MS14905 AND nstd71 - 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
nsv884822	copy number variation	2547	nstd71	human		NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715	HLA-DRB5
nsv890813	copy number variation	21	nstd71	human		NCBI36 chr8: 39,408,900-39,497,557 , GRCh37.p13 chr8: 39,289,743-39,378,400 , GRCh38.p12 chr8: 39,432,224-39,520,881	ADAM3A
nsv893231	copy number variation	140	nstd71	human		NCBI36 chr9: 43,594,114-43,641,682 , GRCh37.p13 chr9: 43,654,118-43,701,686 , GRCh38.p12 chr9: 42,112,703-42,160,271	CNTNAP3B
nsv908409	copy number variation	61	nstd71	human		NCBI36 chr17: 41,781,845-41,943,845 , GRCh37.p13 chr17: 44,426,089-44,588,529 , GRCh38.p12 chr17: 46,348,723-46,511,163	LRRC37A2, NSFP1, 2 more genes
nsv911369	copy number variation	219	nstd71	human		NCBI36 chr19: 20,404,485-20,520,617 , GRCh37.p13 chr19: 20,612,645-20,728,777 , GRCh37.p13 chr19\|NW_003571053.2: 347,092-463,224 , GRCh38.p12 chr19: 20,429,839-20,545,971	ZNF737, LOC105372316, 2 more genes
nsv879310	copy number variation	1929	nstd71	human		NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558	LOC100422402, LOC100132651, 2 more genes
nsv911912	copy number variation	43	nstd71	human		NCBI36 chr19: 48,060,801-48,160,500 , GRCh37.p13 chr19: 43,368,961-43,468,660 , GRCh38.p12 chr19: 42,864,809-42,964,508	CEACAMP7, PSG1, 2 more genes
nsv893278	copy number variation	148	nstd71	human		NCBI36 chr9: 43,616,717-44,683,090 , GRCh37.p13 chr9: 43,676,721-44,743,094 , GRCh38.p12 chr9: 41,912,139-42,974,549	RBM17P3, RNU6-599P, 30 more genes

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