"nstd166"[study] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv4136077	copy number variation	1	nstd166	human	GRCh37.p13 chr6: 62,437,659-63,122,645 , GRCh38.p12 chr6: 61,727,754-62,412,740	KHDRBS2
nsv4132066	copy number variation	1	nstd166	human	GRCh37.p13 chr5: 120,218,512-120,778,633 , GRCh38.p12 chr5: 120,882,817-121,442,938	LOC102467226
nsv4033869	copy number variation	1	nstd166	human	GRCh37.p13 chrX: 94,174,949-94,722,850 , GRCh38.p12 chrX: 94,919,950-95,467,851	MIR548M
nsv4221411	copy number variation	1	nstd166	human	GRCh37.p13 chr14: 42,640,939-43,137,520 , GRCh38.p12 chr14: 42,171,736-42,668,317	LOC100420765
nsv4062593	copy number variation	1	nstd166	human	GRCh37.p13 chr1: 191,594,660-192,054,701 , GRCh38.p12 chr1: 191,625,530-192,085,571	LINC02770
nsv4194179	copy number variation	1	nstd166	human	GRCh37.p13 chr11: 25,148,708-25,605,723 , GRCh38.p12 chr11: 25,127,162-25,584,177	LOC100130747
nsv4146514	copy number variation	1	nstd166	human	GRCh37.p13 chr6: 162,168,587-162,623,384 , GRCh38.p12 chr6: 161,747,555-162,202,352	PRKN
nsv4178416	copy number variation	1	nstd166	human	GRCh37.p13 chr10: 55,223,908-55,665,774 , GRCh38.p12 chr10: 53,464,148-53,906,014	PCDH15
nsv4174859	copy number variation	1	nstd166	human	GRCh37.p13 chr9: 11,867,966-12,273,398 , GRCh38.p12 chr9: 11,867,966-12,273,398	LOC105375976
nsv4181320	copy number variation	1	nstd166	human	GRCh37.p13 chr10: 56,842,876-57,247,859 , GRCh38.p12 chr10: 55,083,116-55,488,099	PCDH15
nsv4127866	copy number variation	1	nstd166	human	GRCh37.p13 chr5: 98,932,732-99,324,872 , GRCh38.p12 chr5: 99,597,028-99,989,168	CRLF3P2
nsv4035298	copy number variation	1	nstd166	human	GRCh37.p13 chrX: 98,697,539-99,082,605 , GRCh38.p12 chrX: 99,442,541-99,827,607	XRCC6P5
nsv4116602	copy number variation	1	nstd166	human	GRCh37.p13 chr5: 19,072,028-19,453,172 , GRCh38.p12 chr5: 19,071,919-19,453,063	HSPD1P15
nsv4190943	copy number variation	1	nstd166	human	GRCh37.p13 chr9: 23,099,440-23,476,866 , GRCh38.p12 chr9: 23,099,441-23,476,868
nsv4072203	copy number variation	1	nstd166	human	GRCh37.p13 chr2: 41,530,160-41,894,128 , GRCh38.p12 chr2: 41,303,020-41,666,988	LOC105374506
nsv4094819	copy number variation	1	nstd166	human	GRCh37.p13 chr4: 60,391,515-60,752,646 , GRCh38.p12 chr4: 59,525,797-59,886,928	RNU6-1325P
nsv4060698	copy number variation	1	nstd166	human	GRCh37.p13 chr1: 189,239,878-189,599,404 , GRCh38.p12 chr1: 189,270,747-189,630,274	LOC105371657
nsv4175795	copy number variation	1	nstd166	human	GRCh37.p13 chr9: 11,859,228-12,217,273 , GRCh38.p12 chr9: 11,859,228-12,217,273	LOC105375976
nsv4111296	copy number variation	1	nstd166	human	GRCh37.p13 chr4: 121,300,511-121,658,459 , GRCh38.p12 chr4: 120,379,356-120,737,304	PRDM5
nsv4187516	copy number variation	1	nstd166	human	GRCh37.p13 chr10: 56,658,500-57,013,519 , GRCh38.p12 chr10: 54,898,740-55,253,759	PCDH15

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Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

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Subject Phenotype Status

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Items: 1 to 20 of 304733

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Number of Variants: 20

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Supplemental Content

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