1-0756-003 AND nstd173 - dbVar - NCBI

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Items: 18

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4371180	copy number variation	3	nstd173	human		GRCh37 chr9: 11,782,269-12,071,041 , GRCh38.p12 chr9: 11,782,269-12,071,041	LOC101929446
nsv4372152	copy number variation	236	nstd173	human		GRCh37 chr6: 78,969,092-79,035,184 , GRCh38.p12 chr6: 78,259,375-78,325,467	LOC105377865
nsv4381001	copy number variation	3	nstd173	human		GRCh37 chr3: 4,114,722-4,162,527 , GRCh38.p12 chr3: 4,073,038-4,120,843	SUMF1
nsv4386677	copy number variation	1	nstd173	human		GRCh37 chr9: 37,051,138-37,092,433 , GRCh38.p12 chr9: 37,051,141-37,092,436	EBLN3P
nsv4379109	copy number variation	1337	nstd173	human		GRCh37 chr20: 1,560,774-1,597,997 , GRCh38.p12 chr20: 1,580,128-1,617,351	SIRPB1
nsv4386429	copy number variation	124	nstd173	human		GRCh37 chr13: 57,758,276-57,778,379 , GRCh38.p12 chr13: 57,184,142-57,204,245	MTCO2P3
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
nsv4375250	copy number variation	37	nstd173	human		GRCh37 chr10: 47,588,964-47,609,552 , GRCh38.p12 chr10: 46,217,728-46,238,316	AHCYP1, ANTXRLP1
nsv4377457	copy number variation	1	nstd173	human		GRCh37 chr1: 199,715,370-199,927,177 , GRCh38.p12 chr1: 199,746,242-199,958,049	LOC107985114, LOC100422076, 3 more genes
nsv4373389	copy number variation	2	nstd173	human		GRCh37 chr19: 53,311,563-53,366,906 , GRCh38.p12 chr19: 52,808,310-52,863,653	PABPN1P2, ZNF468, 2 more genes
nsv4366691	copy number variation	623	nstd173	human		GRCh37 chr4: 69,435,901-69,485,978 , GRCh38.p12 chr4: 68,570,183-68,620,260	UGT2B17, LOC100422402, 1 more genes
nsv4388322	copy number variation	1	nstd173	human		GRCh37 chr11: 55,403,570-55,442,196 , GRCh38.p12 chr11: 55,636,094-55,674,720	OR4C6, OR4V1P, 2 more genes
nsv4374133	copy number variation	39	nstd173	human		GRCh37 chr3: 175,883,703-175,916,315 , GRCh38.p12 chr3: 176,165,915-176,198,527 , GRCh38.p12 chr3\|NW_019805488.1: 50,426-83,038	0
nsv4380160	copy number variation	62	nstd173	human		GRCh37 chr6: 110,394,605-110,415,415 , GRCh38.p12 chr6: 110,073,402-110,094,212	0
nsv4375393	copy number variation	59	nstd173	human		GRCh37 chr17: 36,283,807-36,410,559 , GRCh38.p12 chr17\|NT_187614.1: 2,162,872-2,289,624	NPEPPSP1, TBC1D3, 6 more genes
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

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