cnih2[All Fields] AND 1[has_clinical] - 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
nsv4728731	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 224,442,473-224,794,913 , GRCh38.p12 chr1: 224,254,771-224,607,211	NVL, CNIH4, 7 more genes
nsv7148187	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 224,304,638-224,434,886 , GRCh37.p13 chr1: 224,492,340-224,622,588	NVL, CNIH4, 4 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	CNIH2, FAUP4, 2031 more genes
nsv4674115	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 223,653,722-234,591,807 , GRCh38.p12 chr1: 223,480,380-234,456,061	LOC105373163, CDC42BPA, 258 more genes
nsv4674157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 222,641,389-228,137,574 , GRCh38.p12 chr1: 222,468,047-227,949,873	SRP9, AKR1B1P1, 123 more genes
nsv3908695	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 221,587,658-226,810,656 , GRCh38 chr1: 223,347,693-228,556,332 , GRCh37 chr1: 223,521,035-228,744,033	SNAP47, OBSCN-AS1, 137 more genes
nsv4728176	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 222,605,125-224,696,628 , GRCh38.p12 chr1: 222,431,783-224,508,926	SEPTIN7P13, LOC101927164, 52 more genes
nsv3921639	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 65,265,478-67,229,716 , GRCh37 chr11: 65,508,902-67,473,140 , GRCh38 chr11: 65,741,431-67,705,669	CNIH2, MIR6860, 106 more genes
nsv6309121	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 64,522,783-66,283,694 , GRCh38.p12 chr11: 64,755,311-66,516,223	CNIH2, SF3B2, 124 more genes
nsv5200338	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 223,552,998-224,761,890 , GRCh38.p12 chr1: 223,379,656-224,574,188	LOC105373025, CAPN2, 32 more genes
nsv4346523	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 224,340,881-225,147,932 , GRCh38.p12 chr1: 224,153,179-224,960,230	RNU6-1008P, MIR4742, 18 more genes
nsv6315349	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 224,432,682-225,142,704 , GRCh38.p12 chr1: 224,244,980-224,955,002	DNAJB6P6, CNIH3, 13 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	MARK1, LINC02766, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	SNAP47, STK40, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	RNU1-153P, MIR3917, 4887 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	CNIH2, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	CNIH2, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	CNIH2, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	CNIH2, PYGM, 2125 more genes
nsv4450583	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 182,388,773-249,111,240 , GRCh38.p12 chr1: 182,419,638-248,817,041	RGS18, LINC02257, 1186 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 59

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Number of Variants: 20

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Supplemental Content

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