2-1235-003 AND nstd173 - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4379129	copy number variation	5	nstd173	human		GRCh37 chr8: 137,677,896-137,862,600 , GRCh38.p12 chr8: 136,665,653-136,850,357	LINC02055
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
nsv4376284	copy number variation	379	nstd173	human		GRCh37 chr14: 41,608,616-41,657,457 , GRCh38.p12 chr14: 41,139,413-41,188,254	LINC02315
nsv4380792	copy number variation	37	nstd173	human		GRCh37 chr1: 72,773,260-72,811,904 , GRCh38.p12 chr1: 72,307,577-72,346,221 , GRCh38.p12 chr1\|NW_018654707.1: 19,844-67,446	LOC105378797
nsv4386779	copy number variation	33	nstd173	human		GRCh37 chr7: 141,755,372-141,799,117 , GRCh38.p12 chr7: 142,055,572-142,099,317 , GRCh38.p12 chr7\|NT_187562.1: 17,452-61,197	MGAM
nsv4368763	copy number variation	6	nstd173	human		GRCh37 chr22: 28,587,121-28,607,657 , GRCh38.p12 chr22: 28,191,133-28,211,669	TTC28
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
nsv4374985	copy number variation	188	nstd173	human		GRCh37 chr14: 73,995,761-74,024,031 , GRCh38.p12 chr14: 73,529,057-73,557,327	ACOT1, NT5CP2, 1 more genes
nsv4370277	copy number variation	687	nstd173	human		GRCh37 chr5: 180,378,754-180,430,789 , GRCh38.p12 chr5: 180,951,754-181,003,789	BTNL8, ARPP19P1, 3 more genes
nsv4376452	copy number variation	337	nstd173	human		GRCh37 chr17: 34,437,494-34,477,480 , GRCh38.p12 chr17: 36,110,101-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 64,198-104,195 , GRCh38.p12 chr17\|NT_187614.1: 345,022-385,008	LOC101927369, LOC107985055, 3 more genes
nsv4386828	copy number variation	67	nstd173	human		GRCh37 chr19: 20,596,118-20,716,388 , GRCh38.p12 chr19: 20,413,312-20,533,582	ZNF826P, ZNF737, 4 more genes
nsv4374879	copy number variation	3	nstd173	human		GRCh37 chr9: 11,988,678-12,091,322 , GRCh38.p12 chr9: 11,988,678-12,091,322	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
nsv4369327	copy number variation	2	nstd173	human		GRCh37 chr4: 109,385,403-109,408,513 , GRCh38.p12 chr4: 108,464,247-108,487,357	0
nsv4379278	copy number variation	2	nstd173	human		GRCh37 chr15: 81,988,453-82,089,070 , GRCh38.p12 chr15: 81,696,112-81,796,729	0
nsv4372589	copy number variation	741	nstd173	human		GRCh37 chr14: 106,530,472-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

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