SP52863 AND nstd71 - dbVar - NCBI

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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
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
nsv877298	copy number variation	1	nstd71	human		NCBI36 chr3: 106,207,324-106,223,206 , GRCh37.p13 chr3: 104,724,634-104,740,516 , GRCh38.p12 chr3: 105,005,790-105,021,672	LOC105374023
nsv880577	copy number variation	8	nstd71	human		NCBI36 chr4: 162,058,162-162,109,433 , GRCh37.p13 chr4: 161,838,712-161,889,983 , GRCh38.p12 chr4: 160,917,560-160,968,831	LOC105377513
nsv890721	copy number variation	13	nstd71	human		NCBI36 chr8: 39,331,592-39,509,376 , GRCh37.p13 chr8: 39,212,435-39,390,219 , GRCh38.p12 chr8: 39,354,916-39,532,700	ADAM5, ADAM3A
nsv876428	copy number variation	3	nstd71	human		NCBI36 chr3: 4,046,151-4,156,750 , GRCh37.p13 chr3: 4,071,151-4,181,750 , GRCh38.p12 chr3: 4,029,467-4,140,066	LOC102723512, SUMF1
nsv898873	copy number variation	29	nstd71	human		NCBI36 chr12: 20,899,271-20,907,027 , GRCh37.p13 chr12: 21,008,004-21,015,760 , GRCh38.p12 chr12: 20,855,070-20,862,826	SLCO1B3-SLCO1B7, SLCO1B3
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
nsv903812	copy number variation	6	nstd71	human		NCBI36 chr15: 28,515,105-28,597,366 , GRCh37.p13 chr15: 30,727,813-30,810,074 , GRCh38.p12 chr15: 30,435,610-30,517,871	LOC105376704, MPHOSPH10P3, 1 more genes
nsv903907	copy number variation	31	nstd71	human		NCBI36 chr15: 30,231,488-30,297,802 , GRCh37.p13 chr15: 32,444,196-32,510,510 , GRCh38.p12 chr15: 32,151,995-32,218,309	LOC102724078, CHRNA7, 1 more genes
nsv902761	copy number variation	101	nstd71	human		NCBI36 chr15: 19,031,743-19,212,282 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr15: 20,729,748-21,258,351	POTEB2, MIR5701-1, 22 more genes
nsv903788	copy number variation	4	nstd71	human		NCBI36 chr15: 28,274,337-28,492,124 , GRCh37.p13 chr15: 30,487,045-30,704,832 , GRCh38.p12 chr15: 30,194,842-30,412,629	CHRFAM7A, DNM1P29, 9 more genes
nsv884258	copy number variation	146	nstd71	human		NCBI36 chr6: 31,388,306-31,398,785 , GRCh37.p13 chr6\|NT_167249.1: 2,614,037-2,624,528 , GRCh37.p13 chr6: 31,280,327-31,290,806 , GRCh38.p12 chr6: 31,312,550-31,323,029 , GRCh38.p12 chr6\|NT_167249.2: 2,614,739-2,625,230	0
nsv872501	copy number variation	2	nstd71	human		NCBI36 chr1: 160,393,068-160,634,278 , GRCh37.p13 chr1: 162,126,444-162,367,654 , GRCh38.p12 chr1: 162,156,654-162,397,864	SH2D1B, RNA5SP61, 6 more genes
nsv884762	copy number variation	15	nstd71	human		NCBI36 chr6: 32,549,370-32,563,460 , GRCh37.p13 chr6: 32,441,392-32,455,482 , GRCh38.p12 chr6: 32,473,615-32,487,705	0

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