2-1593-001 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
nsv4382812	copy number variation	15	nstd173	human		GRCh37 chr18: 1,725,758-1,841,469 , GRCh38.p12 chr18: 1,725,757-1,841,468 , GRCh38.p12 chr18\|NW_019805503.1: 1-119,817	LOC105371959
nsv4384985	copy number variation	1	nstd173	human		GRCh37 chr12: 86,914,268-87,031,785 , GRCh38.p12 chr12: 86,520,491-86,638,008	MGAT4C
nsv4379023	copy number variation	4	nstd173	human		GRCh37 chr1: 60,004,764-60,052,053 , GRCh38.p12 chr1: 59,539,092-59,586,381	FGGY
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
nsv4380479	copy number variation	1	nstd173	human		GRCh37 chr4: 18,539,084-18,562,949 , GRCh38.p12 chr4: 18,537,461-18,561,326	LOC105374510
nsv4382964	copy number variation	1	nstd173	human		GRCh37 chr7: 112,442,234-112,476,756 , GRCh38.p12 chr7: 112,802,179-112,836,701	BMT2
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
nsv4365156	copy number variation	1	nstd173	human		GRCh37 chr5: 32,109,542-32,158,470 , GRCh38.p12 chr5: 32,109,436-32,158,364	PDZD2, GOLPH3
nsv4371149	copy number variation	17	nstd173	human		GRCh37 chr17: 44,198,096-44,292,754 , GRCh38.p12 chr17: 46,120,730-46,215,388 , GRCh38.p12 chr17\|NT_187663.1: 822,827-917,561	KANSL1, KANSL1-AS1, 1 more genes
nsv4370631	copy number variation	136	nstd173	human		GRCh37 chr11: 5,787,573-5,809,230 , GRCh38.p12 chr11: 5,766,343-5,788,000	OR52N1, OR56B2P, 1 more genes
nsv4382082	copy number variation	609	nstd173	human		GRCh37 chr11: 55,374,019-55,442,305 , GRCh38.p12 chr11: 55,606,543-55,674,829	OR4C6, OR4P4, 2 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
nsv4380971	copy number variation	213	nstd173	human		GRCh37 chr6: 29,841,021-29,936,041 , GRCh38.p12 chr6: 29,873,244-29,968,264	HLA-H, HCG4P4, 12 more genes
nsv4383655	copy number variation	30	nstd173	human		GRCh37 chr11: 54,965,375-55,009,349 , GRCh38.p12 chr11: 55,197,899-55,241,873	0
nsv4381531	copy number variation	237	nstd173	human		GRCh37 chr2: 34,701,643-34,737,163 , GRCh38.p12 chr2: 34,476,576-34,512,096	0
nsv4382392	copy number variation	421	nstd173	human		GRCh37 chr3: 65,185,849-65,210,375 , GRCh38.p12 chr3: 65,200,174-65,224,700	0
nsv4367615	copy number variation	8	nstd173	human		GRCh37 chr14: 106,072,251-106,223,587 , GRCh38.p12 chr14: 105,605,914-105,757,250 , GRCh38.p12 chr14\|NT_187600.1: 73,683-225,019	MIR8071-2, IGHG1, 13 more genes
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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