atad1[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
nsv4456721	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 89,492,635-89,531,333 , GRCh38.p12 chr10: 87,732,878-87,771,576	ATAD1, PAPSS2
nsv7093897	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 89,468,933-89,574,356 , GRCh38.p12 chr10: 87,709,176-87,814,599	ATAD1, PAPSS2
nsv3873241	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 89,589,557-89,642,550 , GRCh38.p12 chr10: 87,829,800-87,882,793 , GRCh38.p12 chr10\|NW_013171807.1: 45,622-98,616	ATAD1, PTEN, 3 more genes
nsv4455430	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 89,456,983-89,615,124 , GRCh38.p12 chr10: 87,697,226-87,855,367	ATAD1, PAPSS2, 2 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	ATAD1, RNU7-12P, 1876 more genes
nsv3920295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422	ATAD1, EIF2S2P3, 895 more genes
nsv6637542	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 82,595,472-93,542,416 , GRCh38.p12 chr10: 80,835,716-91,782,659	ATAD1, IFIT6P, 166 more genes
nsv3891568	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 83,379,241-93,219,169 , GRCh38.p12 chr10: 81,619,485-91,459,412	ATAD1, NAPGP1, 157 more genes
nsv6634458	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 83,533,660-91,913,077 , GRCh38.p12 chr10: 81,773,904-90,153,320	ATAD1, IFIT5, 140 more genes
nsv4729624	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 88,685,387-92,144,296 , GRCh38.p12 chr10: 86,925,630-90,384,539	ATAD1, LOC105378414, 84 more genes
nsv6291116	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 87,232,436-89,649,679 , GRCh38.p12 chr10: 85,472,679-87,889,922	ATAD1, CFL1P1, 48 more genes
nsv3885274	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 87,887,949-90,299,688 , GRCh37.p13 chr10: 87,897,969-90,309,708 , GRCh38.p12 chr10: 86,138,212-88,549,951	ATAD1, GRID1, 50 more genes
nsv3880796	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 87,983,839-89,527,417 , GRCh37.p13 chr10: 87,993,859-89,537,437 , GRCh38.p12 chr10: 86,234,102-87,777,680	ATAD1, RN7SL733P, 38 more genes
nsv7093895	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 88,428,449-89,725,229 , GRCh38.p12 chr10: 86,668,692-87,965,472	ATAD1, LOC105378410, 33 more genes
nsv4683983	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 89,311,839-90,528,685 , GRCh38.p12 chr10: 87,552,082-88,768,928	ATAD1, MINPP1, 22 more genes
nsv4683124	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 88,514,773-89,725,321 , GRCh38.p12 chr10: 86,755,016-87,965,564	ATAD1, NUTM2A, 32 more genes
nsv4454138	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 86,755,016-87,965,482 , GRCh37 chr10: 88,514,773-89,725,239	ATAD1, PAPSS2, 32 more genes
nsv4453333	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 88,598,623-89,725,239 , GRCh38 chr10: 86,838,866-87,965,482	ATAD1, PTEN, 32 more genes
nsv3876950	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 88,649,809-89,725,239 , GRCh38.p12 chr10: 86,890,052-87,965,482	ATAD1, LOC112268064, 31 more genes
nsv5672610	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 88,683,123-89,725,321 , GRCh38.p12 chr10: 86,923,366-87,965,564	ATAD1, FAM245A, 30 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 33

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Number of Variants: 20

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