178826 AND nstd173 - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv4385648	copy number variation	43	nstd173	human	GRCh37 chr20: 1,560,774-1,593,836 , GRCh38.p12 chr20: 1,580,128-1,613,190	SIRPB1
nsv4384133	copy number variation	106	nstd173	human	GRCh37 chr1: 169,216,044-169,241,765 , GRCh38.p12 chr1: 169,246,806-169,272,527	NME7
nsv4365093	copy number variation	508	nstd173	human	GRCh37 chr13: 57,758,269-57,778,379 , GRCh38.p12 chr13: 57,184,135-57,204,245	MTCO2P3
nsv4372929	copy number variation	6	nstd173	human	GRCh37 chr6: 294,911-380,993 , GRCh38.p12 chr6: 294,911-380,993	DUSP22
nsv4369227	copy number variation	203	nstd173	human	GRCh37 chr1: 72,771,366-72,811,904 , GRCh38.p12 chr1: 72,305,683-72,346,221 , GRCh38.p12 chr1\|NW_018654707.1: 17,950-67,446	LOC105378797
nsv4380338	copy number variation	10	nstd173	human	GRCh37 chr7: 146,216,848-146,254,889 , GRCh38.p12 chr7: 146,519,756-146,557,797	CNTNAP2
nsv4369305	copy number variation	11	nstd173	human	GRCh37 chr11: 18,941,197-18,971,379 , GRCh38.p12 chr11: 18,919,650-18,949,832	MRGPRX1
nsv4376456	copy number variation	1782	nstd173	human	GRCh37 chr8: 39,246,772-39,386,964 , GRCh38.p12 chr8: 39,389,253-39,529,445	ADAM5, ADAM3A
nsv4365134	copy number variation	6	nstd173	human	GRCh37 chr8: 102,954,989-102,975,180 , GRCh38.p12 chr8: 101,942,761-101,962,952	NCALD,
nsv4385380	copy number variation	1	nstd173	human	GRCh37 chr3: 100,336,444-100,420,319 , GRCh38.p12 chr3: 100,617,600-100,701,475	ADGRG7, GMFBP1
nsv4381557	copy number variation	18	nstd173	human	GRCh37 chr19: 55,298,579-55,324,041 , GRCh38.p12 chr19\|NT_187693.1: 769,693-795,155	KIR2DL4, KIR3DP1
nsv4375714	copy number variation	376	nstd173	human	GRCh37 chr4: 69,435,889-69,485,978 , GRCh38.p12 chr4: 68,570,171-68,620,260	UGT2B17, LOC100132651, 1 more genes
nsv4382508	copy number variation	18	nstd173	human	GRCh37 chr16: 15,054,346-15,126,890 , GRCh38.p12 chr16: 14,960,489-15,033,033	MIR1972-1, LOC728138, 1 more genes
nsv4385949	copy number variation	1	nstd173	human	GRCh37 chrX: 148,884,729-148,992,997 , GRCh38.p12 chrX: 149,803,067-149,864,197	DUTP4, MAGEA7P, 1 more genes
nsv4373610	copy number variation	1	nstd173	human	GRCh37 chrX: 148,998,596-149,028,747 , GRCh38.p12 chrX: 149,869,796-149,899,974	MAGEA8-AS1, MAGEA8, 1 more genes
nsv4376002	copy number variation	4	nstd173	human	GRCh37 chr1: 248,688,587-248,795,288 , GRCh38.p12 chr1: 248,525,286-248,631,987	OR2AS1P, OR2T34, 4 more genes
nsv4381410	copy number variation	1	nstd173	human	GRCh37 chr5: 180,374,523-180,445,208 , GRCh38.p12 chr5: 180,947,523-181,018,208	BTNL8, ARPP19P1, 4 more genes
nsv4379829	copy number variation	1	nstd173	human	GRCh37 chr14: 22,591,821-22,941,375 , GRCh38.p12 chr14: 22,123,863-22,472,385	TRAV27, TRAV33, 33 more genes
nsv4386339	copy number variation	89	nstd173	human	GRCh37 chr16: 34,466,475-34,755,828 , GRCh38.p12 chr16: 35,232,104-35,521,457	LOC105371204, C2orf69P4, 26 more genes
nsv4387566	copy number variation	315	nstd173	human	GRCh37 chr2: 34,701,655-34,727,784 , GRCh38.p12 chr2: 34,476,588-34,502,717	0

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Number of Variants: 20

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