200018 AND nstd173 - dbVar - NCBI

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4368858	copy number variation	16	nstd173	human		GRCh37 chr6: 78,969,104-79,041,720 , GRCh38.p12 chr6: 78,259,387-78,332,003	LOC105377865
nsv4387761	copy number variation	17	nstd173	human		GRCh37 chr10: 124,344,096-124,382,030 , GRCh38.p12 chr10: 122,584,580-122,622,514	DMBT1
nsv4384133	copy number variation	106	nstd173	human		GRCh37 chr1: 169,216,044-169,241,765 , GRCh38.p12 chr1: 169,246,806-169,272,527	NME7
nsv4367576	copy number variation	72	nstd173	human		GRCh37 chr8: 15,400,912-15,423,270 , GRCh38.p12 chr8: 15,543,403-15,565,761	TUSC3
nsv4376485	copy number variation	50	nstd173	human		GRCh37 chr3: 173,239,853-173,300,180 , GRCh38.p12 chr3: 173,522,063-173,582,390	NLGN1
nsv4385455	copy number variation	190	nstd173	human		GRCh37 chr20: 1,557,177-1,597,997 , GRCh38.p12 chr20: 1,576,531-1,617,351	SIRPB1
nsv4387002	copy number variation	71	nstd173	human		GRCh37 chr3: 128,380,595-128,412,377 , GRCh38.p12 chr3: 128,661,752-128,693,534	POU5F1P6
nsv4371805	copy number variation	282	nstd173	human		GRCh37 chr11: 18,941,197-18,961,975 , GRCh38.p12 chr11: 18,919,650-18,940,428	MRGPRX1
nsv4372080	copy number variation	569	nstd173	human		GRCh37 chr1: 72,762,663-72,812,440 , GRCh38.p12 chr1: 72,296,980-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,982	RPL31P12, LOC105378797
nsv4365236	copy number variation	23	nstd173	human		GRCh37 chr6: 257,049-381,137 , GRCh38.p12 chr6: 257,049-381,137	, , 1 more genes
nsv4380649	copy number variation	59	nstd173	human		GRCh37 chr4: 69,366,693-69,485,978 , GRCh38.p12 chr4: 68,500,975-68,620,260	LOC100132651, UGT2B29P, 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
nsv4367001	copy number variation	197	nstd173	human		GRCh37 chr14: 74,001,111-74,024,031 , GRCh38.p12 chr14: 73,534,407-73,557,327	NT5CP2, ACOT1, 1 more genes
nsv4375644	copy number variation	145	nstd173	human		GRCh37 chr22: 25,656,238-25,922,334 , GRCh38.p12 chr22: 25,260,271-25,526,367	CRYBB2P1, IGLL3P, 4 more genes
nsv4371199	copy number variation	115	nstd173	human		GRCh37 chr2: 52,738,983-52,790,493 , GRCh38.p12 chr2: 52,511,845-52,563,355	0
nsv4369166	copy number variation	31	nstd173	human		GRCh37 chr8: 13,611,631-13,652,975 , GRCh38.p12 chr8: 13,754,122-13,795,466	0
nsv4380168	copy number variation	295	nstd173	human		GRCh37 chr17: 44,187,492-44,784,639 , GRCh38.p12 chr17: 46,110,126-46,707,273 , GRCh38.p12 chr17\|NT_187663.1: 812,225-1,226,699	MAPK8IP1P1, DND1P2, 14 more genes
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

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