SAMN00001259 AND estd199 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
esv2667872	copy number variation	147	estd199	human	GRCh37 chr1: 225,133,630-225,248,654 , GRCh38.p12 chr1: 224,945,928-225,060,952	DNAH14
esv2665996	copy number variation	112	estd199	human	GRCh37 chr4: 34,779,980-34,829,038 , GRCh38.p12 chr4: 34,778,358-34,827,416 , GRCh38.p12 chr4\|NW_003315915.1: 270,687-319,745	LOC105378262
esv2666739	copy number variation	325	estd199	human	GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547	CR1
esv2668226	copy number variation	311	estd199	human	GRCh37 chr3: 129,763,245-129,799,692 , GRCh38.p12 chr3: 130,044,402-130,080,849	ALG1L2
esv2673583	copy number variation	519	estd199	human	GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395	SIRPB1
esv2676662	copy number variation	263	estd199	human	GRCh37 chr19: 41,360,712-41,392,496 , GRCh38.p12 chr19: 40,854,807-40,886,591	CYP2A7
esv2660568	copy number variation	4	estd199	human	GRCh37 chr19: 40,367,092-40,399,033 , GRCh38.p12 chr19\|NW_009646206.1: 136,328-157,795 , GRCh38.p12 chr19: 39,876,452-39,897,919	FCGBP
esv2669475	copy number variation	624	estd199	human	GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086	RNVU1-19
esv2667383	copy number variation	138	estd199	human	GRCh37 chr2: 98,139,645-98,158,592 , GRCh38.p12 chr2: 97,523,182-97,542,129	ANKRD36B
esv2663133	copy number variation	46	estd199	human	GRCh37 chr6: 32,629,745-32,648,392 , GRCh38.p12 chr6: 32,661,968-32,680,615	HLA-DQB1
esv2674647	copy number variation	204	estd199	human	GRCh37 chr8: 56,377,729-56,393,641 , GRCh38.p12 chr8: 55,465,169-55,481,081	XKR4
esv2663811	copy number variation	483	estd199	human	GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
esv2656701	copy number variation	437	estd199	human	GRCh37 chr16: 78,371,638-78,384,898 , GRCh38.p12 chr16: 78,337,741-78,351,001	WWOX
esv2664803	copy number variation	436	estd199	human	GRCh37 chr15: 76,884,596-76,896,938 , GRCh38.p12 chr15: 76,592,255-76,604,597	SCAPER
esv2678677	copy number variation	179	estd199	human	GRCh37 chr15: 76,884,295-76,895,742 , GRCh38.p12 chr15: 76,591,954-76,603,401	SCAPER
esv2668861	copy number variation	64	estd199	human	GRCh37 chr9: 6,700,452-6,710,572 , GRCh38.p12 chr9: 6,700,452-6,710,572	LINC02851
esv2673551	copy number variation	872	estd199	human	GRCh37 chr3: 192,875,329-192,885,405 , GRCh38.p12 chr3: 193,157,540-193,167,616	VEZF1P1
esv2677090	copy number variation	28	estd199	human	GRCh37 chr9: 6,701,595-6,711,642 , GRCh38.p12 chr9: 6,701,595-6,711,642	LINC02851
esv2675979	copy number variation	520	estd199	human	GRCh37 chr6: 53,924,803-53,934,828 , GRCh38.p12 chr6: 54,060,005-54,070,030	MLIP
esv2657260	copy number variation	826	estd199	human	GRCh37 chr2: 87,730,745-87,740,792 , GRCh38.p12 chr2: 87,431,226-87,441,083	LINC01943

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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 840

Page of 42

Number of Variants: 20

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Supplemental Content

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