2-1547-003 AND nstd173 - dbVar - NCBI

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4378764	copy number variation	65	nstd173	human		GRCh37 chr10: 124,358,181-124,382,030 , GRCh38.p12 chr10: 122,598,665-122,622,514	DMBT1
nsv4373295	copy number variation	124	nstd173	human		GRCh37 chr13: 69,248,299-69,268,719 , GRCh38.p12 chr13: 68,674,167-68,694,587	RN7SL761P
nsv4368823	copy number variation	1	nstd173	human		GRCh37 chr2: 215,095,804-215,122,791 , GRCh38.p12 chr2: 214,231,080-214,258,067	SPAG16
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
nsv4372080	copy number variation	569	nstd173	human		GRCh37 chr1: 72,762,663-72,812,440 , GRCh38.p12 chr1: 72,296,980-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,982	RPL31P12, LOC105378797
nsv4381578	copy number variation	2	nstd173	human		GRCh37 chr4: 129,774,328-129,933,968 , GRCh38.p12 chr4: 128,853,173-129,012,813	JADE1, SCLT1
nsv4387022	copy number variation	27	nstd173	human		GRCh37 chr1: 1,616,990-1,672,591 , GRCh38.p12 chr1: 1,685,551-1,741,152	SLC35E2B, LOC100129381, 3 more genes
nsv4384776	copy number variation	87	nstd173	human		GRCh37 chr19: 52,131,800-52,154,905 , GRCh38.p12 chr19: 51,628,547-51,651,652	SIGLEC5, SIGLEC14, 1 more genes
nsv4382988	copy number variation	1	nstd173	human		GRCh37 chr19: 56,706,501-56,758,781 , GRCh38.p12 chr19: 56,195,132-56,247,412	ZSCAN5DP, RPL13P13, 3 more genes
nsv4387472	copy number variation	14	nstd173	human		GRCh37 chr5: 180,378,754-180,407,217 , GRCh38.p12 chr5: 180,951,754-180,980,217	ARPP19P1, BTNL8, 2 more genes
nsv4387125	copy number variation	432	nstd173	human		GRCh37 chr2: 35,967,123-35,997,473 , GRCh38.p12 chr2: 35,742,057-35,772,407	0
nsv4382474	copy number variation	59	nstd173	human		GRCh37 chr17: 44,188,310-44,784,639 , GRCh38.p12 chr17: 46,110,944-46,707,273 , GRCh38.p12 chr17\|NT_187663.1: 813,043-1,226,699	RN7SL199P, ARL17A, 14 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

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