1-0898-003 AND nstd173 - dbVar - NCBI

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Items: 19

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Number of Variants: 19

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
nsv4376921	copy number variation	59	nstd173	human		GRCh37 chr2: 98,118,199-98,161,960 , GRCh38.p12 chr2: 97,501,736-97,545,497	ANKRD36B
nsv4376212	copy number variation	5	nstd173	human		GRCh37 chr20: 1,557,177-1,590,244 , GRCh38.p12 chr20: 1,576,531-1,609,598	SIRPB1
nsv4379306	copy number variation	3	nstd173	human		GRCh37 chr13: 69,242,149-69,269,380 , GRCh38.p12 chr13: 68,668,017-68,695,248	RN7SL761P
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
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
nsv4381970	copy number variation	2	nstd173	human		GRCh37 chr12: 11,496,820-11,560,919 , GRCh38.p12 chr12: 11,343,886-11,407,985 , GRCh38.p12 chr12\|NT_187658.1: 538,849-572,349	PRB2, PRB1
nsv4367066	copy number variation	60	nstd173	human		GRCh37 chr14: 86,460,915-86,494,554 , GRCh38.p12 chr14: 85,994,571-86,028,210	LINC02316, LINC02328
nsv4374105	copy number variation	16	nstd173	human		GRCh37 chr11: 4,967,363-4,991,060 , GRCh38.p12 chr11: 4,946,133-4,969,830	OR51A4, OR51A2
nsv4376860	copy number variation	7	nstd173	human		GRCh37 chr17: 43,570,226-43,655,331 , GRCh38.p12 chr17: 45,492,860-45,577,965 , GRCh38.p12 chr17\|NT_187663.1: 183,015-280,104	LOC102724345, LOC112267925, 4 more genes
nsv4367271	copy number variation	561	nstd173	human		GRCh37 chr11: 5,786,020-5,809,230 , GRCh38.p12 chr11: 5,764,790-5,788,000	OR56B2P, OR52N1, 1 more genes
nsv4371881	copy number variation	52	nstd173	human		GRCh37 chr17: 44,212,836-44,292,754 , GRCh38.p12 chr17: 46,135,470-46,215,388 , GRCh38.p12 chr17\|NT_187663.1: 837,577-917,561	KANSL1, KANSL1-AS1, 1 more genes
nsv4371226	copy number variation	2	nstd173	human		GRCh37 chr6: 258,252-294,316 , GRCh38.p12 chr6: 258,252-294,316	DUSP22, , 1 more genes
nsv4368821	copy number variation	1373	nstd173	human		GRCh37 chr22: 24,353,749-24,385,040 , GRCh38.p12 chr22\|NT_187633.1: 247,924-279,215	LOC391322, GSTTP2, 3 more genes
nsv4369919	copy number variation	116	nstd173	human		GRCh37 chr14: 106,530,472-106,667,035 , GRCh38.p12 chr14: 106,074,229-106,210,392 , GRCh38.p12 chr14\|NT_187600.1: 541,998-678,161	IGHV1-18, IGHV3-20, 17 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
nsv4368660	copy number variation	868	nstd173	human		GRCh37 chr6: 103,738,197-103,759,824 , GRCh38.p12 chr6: 103,290,322-103,311,949	0
nsv4369274	copy number variation	262	nstd173	human		GRCh37 chr2: 35,976,209-35,997,473 , GRCh38.p12 chr2: 35,751,143-35,772,407	0
nsv4381254	copy number variation	14	nstd173	human		GRCh37 chr17: 36,300,466-36,410,559 , GRCh38.p12 chr17\|NT_187614.1: 2,179,531-2,289,624	TBC1D3, RNA5SP526, 4 more genes

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