moon - 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
nsv5059992	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,244,921-117,252,122 , GRCh38 chr7: 117,604,867-117,612,068	CFTR
nsv997145	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 44,732,421-44,971,857 , GRCh38.p12 chrX: 44,873,175-45,112,612	KDM6A
nsv997170	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 135,067,583-135,129,428 , GRCh38.p12 chrX: 135,985,424-136,047,269	SLC9A6
nsv997177	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 119,658,444-119,709,684 , GRCh38.p12 chrX: 120,524,589-120,575,829	CUL4B
nsv997180	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 118,967,989-118,986,991 , GRCh38.p12 chrX: 119,834,026-119,853,028	UPF3B
esv1995006	copy number variation	1	estd194	human		NCBI36 chr1: 2,577,543-2,599,245 , GRCh37.p13 chr1: 2,587,683-2,609,385 , GRCh38.p12 chr1: 2,656,244-2,677,946 , GRCh38.p12 chr1\|NT_187515.1: 219,010-238,521	TTC34
esv2244500	copy number variation	1	estd194	human		NCBI36 chr3: 181,869,489-181,889,386 , GRCh37.p13 chr3: 180,386,795-180,406,692 , GRCh38.p12 chr3: 180,669,007-180,688,904	CCDC39
esv2322180	copy number variation	1	estd194	human		NCBI36 chr6: 28,872,654-28,888,557 , GRCh37.p13 chr6\|NT_167247.1: 68,076-83,979 , GRCh37.p13 chr6\|NT_167244.1: 68,076-83,979 , GRCh37.p13 chr6: 28,764,675-28,780,578 , GRCh37.p13 chr6\|NT_167245.1: 68,072-83,988 , GRCh37.p13 chr6\|NT_167248.1: 68,076-83,979 , GRCh38.p12 chr6\|NT_167247.2: 62,491-78,394 , GRCh38.p12 chr6\|NT_167245.2: 62,487-78,403 , GRCh38.p12 chr6\|NT_167244.2: 62,477-78,380 , GRCh38.p12 chr6: 28,796,898-28,812,801 , GRCh38.p12 chr6\|NT_167246.2: 62,467-78,368	TRF-GAA3-1
esv2295153	copy number variation	1	estd194	human		NCBI36 chrX: 55,189,366-55,204,332 , GRCh37.p13 chrX: 55,172,641-55,187,607 , GRCh38.p12 chrX: 55,146,208-55,161,174	VCF2
esv2076042	copy number variation	1	estd194	human		NCBI36 chr16: 76,928,949-76,942,596 , GRCh37.p13 chr16: 78,371,448-78,385,095 , GRCh38.p12 chr16: 78,337,551-78,351,198	WWOX
esv2263886	copy number variation	1	estd194	human		NCBI36 chrX: 55,189,274-55,202,368 , GRCh37.p13 chrX: 55,172,549-55,185,643 , GRCh38.p12 chrX: 55,146,116-55,159,210	VCF2
esv2409223	copy number variation	1	estd194	human		NCBI36 chrX: 55,189,322-55,202,391 , GRCh37.p13 chrX: 55,172,597-55,185,666 , GRCh38.p12 chrX: 55,146,164-55,159,233	VCF2
esv2349622	copy number variation	1	estd194	human		NCBI36 chr4: 33,851,281-33,863,497 , GRCh37.p13 chr4: 34,174,886-34,187,102 , GRCh38.p12 chr4: 34,173,264-34,185,480	LINC02484
esv2232855	copy number variation	1	estd194	human		NCBI36 chr7: 10,523,105-10,534,413 , GRCh37.p13 chr7: 10,556,580-10,567,888 , GRCh38.p12 chr7: 10,516,953-10,528,261	MGC4859
esv2314060	copy number variation	1	estd194	human		NCBI36 chr7: 48,362,088-48,372,605 , GRCh37.p13 chr7: 48,391,542-48,402,059 , GRCh38.p12 chr7: 48,351,945-48,362,462	ABCA13
esv2415465	copy number variation	1	estd194	human		NCBI36 chr3: 194,357,858-194,368,292 , GRCh37.p13 chr3: 192,875,164-192,885,598 , GRCh38.p12 chr3: 193,157,375-193,167,809	VEZF1P1
esv2159853	copy number variation	1	estd194	human		NCBI36 chr8: 63,377,769-63,387,944 , GRCh37.p13 chr8: 63,215,215-63,225,390 , GRCh38.p12 chr8: 62,302,656-62,312,831	NKAIN3
esv2388810	copy number variation	1	estd194	human		NCBI36 chr20: 15,258,762-15,268,773 , GRCh37.p13 chr20: 15,310,762-15,320,773 , GRCh38.p12 chr20: 15,330,116-15,340,127	MACROD2
esv2161601	copy number variation	1	estd194	human		NCBI36 chr6: 136,642,626-136,652,627 , GRCh37.p13 chr6: 136,600,933-136,610,934 , GRCh38.p12 chr6: 136,279,795-136,289,796	BCLAF1
esv2298302	copy number variation	1	estd194	human		NCBI36 chr6: 72,920,417-72,930,379 , GRCh37.p13 chr6: 72,863,696-72,873,658 , GRCh38.p12 chr6: 72,153,993-72,163,955	RIMS1

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Result Filters

Object Type

Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 504922

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Number of Variants: 20

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