SAMN00007734 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
esv2669002	copy number variation	1	estd199	human	GRCh37 chrX: 32,721,084-32,810,360 , GRCh38.p12 chrX: 32,702,967-32,792,243	DMD
esv2676879	copy number variation	198	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
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
esv2663673	copy number variation	27	estd199	human	GRCh37 chr13: 57,865,913-57,892,004 , GRCh38.p12 chr13: 57,291,779-57,317,870	SLC25A5P4
esv2661219	copy number variation	458	estd199	human	GRCh37 chr8: 48,180,445-48,214,692 , GRCh38.p12 chr8: 47,276,396-47,302,103	SPIDR
esv2661915	copy number variation	81	estd199	human	GRCh37 chr6: 77,437,226-77,458,987 , GRCh38.p12 chr6: 76,727,509-76,749,270	LOC105377861
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
esv2664400	copy number variation	3	estd199	human	GRCh37 chr1: 246,368,884-246,388,773 , GRCh38.p12 chr1: 246,205,582-246,225,471	SMYD3
esv2662007	copy number variation	32	estd199	human	GRCh37 chr10: 122,769,701-122,787,511 , GRCh38.p12 chr10: 121,010,188-121,027,998	LOC105378521
esv2661457	copy number variation	8	estd199	human	GRCh37 chr7: 102,351,566-102,367,905 , GRCh38.p12 chr7: 102,711,119-102,727,458	RASA4DP
esv2663679	copy number variation	1	estd199	human	GRCh37 chr22: 31,895,423-31,911,076 , GRCh38.p12 chr22: 31,499,437-31,515,090	SFI1
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
esv2670596	copy number variation	22	estd199	human	GRCh37 chr4: 151,874,295-151,885,892 , GRCh38.p12 chr4: 150,953,143-150,964,740	LRBA
esv2666384	copy number variation	1	estd199	human	GRCh37 chr8: 114,141,314-114,151,600 , GRCh38.p12 chr8: 113,129,085-113,139,371	CSMD3
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
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
esv2662223	copy number variation	5	estd199	human	GRCh37 chr4: 187,880,502-187,889,752 , GRCh38.p12 chr4: 186,959,348-186,968,598	LOC102723906
esv2667386	copy number variation	15	estd199	human	GRCh37 chr19: 56,713,363-56,722,147 , GRCh38.p12 chr19: 56,201,994-56,210,778	ZSCAN5C

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 1582

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Number of Variants: 20

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