"nstd168"[study] AND "intrachromosomal translocation"[variant_type] - dbVar - NCBI

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Items: 11

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3971590	translocation	1	nstd168	human		GRCh37.p13 chr1\|NW_003871055.3: 3,096,953-3,096,953 , GRCh37.p13 chr1\|NW_003871056.3: 269,372-269,372 , GRCh38 chr1: 146,281,540-146,281,540 , GRCh38 chr1: 120,197,798-120,197,798 , GRCh37.p13 chr1: 145,156,580-145,156,580	LOC100996723
nsv3971585	translocation	1	nstd168	human		GRCh38 chr16: 90,088,131-90,088,131 , GRCh38 chr16: 47,295-47,295 , GRCh37.p13 chr16: 97,295-97,295 , GRCh37.p13 chr16: 90,154,539-90,154,539	POLR3K
nsv3971583	translocation	1	nstd168	human		GRCh38 chr15: 20,582,646-20,582,646 , GRCh38 chr15: 28,522,118-28,522,118 , GRCh37.p13 chr15: 20,787,970-20,787,970 , GRCh37.p13 chr15: 28,767,264-28,767,264	GOLGA8G
nsv3971589	translocation	1	nstd168	human		GRCh38 chr1: 144,008,448-144,008,448 , GRCh38 chr1: 206,280,786-206,280,786 , GRCh37.p13 chr1\|NW_003871057.1: 271,640-271,640 , GRCh37.p13 chr1\|NW_003871055.3: 823,861-823,861	SRGAP2, SRGAP2D
nsv3971588	translocation	1	nstd168	human		GRCh38 chr1: 144,898,888-144,898,888 , GRCh38 chr1: 206,415,604-206,415,604 , GRCh37.p13 chr1: 206,588,964-206,588,964 , GRCh37.p13 chr1\|NW_003871057.1: 406,458-406,458 , GRCh37.p13 chr1\|NW_003871055.3: 1,714,301-1,714,301	SRGAP2, SRGAP2B
nsv3971584	translocation	1	nstd168	human		GRCh38 chr10: 87,398,144-87,398,144 , GRCh38 chr10: 79,869,602-79,869,602 , GRCh37.p13 chr10: 81,629,358-81,629,358 , GRCh37.p13 chr10: 89,157,901-89,157,901	CTSLP6, FAM245A
nsv3971576	translocation	1	nstd168	human		GRCh38 chr9: 41,172,434-41,172,434 , GRCh38 chr9: 64,018,990-64,018,990 , GRCh37.p13 chr9: 69,245,663-69,245,663 , GRCh37.p13 chr22\|NT_113961.1: 50,543-50,543	ZNG1F, FLJ43315
nsv3971572	translocation	1	nstd168	human		GRCh38 chr1: 144,886,854-144,886,854 , GRCh38 chr1: 121,403,752-121,403,752 , GRCh37.p13 chr1: 121,145,612-121,145,612 , GRCh37.p13 chr1\|NW_003871056.3: 1,475,326-1,475,326 , GRCh37.p13 chr1\|NW_003871055.3: 1,702,267-1,702,267	SRGAP2B, LINC02798
nsv3971566	translocation	1	nstd168	human		GRCh38 chr1: 121,376,774-121,376,774 , GRCh38 chr1: 206,415,604-206,415,604 , GRCh37.p13 chr1: 121,118,636-121,118,636 , GRCh37.p13 chr1: 206,588,964-206,588,964 , GRCh37.p13 chr1\|NW_003871057.1: 406,458-406,458 , GRCh37.p13 chr1\|NW_003871056.3: 1,448,348-1,448,348	SRGAP2, SRGAP2C, 1 more genes
nsv3971556	translocation	1	nstd168	human		GRCh37.p13 chr5: 21,496,760-21,496,760 , GRCh37.p13 chr5: 34,194,079-34,194,079 , GRCh38 chr5: 21,496,651-21,496,651 , GRCh38 chr5: 34,193,974-34,193,974	C1QTNF3, LOC646652, 1 more genes
nsv3971586	translocation	1	nstd168	human		GRCh37.p13 chr1\|NW_003871055.3: 6,640,384-6,640,384 , GRCh37.p13 chr1\|NW_003871056.3: 1,223,360-1,223,360 , GRCh38 chr1: 121,151,786-121,151,786 , GRCh38 chr1: 149,824,971-149,824,971 , GRCh37.p13 chr1: 120,871,535-120,871,535 , GRCh37.p13 chr1: 149,796,524-149,796,524	0

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"nstd168"[study] AND "intrachromosomal translocation"[variant_typ... (12)
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