OSC3737 AND nstd224 - 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
nsv6627960	copy number variation	4	nstd224	human		GRCh37 chr2: 52,407,060-52,578,154 , GRCh38.p12 chr2: 52,179,922-52,351,016	NRXN1-DT
nsv6632210	copy number variation	1	nstd224	human		GRCh37 chr7: 85,814,138-85,871,095 , GRCh38.p12 chr7: 86,184,822-86,241,779	SOCS5P1
nsv6633047	copy number variation	17	nstd224	human		GRCh37 chr8: 39,644,542-39,678,652 , GRCh38.p12 chr8: 39,787,023-39,821,133 , GRCh38.p12 chr8\|NT_187577.1: 537,657-571,769	ADAM2
nsv6633275	copy number variation	3	nstd224	human		GRCh37 chr8: 82,736,033-82,752,291 , GRCh38.p12 chr8: 81,823,798-81,840,056	SNX16
nsv6621231	copy number variation	29	nstd224	human		GRCh37 chr11: 95,569,341-95,621,376 , GRCh38.p12 chr11: 95,836,177-95,888,212	MTMR2, RNA5SP345
nsv6628018	copy number variation	15	nstd224	human		GRCh37 chr2: 239,038,829-239,049,729 , GRCh38.p12 chr2: 238,130,188-238,141,088	ESPNL, KLHL30
nsv6620147	copy number variation	3	nstd224	human		GRCh37 chr10: 46,968,668-47,000,252 , GRCh38.p12 chr10: 46,549,365-46,580,949	SYT15, SYT15-AS1, 1 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
nsv6630221	copy number variation	102	nstd224	human		GRCh37 chr5: 113,160,490-113,171,928 , GRCh38.p12 chr5: 113,824,793-113,836,231	0
nsv6634036	copy number variation	2	nstd224	human		GRCh37 chrX: 103,200,296-103,295,458 , GRCh38.p12 chrX: 103,945,722-104,040,891	H2BW1, H2BW2, 4 more genes
nsv6626452	copy number variation	11	nstd224	human		GRCh37 chr1: 41,347,228-41,378,076 , GRCh38.p12 chr1: 40,881,556-40,912,404	0

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