"nstd102"[study] AND "maternal"[Origin] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3905990	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,650,185-31,972,259 , NCBI36 chrX: 31,560,106-31,882,180 , GRCh38 chrX: 31,632,068-31,954,142	DMD
nsv3920457	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 70,206,515-70,493,590 , NCBI36 chr7: 69,309,437-69,596,512 , GRCh37 chr7: 69,671,501-69,958,576	AUTS2
nsv1398664	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 51,005,771-51,246,088 , GRCh38.p12 chr2: 50,778,633-51,018,950	NRXN1
nsv3873698	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 103,016,481-103,177,263 , GRCh38 chr11: 103,145,752-103,306,534	DYNC2H1
nsv3906312	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 50,851,255-50,995,129 , NCBI36 chr2: 50,931,897-51,075,771 , GRCh37 chr2: 51,078,393-51,222,267	NRXN1
nsv3923087	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 127,805,264-127,928,641 , GRCh38 chr5: 128,441,672-128,565,049 , GRCh37 chr5: 127,777,365-127,900,742	FBN2
nsv3874415	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 15,570,188-15,674,295 , GRCh37 chr8: 15,427,697-15,531,804	TUSC3
nsv3905740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,449,215-31,543,991 , NCBI36 chrX: 31,359,136-31,453,912 , GRCh38 chrX: 31,431,098-31,525,874	DMD
nsv6315379	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 132,703,748-132,794,615 , GRCh38.p12 chrX: 133,569,720-133,660,587	GPC3
nsv3892599	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 51,142,849-51,226,229 , NCBI36 chr2: 50,996,353-51,079,733 , GRCh38 chr2: 50,915,711-50,999,091	NRXN1
nsv3913979	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 31,792,077-31,854,939 , GRCh38.p12 chrX: 31,773,960-31,836,822	DMD
nsv3896305	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 20,173,087-20,235,708 , GRCh38 chrX: 20,154,969-20,217,590 , NCBI36 chrX: 20,083,008-20,145,629	RPS6KA3
nsv4716480	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 78,152,047-78,188,346 , GRCh37.p13 chr16: 78,185,944-78,222,243	WWOX
nsv7099030	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 20,041,466-20,075,200 , GRCh37.p13 chr22: 20,028,989-20,062,723	TANGO2
nsv6289906	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 108,151,766-108,183,226 , GRCh37.p13 chr11: 108,022,493-108,053,953	NPAT
nsv4347287	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 200,213,361-200,233,633 , GRCh38.p12 chr2: 199,348,638-199,368,910	SATB2
nsv3887384	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 10,182,428-10,201,480 , GRCh38.p12 chrX: 10,214,388-10,233,440	CLCN4
nsv3872571	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 108,915,663-108,933,582 , GRCh38.p12 chrX: 109,672,434-109,690,353	ACSL4
nsv3914470	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 147,030,199-147,046,357 , GRCh38.p12 chrX: 147,948,679-147,964,837	FMR1
nsv6289901	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 44,300,489-44,312,646 , GRCh38.p12 chr5: 44,300,387-44,312,544	FGF10

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Organism

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Has Clinical Interpretation

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Items: 1 to 20 of 1945

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Number of Variants: 20

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