2-0285-001 AND nstd173 - dbVar - NCBI

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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
nsv4380512	copy number variation	13	nstd173	human		GRCh37 chr3: 89,386,935-89,419,375 , GRCh38.p12 chr3: 89,337,785-89,370,225	EPHA3
nsv4367137	copy number variation	9	nstd173	human		GRCh37 chr2: 98,141,311-98,162,188 , GRCh38.p12 chr2: 97,524,848-97,545,725	ANKRD36B
nsv4367079	copy number variation	1	nstd173	human		GRCh37 chr11: 50,297,005-51,205,141 , GRCh38.p12 chr11: 50,337,834-50,821,348	LOC646813, LINC02750
nsv4386160	copy number variation	1	nstd173	human		GRCh37 chr10: 62,399,144-62,475,891 , GRCh38.p12 chr10: 60,639,386-60,716,133	ANK3, ARL4AP1
nsv4369217	copy number variation	2	nstd173	human		GRCh37 chr11: 59,127,460-59,227,430 , GRCh38.p12 chr11: 59,359,987-59,459,957	OR5A1, OR5A2, 3 more genes
nsv4379472	copy number variation	106	nstd173	human		GRCh37 chr6: 257,061-294,923 , GRCh38.p12 chr6: 257,061-294,923	DUSP22, , 1 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
nsv4377875	copy number variation	73	nstd173	human		GRCh37 chr5: 180,375,302-180,430,797 , GRCh38.p12 chr5: 180,948,302-181,003,797	BTNL8, BTNL3, 3 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
nsv4388533	copy number variation	2	nstd173	human		GRCh37 chr15: 43,888,479-43,984,930 , GRCh38.p12 chr15: 43,596,281-43,692,732	CKMT1B, CATSPER2, 7 more genes
nsv4385955	copy number variation	154	nstd173	human		GRCh37 chr3: 162,521,309-162,626,676 , GRCh38.p12 chr3: 162,803,521-162,908,888	0
nsv4370779	copy number variation	156	nstd173	human		GRCh37 chr5: 8,702,522-8,750,244 , GRCh38.p12 chr5: 8,702,410-8,750,132	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
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
nsv4385529	copy number variation	179	nstd173	human		GRCh37 chr14: 106,525,299-106,692,891 , GRCh38.p12 chr14: 106,069,054-106,236,281 , GRCh38.p12 chr14\|NT_187600.1: 536,823-704,050	IGHVIII-13-1, IGHV1-18, 19 more genes
nsv4372776	copy number variation	31	nstd173	human		GRCh37 chr11: 51,337,076-51,376,963 , GRCh38.p12 chr11: 54,742,317-54,782,204	0
nsv4383835	copy number variation	2	nstd173	human		GRCh37 chr2: 5,478,633-5,511,339 , GRCh38.p12 chr2: 5,338,500-5,371,206	0

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