"nstd39"[study] AND "copy number loss"[variant_type] - dbVar - NCBI

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv482216	copy number variation	1	nstd39	human		NCBI35 chr19: 15,423,438-15,436,382 , GRCh37.p13 chr19: 15,562,438-15,575,382 , GRCh38.p12 chr19: 15,451,627-15,464,571	RASAL3
nsv482209	copy number variation	1	nstd39	human		NCBI35 chr19: 2,792,482-2,805,033 , GRCh37.p13 chr19: 2,841,482-2,854,033 , GRCh38.p12 chr19: 2,841,484-2,854,035	ZNF555
nsv482204	copy number variation	1	nstd39	human		NCBI35 chr17: 44,390,917-44,400,954 , GRCh37.p13 chr17: 47,035,918-47,045,955 , GRCh38.p12 chr17: 48,958,556-48,968,593	GIP
nsv482098	copy number variation	1	nstd39	human		NCBI35 chr6: 114,285,220-114,291,345 , GRCh37.p13 chr6: 114,178,527-114,184,652 , GRCh38.p12 chr6: 113,857,348-113,863,475	MARCKS
nsv482046	copy number variation	1	nstd39	human		NCBI35 chr19: 52,973,654-52,979,751 , GRCh37.p13 chr19: 48,281,842-48,287,939 , GRCh38.p12 chr19: 47,778,585-47,784,682	SELENOW
nsv482125	copy number variation	1	nstd39	human		NCBI35 chr1: 148,939,144-148,944,777 , GRCh37.p13 chr1: 152,126,071-152,131,704 , GRCh38.p12 chr1: 152,153,595-152,159,228	RPTN
nsv482136	copy number variation	1	nstd39	human		NCBI35 chr1: 157,998,160-158,002,111 , GRCh37.p13 chr1: 161,185,087-161,189,038 , GRCh38.p12 chr1: 161,215,297-161,219,248	FCER1G
nsv482163	copy number variation	1	nstd39	human		NCBI35 chr11: 125,121,398-125,124,952 , GRCh37.p13 chr11: 125,616,188-125,619,742 , GRCh38.p12 chr11: 125,746,293-125,749,847	PATE1
nsv482091	copy number variation	1	nstd39	human		NCBI35 chr5: 150,254,157-150,264,584 , GRCh37.p13 chr5: 150,273,964-150,284,391 , GRCh38.p12 chr5: 150,894,402-150,904,829	ZNF300, IRGM
nsv482156	copy number variation	1	nstd39	human		NCBI35 chr11: 3,643,393-3,649,190 , GRCh37.p13 chr11: 3,686,817-3,692,614 , GRCh38.p12 chr11: 3,665,587-3,671,384	ART1, CHRNA10
nsv482095	copy number variation	1	nstd39	human		NCBI35 chr6: 41,225,322-41,230,048 , GRCh37.p13 chr6: 41,117,344-41,122,070 , GRCh38.p12 chr6: 41,149,606-41,154,332	TREML1, LOC105375056
nsv482075	copy number variation	1	nstd39	human		NCBI35 chr22: 22,700,693-22,708,838 , GRCh37.p13 chr22: 24,376,139-24,384,284 , GRCh38.p12 chr22\|NT_187633.1: 270,314-278,459	GSTT1, GSTTP2, 1 more genes
nsv482200	copy number variation	1	nstd39	human		NCBI35 chr17: 23,959,109-23,965,338 , GRCh37.p13 chr17: 26,934,982-26,941,211 , GRCh38.p12 chr17: 28,607,964-28,614,193	BLTP2, RSKR, 1 more genes
nsv482162	copy number variation	1	nstd39	human		NCBI35 chr11: 111,284,560-111,287,683 , GRCh37.p13 chr11\|NW_003871080.1: 160,617-163,740 , GRCh37.p13 chr11: 111,779,350-111,782,473 , GRCh38.p12 chr11: 111,908,626-111,911,749	CRYAB, HSPB2, 1 more genes
nsv482171	copy number variation	1	nstd39	human		NCBI35 chr14: 23,978,814-23,981,847 , GRCh37.p13 chr14: 24,908,974-24,912,007 , GRCh38.p12 chr14: 24,439,768-24,442,801	KHNYN, SDR39U1, 1 more genes

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