HGDP01079 AND nstd54 - dbVar - NCBI

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Number of Variants: 8

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv603867	copy number variation	617	nstd54	human		NCBI36 chr6: 79,029,920-79,088,461 , GRCh37.p13 chr6: 78,973,201-79,031,742 , GRCh38.p12 chr6: 78,263,484-78,322,025	LOC105377865
nsv594110	copy number variation	1	nstd54	human		NCBI36 chr4: 45,174,831-45,290,002 , GRCh37.p13 chr4: 45,480,074-45,595,245 , GRCh38.p12 chr4: 45,478,057-45,593,228	RNU6-931P
nsv591409	copy number variation	1	nstd54	human		NCBI36 chr3: 124,151,847-124,172,088 , GRCh37.p13 chr3: 122,669,157-122,689,398 , GRCh38.p12 chr3: 122,950,310-122,970,551	SEMA5B,
nsv586557	copy number variation	1	nstd54	human		NCBI36 chr20: 61,256,104-61,337,899 , GRCh37.p13 chr20: 61,785,659-61,867,454 , GRCh38.p12 chr20: 63,154,307-63,236,102	YTHDF1, BIRC7, 1 more genes
nsv586129	copy number variation	6	nstd54	human		NCBI36 chr20: 43,788,634-43,811,984 , GRCh37.p13 chr20: 44,355,220-44,378,577 , GRCh38.p12 chr20: 45,726,581-45,749,938	SPINT5P, HNRNPA1P3, 1 more genes
nsv575163	copy number variation	63	nstd54	human		NCBI36 chr17: 41,525,626-41,648,797 , GRCh37.p13 chr17: 44,176,718-44,293,020 , GRCh37.p13 chr17\|NW_003871086.1: 266,373-349,823 , GRCh38.p12 chr17: 46,092,442-46,215,654 , GRCh38.p12 chr17\|NT_187663.1: 794,550-917,827	LOC107985027, KANSL1-AS1, 1 more genes
nsv571097	copy number variation	1	nstd54	human		NCBI36 chr16: 1,010,148-1,043,096 , GRCh37.p13 chr16: 1,070,147-1,103,095 , GRCh38.p12 chr16: 1,020,147-1,053,095	0
nsv611423	copy number variation	9	nstd54	human		NCBI36 chr8: 62,020,767-62,032,203 , GRCh37.p13 chr8: 61,858,213-61,869,649 , GRCh38.p12 chr8: 60,945,654-60,957,090	0

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HGDP01079 AND nstd54 (9)
dbVar

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