OSC2301 AND nstd224 - dbVar - NCBI

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Items: 10

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Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6623886	copy number variation	1	nstd224	human		GRCh37 chr16: 6,993,055-7,021,004 , GRCh38.p12 chr16: 6,943,054-6,971,003	RBFOX1
nsv6628654	copy number variation	115	nstd224	human		GRCh37 chr3: 151,514,590-151,545,958 , GRCh38.p12 chr3: 151,796,802-151,828,170	AADAC, AADACL2-AS1
nsv6630396	copy number variation	144	nstd224	human		GRCh37 chr5: 32,108,076-32,151,119 , GRCh38.p12 chr5: 32,107,970-32,151,013	PDZD2, GOLPH3
nsv6628155	copy number variation	1	nstd224	human		GRCh37 chr2: 82,493,580-82,527,769 , GRCh38.p12 chr2: 82,266,456-82,300,645	LYARP1, RNU6-685P
nsv6633392	copy number variation	1	nstd224	human		GRCh37 chr9: 116,118,952-116,137,673 , GRCh38.p12 chr9: 113,356,672-113,375,393	HDHD3, BSPRY
nsv6628116	copy number variation	277	nstd224	human		GRCh37 chr2: 38,956,836-38,972,328 , GRCh38.p12 chr2: 38,729,694-38,745,186	SRSF7, GALM
nsv6625364	copy number variation	3	nstd224	human		GRCh37 chr1: 12,887,332-12,921,311 , GRCh38.p12 chr1: 12,827,473-12,861,456 , GRCh38.p12 chr1\|NW_012132914.1: 8,986-42,969	PRAMEF11, PRAMEF30P, 2 more genes
nsv6627726	copy number variation	214	nstd224	human		GRCh37 chr2: 179,300,979-179,315,726 , GRCh38.p12 chr2: 178,436,252-178,450,999	PRKRA, PJVK, 1 more genes
nsv6630107	copy number variation	584	nstd224	human		GRCh37 chr5: 140,223,185-140,238,124 , GRCh38.p12 chr5: 140,843,600-140,858,539	PCDHA4, PCDHA1, 9 more genes
nsv6631986	copy number variation	1	nstd224	human		GRCh37 chr7: 65,202,326-65,326,821 , GRCh38.p12 chr7: 65,737,334-65,861,834	LOC84214, LINC03006, 6 more genes

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