dnai4[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
nsv1398228	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 67,327,908-67,519,596 , GRCh38.p12 chr1: 66,862,225-67,053,913	DNAI4, SLC35D1, 1 more genes
nsv3901546	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 59,057,865-86,336,882 , GRCh37 chr1: 59,285,277-86,564,294 , GRCh38 chr1: 58,819,605-86,098,611	DNAI4, ROR1, 333 more genes
nsv3886551	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 64,321,264-88,153,669 , GRCh38.p12 chr1: 63,855,593-87,687,986	DNAI4, RNU6-1102P, 291 more genes
nsv3884583	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 61,351,024-79,583,933 , GRCh38.p12 chr1: 60,885,352-79,118,248	DNAI4, MIR7156, 243 more genes
nsv3903468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 59,870,760-76,969,150 , GRCh37 chr1: 60,098,172-77,196,562 , GRCh38 chr1: 59,632,500-76,730,877	DNAI4, WLS, 219 more genes
nsv3909388	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 57,816,246-71,791,607 , GRCh38 chr1: 57,350,574-71,325,924 , NCBI36 chr1: 57,588,834-71,564,195	DNAI4, RNU6-1031P, 193 more genes
nsv4453663	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 59,922,631-72,058,653 , GRCh38.p12 chr1: 59,456,959-71,592,970	DNAI4, RNU6-387P, 170 more genes
nsv3901841	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 59,760,856-71,578,052 , NCBI36 chr1: 59,999,116-71,816,323 , GRCh37 chr1: 60,226,528-72,043,735	DNAI4, MIR3116-2, 169 more genes
nsv3901058	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 60,473,800-70,944,955 , NCBI36 chr1: 60,712,060-71,183,226 , GRCh37 chr1: 60,939,472-71,410,638	DNAI4, UBE2U, 150 more genes
nsv3891330	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 59,057,865-69,345,379 , GRCh37 chr1: 59,285,277-69,572,791 , GRCh38 chr1: 58,819,605-69,107,108	DNAI4, RPS7P4, 148 more genes
nsv3908260	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 67,330,808-77,589,066 , NCBI36 chr1: 67,103,396-77,361,654 , GRCh38 chr1: 66,865,125-77,123,381	DNAI4, RNA5SP50, 119 more genes
nsv4449847	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 66,868,168-77,106,425 , GRCh38.p12 chr1: 66,402,485-76,640,740	DNAI4, GNG12-AS1, 118 more genes
nsv7095627	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 61,548,464-67,861,772 , GRCh38.p12 chr1: 61,082,792-67,396,089	DNAI4, ALG6, 94 more genes
nsv7095538	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 65,299,551-67,861,772 , GRCh38.p12 chr1: 64,833,868-67,396,089	DNAI4, MRPS21P1, 36 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	DNAI4, MARK1, 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	DNAI4, SNAP47, 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	DNAI4, RNU1-153P, 4887 more genes
nsv3896927	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 53,061,024-77,233,450 , GRCh38 chr1: 52,595,352-76,767,765 , NCBI36 chr1: 52,833,612-77,006,038	DNAI4, LOC105378770, 346 more genes
nsv3907158	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 64,072,618-75,518,432 , NCBI36 chr1: 64,310,878-75,756,705 , GRCh37 chr1: 64,538,290-75,984,117	DNAI4, SGIP1, 134 more genes
nsv3879648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 62,434,799-71,656,180 , GRCh38.p12 chr1: 61,969,127-71,190,497	DNAI4, MRPS21P1, 142 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 29

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Number of Variants: 20

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Supplemental Content

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Search details

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