setd2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6315036	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr3: 47,142,709-47,168,492 , GRCh37.p13 chr3: 47,184,199-47,209,982	SETD2, KIF9-AS1
nsv5381363	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 47,205,324-47,205,434 , GRCh38.p12 chr3: 47,163,834-47,163,944	SETD2, KIF9-AS1
nsv6315166	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376	SETD2, TMEM89, 129 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	SETD2, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	SETD2, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	SETD2, RPL23AP49, 2875 more genes
nsv4347762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589	SETD2, UQCRC1, 291 more genes
nsv3921797	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 45,896,379-50,762,357 , GRCh38 chr3: 45,879,883-50,749,922 , GRCh37 chr3: 45,921,375-50,787,353	SETD2, RBM5-AS1, 185 more genes
nsv3883164	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 37,028,313-49,929,220 , GRCh38.p12 chr3: 36,986,822-49,891,787	SETD2, ACAA1, 344 more genes
nsv4453008	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 47,068,320-47,472,020 , GRCh38.p12 chr3: 47,026,830-47,430,530	SETD2, SCAP, 7 more genes
nsv3874579	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 47,069,054-47,468,261 , GRCh38.p12 chr3: 47,027,564-47,426,771	SETD2, PTPN23, 7 more genes
nsv7097200	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 47,079,136-47,454,675 , GRCh38.p12 chr3: 47,037,646-47,413,185	SETD2, SNORD13P3, 6 more genes
nsv6637062	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 47,188,373-47,350,231 , GRCh38.p12 chr3: 47,146,883-47,308,741	SETD2, KLHL18, 4 more genes
nsv3918364	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 47,155,984-47,313,701 , GRCh37.p13 chr3: 47,180,980-47,338,697 , GRCh38.p12 chr3: 47,139,490-47,297,207	SETD2, KIF9, 4 more genes
nsv6636386	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 47,188,373-47,338,349 , GRCh38.p12 chr3: 47,146,883-47,296,859	SETD2, KIF9, 4 more genes
nsv7096805	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318	SETD2, SNORA94, 120 more genes

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