107984564, 1330 more genes
nsv3916116	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 19,305,270-114,110,683 , GRCh38 chr13: 19,833,130-114,327,106 , GRCh37 chr13: 20,407,270-115,085,141	LOC105370263, RPS7P10, 1283 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

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Study Type

Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 113

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Number of Variants: 20

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