2-1337-004 AND nstd173 - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4367014	copy number variation	172	nstd173	human		GRCh37 chr6: 78,969,104-79,035,184 , GRCh38.p12 chr6: 78,259,387-78,325,467	LOC105377865
nsv4365889	copy number variation	2	nstd173	human		GRCh37 chr4: 104,802,331-104,852,661 , GRCh38.p12 chr4: 103,881,174-103,931,504	RNU6-635P
nsv4368568	copy number variation	177	nstd173	human		GRCh37 chr14: 41,610,556-41,657,457 , GRCh38.p12 chr14: 41,141,353-41,188,254	LINC02315
nsv4379737	copy number variation	349	nstd173	human		GRCh37 chr1: 169,216,099-169,241,765 , GRCh38.p12 chr1: 169,246,861-169,272,527	NME7
nsv4371805	copy number variation	282	nstd173	human		GRCh37 chr11: 18,941,197-18,961,975 , GRCh38.p12 chr11: 18,919,650-18,940,428	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
nsv4375212	copy number variation	547	nstd173	human		GRCh37 chr1: 72,762,663-72,811,904 , GRCh38.p12 chr1: 72,296,980-72,346,221 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,446	RPL31P12, LOC105378797
nsv4388035	copy number variation	283	nstd173	human		GRCh37 chr1: 104,109,088-104,132,506 , GRCh38.p12 chr1: 103,566,466-103,589,884	AMY2B, ACTG1P4
nsv4380515	copy number variation	77	nstd173	human		GRCh37 chr12: 8,558,475-8,594,982 , GRCh38.p12 chr12: 8,405,879-8,442,386	OR7E148P, OR7E149P, 1 more genes
nsv4378128	copy number variation	463	nstd173	human		GRCh37 chr11: 51,337,076-51,376,963 , GRCh38.p12 chr11: 54,742,317-54,782,204	0
nsv4384501	copy number variation	242	nstd173	human		GRCh37 chr16: 19,945,795-19,965,942 , GRCh38.p12 chr16: 19,934,473-19,954,620	0
nsv4370946	copy number variation	301	nstd173	human		GRCh37 chr16: 34,466,691-34,755,828 , GRCh38.p12 chr16: 35,232,320-35,521,457	RARRES2P7, AGGF1P9, 26 more genes

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