M2422 AND nstd157 - 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
nsv3318384	copy number variation	1	nstd157	human		GRCh37 chr8: 89,688,978-89,714,401 , GRCh38.p12 chr8: 88,676,749-88,702,172	LOC105375630
nsv3318727	copy number variation	1	nstd157	human		GRCh37 chr4: 12,587,401-12,606,923 , GRCh38.p12 chr4: 12,585,777-12,605,299	LOC105374492
nsv3318914	copy number variation	27	nstd157	human		GRCh37 chr20: 52,647,631-52,656,535 , GRCh38.p12 chr20: 54,031,092-54,039,996	BCAS1
nsv3318348	copy number variation	10	nstd157	human		GRCh37 chr11: 85,263,724-85,271,049 , GRCh38.p12 chr11: 85,552,680-85,560,005	DLG2
nsv3317580	copy number variation	32	nstd157	human		GRCh37 chr7: 156,387,296-156,394,307 , GRCh38.p12 chr7: 156,594,602-156,601,613	RNF32-DT
nsv3317683	copy number variation	3	nstd157	human		GRCh37 chr17: 77,365,704-77,391,145 , GRCh38.p12 chr17: 79,369,622-79,395,063	RBFOX3
nsv3318495	copy number variation	28	nstd157	human		GRCh37 chr11: 18,949,220-18,961,743 , GRCh38.p12 chr11: 18,927,673-18,940,196	MRGPRX1
nsv3317651	copy number variation	14	nstd157	human		GRCh37 chr3: 195,458,723-195,467,820 , GRCh38.p12 chr3: 195,731,852-195,740,949 , GRCh38.p12 chr3\|NT_187678.1: 55,095-64,192 , GRCh38.p12 chr3\|NT_187688.1: 53,782-62,847 , GRCh38.p12 chr3\|NT_187689.1: 102,349-111,446 , GRCh38.p12 chr3\|NT_187690.1: 53,786-62,854 , GRCh38.p12 chr3\|NT_187691.1: 53,898-63,024 , GRCh38.p12 chr3\|NT_187532.1: 102,349-111,446 , GRCh38.p12 chr3\|NT_187649.1: 53,782-62,847	MUC20
nsv3317736	copy number variation	10	nstd157	human		GRCh38.p12 chr14: 85,991,608-86,022,749 , GRCh37 chr14: 86,457,952-86,489,093	LINC02328, LINC02316
nsv3317142	copy number variation	9	nstd157	human		GRCh37 chr5: 32,106,628-32,164,826 , GRCh38.p12 chr5: 32,106,522-32,164,720	PDZD2, GOLPH3
nsv3317855	copy number variation	1	nstd157	human		GRCh37 chr3: 95,973-127,551 , GRCh38.p12 chr3: 54,290-85,868	LOC105376921, LOC107986040
nsv3318116	copy number variation	1	nstd157	human		GRCh38.p12 chr2: 32,912,679-33,085,827 , GRCh37 chr2: 33,137,746-33,310,894	LTBP1, LINC00486, 1 more genes
nsv3318457	copy number variation	10	nstd157	human		GRCh38.p12 chr6: 266,035-379,638 , GRCh37 chr6: 266,035-379,638	DUSP22, , 1 more genes
nsv3318745	copy number variation	44	nstd157	human		GRCh37 chr17: 34,438,753-34,483,342 , GRCh38.p12 chr17: 36,111,360-36,155,969 , GRCh38.p12 chr17\|NT_187661.1: 65,457-110,066 , GRCh38.p12 chr17\|NT_187614.1: 346,281-390,870	LOC100419980, LOC101927369, 2 more genes
nsv3317469	copy number variation	35	nstd157	human		GRCh37 chr3: 65,189,366-65,214,533 , GRCh38.p12 chr3: 65,203,691-65,228,858	0
nsv3317844	copy number variation	7	nstd157	human		GRCh37 chr2: 165,850,456-165,864,123 , GRCh38.p12 chr2: 164,993,946-165,007,613	0
nsv3318836	copy number variation	1	nstd157	human		GRCh37 chr9: 7,226,519-7,234,019 , GRCh38.p12 chr9: 7,226,519-7,234,019	0
nsv3318657	copy number variation	1	nstd157	human		GRCh38.p12 chr1: 40,880,756-40,915,899 , GRCh37 chr1: 41,346,428-41,381,571	0
nsv3318389	copy number variation	4	nstd157	human		GRCh38.p12 chr8: 26,476,982-26,485,915 , GRCh37 chr8: 26,334,498-26,343,431	0

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