161744 AND nstd173 - dbVar - NCBI

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4387213	copy number variation	434	nstd173	human		GRCh37 chr4: 34,779,032-34,824,730 , GRCh38.p12 chr4: 34,777,410-34,823,108 , GRCh38.p12 chr4\|NW_003315915.1: 269,739-315,437	LOC105378262
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
nsv4376978	copy number variation	1	nstd173	human		GRCh37 chr9: 2,234,701-2,364,269 , GRCh38.p12 chr9: 2,234,701-2,364,269	LOC105375955, LOC107987043
nsv4371533	copy number variation	83	nstd173	human		GRCh37 chr1: 72,762,663-72,811,135 , GRCh38.p12 chr1: 72,296,980-72,345,452 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-66,677	RPL31P12, LOC105378797
nsv4366434	copy number variation	1	nstd173	human		GRCh37 chr3: 35,800,767-35,941,198 , GRCh38.p12 chr3: 35,759,275-35,899,706	RPL36AP17, ARPP21
nsv4382857	copy number variation	37	nstd173	human		GRCh37 chr12: 8,558,475-8,584,671 , GRCh38.p12 chr12: 8,405,879-8,432,075	OR7E148P, OR7E140P
nsv4383228	copy number variation	5	nstd173	human		GRCh37 chr11: 134,348,704-134,719,069 , GRCh38.p12 chr11: 134,478,810-134,849,175	LINC02714, LOC105369583, 2 more genes
nsv4386129	copy number variation	134	nstd173	human		GRCh37 chr17: 34,439,977-34,477,480 , GRCh38.p12 chr17: 36,112,584-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 66,681-104,195 , GRCh38.p12 chr17\|NT_187614.1: 347,505-385,008	LOC101927369, LOC100419980, 2 more genes
nsv4373711	copy number variation	238	nstd173	human		GRCh37 chr14: 74,001,111-74,031,034 , GRCh38.p12 chr14: 73,534,407-73,564,330	NT5CP2, HEATR4, 1 more genes
nsv4382222	copy number variation	125	nstd173	human		GRCh37 chr1: 248,688,587-248,795,289 , GRCh38.p12 chr1: 248,525,286-248,631,988	OR2AS1P, OR2T34, 4 more genes
nsv4379987	copy number variation	105	nstd173	human		GRCh37 chr14: 86,284,754-86,309,385 , GRCh38.p12 chr14: 85,818,410-85,843,041	0
nsv4384187	copy number variation	1	nstd173	human		GRCh37 chr1: 55,106,105-55,283,311 , GRCh38.p12 chr1: 54,640,432-54,817,638	TTC4, PARS2, 4 more genes
nsv4366704	copy number variation	18	nstd173	human		GRCh37 chr10: 135,252,179-135,377,265 , GRCh38.p12 chr10: 133,438,675-133,563,761	, CYP2E1, 5 more genes
nsv4375900	copy number variation	25	nstd173	human		GRCh37 chr14: 22,480,324-22,974,280 , GRCh38.p12 chr14: 22,012,085-22,505,293	TRAJ37, TRAJ45, 68 more genes
nsv4378546	copy number variation	1	nstd173	human		GRCh37 chr14: 102,888,825-103,225,212 , GRCh38.p12 chr14: 102,422,488-102,758,875	LOC105370679, ANKRD9, 8 more genes
nsv4370882	copy number variation	1	nstd173	human		GRCh37 chr7: 142,260,874-142,499,697 , GRCh38.p12 chr7: 142,618,685-142,802,013 , GRCh38.p12 chr7\|NT_187562.1: 656,734-781,128	TRB, TRBV21-1, 37 more genes
nsv4386781	copy number variation	19	nstd173	human		GRCh37 chr7: 38,293,950-38,370,792 , GRCh38.p12 chr7: 38,254,349-38,331,191	TRGJP2, LOC103689914, 13 more genes

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161744 AND nstd173 (18)
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