OSC3935 AND nstd224 - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6630626	copy number variation	240	nstd224	human		GRCh37 chr5: 97,061,761-97,096,042 , GRCh38.p12 chr5: 97,726,057-97,760,338	LOC391813
nsv6626714	copy number variation	62	nstd224	human		GRCh37 chr20: 58,440,438-58,461,886 , GRCh38.p12 chr20: 59,865,383-59,886,831	SYCP2
nsv6622266	copy number variation	11	nstd224	human		GRCh37 chr14: 24,435,557-24,464,590 , GRCh38.p12 chr14: 23,966,348-23,995,381 , GRCh38.p12 chr14\|NW_018654722.1: 267,326-301,715	DHRS4, DHRS4L2
nsv6624176	copy number variation	1	nstd224	human		GRCh37 chr18: 65,383,418-65,404,933 , GRCh38.p12 chr18: 67,716,181-67,737,696	DSEL-AS1, LOC105372173
nsv6624844	copy number variation	645	nstd224	human		GRCh37 chr19: 20,630,360-20,715,228 , GRCh38.p12 chr19: 20,447,554-20,532,422	ZNF737, LOC105372316, 1 more genes
nsv6633226	copy number variation	78	nstd224	human		GRCh37 chr9: 140,166,981-140,196,334 , GRCh38.p12 chr9: 137,272,529-137,301,882	NRARP, TOR4A, 1 more genes
nsv6626073	copy number variation	2	nstd224	human		GRCh37 chr1: 196,794,652-196,918,615 , GRCh38.p12 chr1: 196,825,522-196,949,485	CFHR2, LOC100996886, 3 more genes
nsv6625130	copy number variation	188	nstd224	human		GRCh37 chr19: 43,344,686-43,528,980 , GRCh38.p12 chr19: 42,840,534-43,024,828	CEACAMP7, PSG1, 4 more genes
nsv6630136	copy number variation	1	nstd224	human		GRCh37 chr5: 178,770,485-179,025,550 , GRCh38.p12 chr5: 179,343,484-179,598,549 , GRCh38.p12 chr5\|NW_016107298.1: 108,191-364,823	ADAMTS2, RUFY1, 7 more genes
nsv6631973	copy number variation	4	nstd224	human		GRCh37 chr7: 57,481,104-57,621,951 , GRCh38.p12 chr7: 57,421,392-57,562,245	ZNF716, SAPCD2P2, 4 more genes
nsv6620856	copy number variation	2	nstd224	human		GRCh37 chr10: 90,477,590-90,596,859 , GRCh38.p12 chr10: 88,717,833-88,837,102	ANKRD22, LIPM, 4 more genes
nsv6630183	copy number variation	48	nstd224	human		GRCh37 chr4: 9,371,116-9,485,300 , GRCh38.p12 chr4: 9,369,390-9,483,653	OR7E84P, USP17L6P, 7 more genes
nsv6622128	copy number variation	1	nstd224	human		GRCh37 chr13: 24,771,519-25,020,887 , GRCh38.p12 chr13: 24,197,381-24,446,749	CEND1P2, PARP4, 8 more genes
nsv6632147	copy number variation	132	nstd224	human		GRCh37 chr7: 44,935-67,365 , GRCh38.p12 chr7: 44,935-67,365 , GRCh38.p12 chr7\|NT_187558.1: 1,034-23,464 , GRCh38.p12 chr7\|NT_187653.1: 37,256-59,686	0

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